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Molecular Approaches to Gynecological Cancers: Biomarkers and Targeted Therapeutic Pathways

Year 2026, Volume: 7 Issue: 1 , 86 - 104 , 27.03.2026
https://doi.org/10.46871/eams.1868915
https://izlik.org/JA64SJ72BF

Abstract

Gynecological cancers, including ovarian, endometrial, and cervical malignancies, represent a heterogeneous group of tumors characterized by distinct clinical behaviors and complex molecular properties. Advances in molecular oncology have substantially reshaped the understanding of gynecological carcinogenesis, revealing that dysregulation of tumor suppressor genes, DNA damage repair pathways, oncogenic signaling cascades, and virus-driven mechanisms critically influence disease initiation, progression, and therapeutic response. In ovarian cancer, alterations in homologous recombination repair, TP53 mutations, and aberrant activation of MAPK and PI3K/AKT signaling pathways have enabled molecular stratification and the successful implementation of targeted therapies. Endometrial cancer exemplifies the transition toward molecular classification, with POLE exonuclease domain mutations, mismatch repair deficiency, and copy number alterations defining biologically and clinically distinct subgroups with divergent prognostic outcomes. Cervical cancer represents a unique virus associated malignancy in which persistent high risk human papillomavirus infection drives oncogenesis through disruption of cell cycle regulatory pathways, providing a robust biological basis for molecular diagnostics and prevention strategies. This review comprehensively summarizes the current knowledge of key molecular biomarkers and signaling pathways involved in gynecological cancers, including CA-125, mismatch repair deficiency, TP53, HER2, BRCA-associated DNA repair mechanisms, POLE mutations, WNT/β-catenin signaling, and HPV-related molecular alterations. Furthermore, the clinical implications of these molecular insights for diagnosis, prognosis, risk stratification, and personalized therapeutic approaches are discussed. In conclusion, integration of molecular profiling into clinical practice represents a critical step toward precision medicine in gynecological oncology, offering the potential to improve patient outcomes through biomarker-driven diagnosis and targeted treatment strategies.

References

  • 1. Pietras C, Khoo T, Karlin D. Updates in palliative care of patients with gynecologic malignancies in 2026: early integration, resource models, and emerging therapies. Current opinion in obstetrics & gynecology. 2026;38(1):1-5.
  • 2. Rashid H, Ullah A, Ahmad S, Aljahdali SM, Waheed Y, Shaker B, et al. Identification of Novel Genes and Pathways of Ovarian Cancer Using a Comprehensive Bioinformatic Framework. Applied biochemistry and biotechnology. 2024;196(6):3056-75.
  • 3. Caruso G, Weroha SJ, Cliby W. Ovarian Cancer: A Review. Jama. 2025;334(14):1278-91.
  • 4. Anca-Stanciu MB, Manu A, Olinca MV, Coroleuca C, Comandasu DE, Coroleuca CA, et al. Comprehensive Review of Endometrial Cancer: New Molecular and FIGO Classification and Recent Treatment Changes. Journal of clinical medicine. 2025;14(4).
  • 5. Sahasrabuddhe VV. Cervical Cancer: Precursors and Prevention. Hematology/oncology clinics of North America. 2024;38(4):771-81.
  • 6. Ullah A, Chen Y, Shen Y, Shen B. Chemotherapy as a double-edged sword: Modulation of tumor-associated cytokine and chemokine responses in ovarian cancer. International journal of cancer. 2026;158(5):1141-55.
  • 7. Shin KH, Kim HH, Kwon BS, Suh DS, Joo JK, Kim KH. Clinical Usefulness of Cancer Antigen (CA) 125, Human Epididymis 4, and CA72-4 Levels and Risk of Ovarian Malignancy Algorithm Values for Diagnosing Ovarian Tumors in Korean Patients With and Without Endometriosis. Annals of laboratory medicine. 2020;40(1):40-7.
  • 8. Teh BH, Yong SL, Sim WW, Lau KB, Suharjono HN. Evaluation in the predictive value of serum human epididymal protein 4 (HE4), cancer antigen 125 (CA 125) and a combination of both in detecting ovarian malignancy. Hormone molecular biology and clinical investigation. 2018;35(1).
  • 9. Chen F, Shen J, Wang J, Cai P, Huang Y. Clinical analysis of four serum tumor markers in 458 patients with ovarian tumors: diagnostic value of the combined use of HE4, CA125, CA19-9, and CEA in ovarian tumors. Cancer management and research. 2018;10:1313-8.
  • 10. Ghose A, McCann L, Makker S, Mukherjee U, Gullapalli SVN, Erekkath J, et al. Diagnostic biomarkers in ovarian cancer: advances beyond CA125 and HE4. Therapeutic advances in medical oncology. 2024;16:17588359241233225.
  • 11. Sameer AS, Nissar S, Fatima K. Mismatch repair pathway: molecules, functions, and role in colorectal carcinogenesis. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation. 2014;23(4):246-57.
  • 12. Carethers JM, Stoffel EM. Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancer. World journal of gastroenterology. 2015;21(31):9253-61.
  • 13. Eroglu S, Birsenogul I, Bowen AP, Doyle JF, Pupkin SE, Villar J, et al. Lynch Syndrome in Focus: A Multidisciplinary Review of Cancer Risk, Clinical Management, and Special Populations. Cancers. 2025;17(24).
  • 14. Akbari MR, Zhang S, Cragun D, Lee JH, Coppola D, McLaughlin J, et al. Correlation between germline mutations in MMR genes and microsatellite instability in ovarian cancer specimens. Familial cancer. 2017;16(3):351-5.
  • 15. Kruckel A, Gocke J, Horner M, Keller K, Muller C, Bruckner L, et al. Genetic tumor syndromes in female cancer: insights into inherited cancer predisposition and clinical implications. Archives of gynecology and obstetrics. 2026;313(1):38.
  • 16. Kauppinen AK, Olkinuora AP, Mecklin JP, Peltomaki PT. Molecular analysis of the evolutionary history of endometrial and ovarian carcinoma in Lynch syndrome. International journal of cancer. 2025;157(11):2294-308.
  • 17. Fraune C, Rosebrock J, Simon R, Hube-Magg C, Makrypidi-Fraune G, Kluth M, et al. High homogeneity of MMR deficiency in ovarian cancer. Gynecologic oncology. 2020;156(3):669-75.
  • 18. Balhara N, Yadav R, Chauhan MB. Role of signaling pathways in endometrial cancer. Molecular biology reports. 2025;52(1):408.
  • 19. Tkacik E, Jang DM, Boxer K, Ha BH, Eck MJ. Characterization and inhibitor sensitivity of ARAF, BRAF, and CRAF kinases. The Journal of biological chemistry. 2025;301(12):110800.
  • 20. Hossain MA. Targeting the RAS upstream and downstream signaling pathway for cancer treatment. European journal of pharmacology. 2024;979:176727.
  • 21. Perrone C, Angioli R, Luvero D, Giannini A, Di Donato V, Cuccu I, et al. Targeting BRAF pathway in low-grade serous ovarian cancer. Journal of gynecologic oncology. 2024;35(4):e104.
  • 22. Hollis RL, Thomson JP, van Baal J, Ilenkovan N, Churchman M, van de Vijver K, et al. Distinct histopathological features are associated with molecular subtypes and outcome in low grade serous ovarian carcinoma. Scientific reports. 2023;13(1):7681.
  • 23. Blagden SP. Targeting MAPK in recurrent, low-grade serous ovarian cancer. Lancet. 2022;399(10324):499-501.
  • 24. Kim JC, Ahn B, Lee YJ, Nam EJ, Kim SW, Kim S, et al. Mismatch repair, p53, and L1 cell adhesion molecule status influence the response to chemotherapy in advanced and recurrent endometrial cancer. BMC cancer. 2024;24(1):1586.
  • 25. Burnett DB, St-Hilaire S, Dodds L, Nelson O, Ravix J, Sowamber R, et al. Mutant p53 disrupts antioxidant defense in fallopian tube epithelium via GSTAs suppression: A pathway to serous tubal carcinogenesis. Free radical biology & medicine. 2026;243:390-7.
  • 26. Smith LE, Padilla JL, Licor A, Steinkamp MP, Lagutina IV, Guo Y, et al. Novel p53 reactivators that are synergistic with olaparib for the treatment of gynecologic cancers with mutant p53. Translational oncology. 2025;61:102522.
  • 27. Montellier E, Manches O, Gaucher J, Freycon C, Hoyos D, Blanchet S, et al. Neoantigenic properties of TP53 variants influence cancer risk in individuals with Li-Fraumeni syndrome. EBioMedicine. 2026;123:106065.
  • 28. Quinn MC, Wojnarowicz PM, Pickett A, Provencher DM, Mes-Masson AM, Davis EC, et al. FKBP10/FKBP65 expression in high-grade ovarian serous carcinoma and its association with patient outcome. International journal of oncology. 2013;42(3):912-20.
  • 29. Kraiczy J, Yu B. Human fallopian tube epithelial organoids with TP53 mutation recapitulate features of serous tubal intraepithelial carcinoma (STIC). Gynecologic oncology. 2025;203:198-208.
  • 30. Park J, Lee D, Kim S, Kim YN, Lee YJ, Park E, et al. Prognostic implications of HER2 in ovarian cancer: Associations with homologous recombination deficiency and folate receptor alpha expression. Gynecologic oncology. 2025;203:151-7.
  • 31. Frezza EG, Nimmagadda GD. Human Epidermal Growth Factor Receptor 2 (HER2/Neu)-Positive Ovarian High-Grade Serous Carcinoma Metastasizing to the Breast: A Case Report. Cureus. 2025;17(9):e92910.
  • 32. Thaker SK, Silverstein J, Konecny GE, Bardia A. Trastuzumab deruxtecan and the evolving role of human epidermal growth factor receptor 2-targeted antibody-drug conjugates in breast and ovarian cancer. Current opinion in obstetrics & gynecology. 2026;38(1):48-56.
  • 33. Allen I, Hassan H, Walburga Y, Huntley C, Loong L, Rahman T, et al. Second Primary Cancer Risks After Breast Cancer in BRCA1 and BRCA2 Pathogenic Variant Carriers. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2025;43(6):651-61.
  • 34. Oswald AJ, Hollis RL, Churchman M, Croy I, Ewing A, Thomson JP, et al. Evaluation of quantitative polymerase chain reaction for detecting BRCA1 or BRCA2 copy number loss in high-grade serous ovarian cancer. Scientific reports. 2026.
  • 35. Jurgiel WA, Panasiuk B, Posmyk R. Hereditary ovarian cancer. Discover oncology. 2026.
  • 36. Apostol AI, Kotsopoulos J, Gronwald J, Kim RH, Karlan BY, Aeilts A, et al. Ovarian cancer after breast cancer in women with a BRCA1 or BRCA2 pathogenic variant. Gynecologic oncology. 2025;201:44-52.
  • 37. Mandilaras V, Garg S, Cabanero M, Tan Q, Pastrello C, Burnier J, et al. TP53 mutations in high grade serous ovarian cancer and impact on clinical outcomes: a comparison of next generation sequencing and bioinformatics analyses. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society. 2019;29(2):346-52.
  • 38. Boerno ST, Grimm C, Lehrach H, Schweiger MR. Next-generation sequencing technologies for DNA methylation analyses in cancer genomics. Epigenomics. 2010;2(2):199-207.
  • 39. Smith AJB, Apple A, Hugo A, Haggerty A, Ko EM. Prior authorization for FDA-approved PARP inhibitors in ovarian cancer. Gynecologic oncology reports. 2024;52:101335.
  • 40. Rodriguez VE, Morrow M, Rajpara R, Chase DM. Endometrial cancer therapy in 2026. Current opinion in obstetrics & gynecology. 2026;38(1):22-33.
  • 41. Crosbie EJ, Kitson SJ, McAlpine JN, Mukhopadhyay A, Powell ME, Singh N. Endometrial cancer. Lancet. 2022;399(10333):1412-28.
  • 42. Huang H, Hartinger S, Geisick RLP, Ho C, Dong F. Preanalytical Histology Review Improves POLE Mutation Detection in Endometrial Carcinomas. The Journal of molecular diagnostics : JMD. 2026;28(1):22-6.
  • 43. Jia Y, Jia H, Mao X, Long X, Yue P, Ye M. A predictive model based on BRCA1/2, POLE, TP53, and MSH6 mutations for immunotherapy response in advanced endometrial cancer. American journal of cancer research. 2025;15(12):5213-30.
  • 44. Wang PH, Yang ST, Chang WH. Mismatch repair (MMR) status detection is the first step for endometrial cancer patients. Taiwanese journal of obstetrics & gynecology. 2025;64(5):770-2.
  • 45. Lim JW, Drost L, Fazelzad R, Li Q, Huszti E, Han K, et al. MLH1 promoter hypermethylated endometrial cancer survival outcomes: A systematic review and meta-analysis. Gynecologic oncology. 2026;204:242-50.
  • 46. Negro S, Celotto F, Schiavi F, Scarpa M, Mammi I, Rossi S, et al. Incidence of non-colorectal/endometrial malignancies in individuals with Lynch syndrome: a retrospective cohort study. EClinicalMedicine. 2025;90:103618.
  • 47. Yang X, Li X, Zhang YL, Zhang SN, Zhang M, Sun C, et al. Targeting undruggable protein KRAS for cancer therapy: novel opportunities and challenges. Future medicinal chemistry. 2025;17(2):143-7.
  • 48. Yang Y, Sang ZY, Ma J, Zhu YP, Wu SF. KRAS, YWHAE, SP1 and MSRA as biomarkers in endometrial cancer. Translational cancer research. 2021;10(3):1295-312.
  • 49. Yu K, Wang Y. The Advance and Correlation of KRAS Mutation With the Fertility-Preservation Treatment of Endometrial Cancer in the Background of Molecular Classification Application. Pathology oncology research : POR. 2021;27:1609906.
  • 50. Da Cruz Paula A, Zhu Y, Brown DN, Issa Bhaloo S, Pareja F, Hoang TJ, et al. Evolution and Co-occurrence of PI3K Pathway Gene Mutations in Endometrial Carcinoma Molecular Subtypes at the Single-Cell Level. Clinical cancer research : an official journal of the American Association for Cancer Research. 2025;31(22):4832-45.
  • 51. Fleming GF, Sill MW, Darcy KM, McMeekin DS, Thigpen JT, Adler LM, et al. Phase II trial of trastuzumab in women with advanced or recurrent, HER2-positive endometrial carcinoma: a Gynecologic Oncology Group study. Gynecologic oncology. 2010;116(1):15-20.
  • 52. Liao J, Chen H, Qi M, Wang J, Wang M. MLLT11-TRIL complex promotes the progression of endometrial cancer through PI3K/AKT/mTOR signaling pathway. Cancer biology & therapy. 2022;23(1):211-24.
  • 53. Keyhanian K, Busca A, Howitt B, Hammer P, Kingsley L, Lo B. Dominant Negative PTEN Alterations in Endometrial Carcinoma Are Associated With Retained Immunohistochemical PTEN Expression. The American journal of surgical pathology. 2025;49(9):923-30.
  • 54. Xing B, Zhang X, Gu X, Xiang L, Wang C, Jin Y. Explore the alterations of downstream molecular pathways caused by ARID1A mutation/knockout in human endometrial cancer cells. Journal of cancer research and clinical oncology. 2023;149(19):17529-41.
  • 55. Cao S, Zhao Y, Zhang L, Zhuang J, Jia P, Han D, et al. Unveiling PIK3CA mutation: a prognostic beacon in endometrial carcinoma and its immune implications. Translational cancer research. 2025;14(10):6469-82.
  • 56. Xu Y, Wang X, Tang L, Shi L, Li M. FABP7 Enhances Endometrial Cancer Cell Migration and Stemness by Activating the Wnt/beta-catenin Pathway. Biochemical genetics. 2025.
  • 57. Lopez-Janeiro A, Brizzi E, Ruz-Caracuel I, Alexandru R, de Andrea C, Berjon A, et al. The Proteomic Landscape of CTNNB1 Mutated Low-Grade Early-Stage Endometrial Carcinomas. Cells. 2025;14(21).
  • 58. Parks SE, Tang S, Unser AC, Bhonsley AL, Chung EM, Jiang P, et al. TGFBR2 coordinates the endometrial response to estrogen, regulating endometrial hyperplasia and fertility. Proceedings of the National Academy of Sciences of the United States of America. 2025;122(49):e2518507122.
  • 59. Liu JL, He JP, Zhu C, Cheng HZ. Endometrial carcinoma may favor partial, but not complete, loss of the TGF-beta signaling pathway. Proceedings of the National Academy of Sciences of the United States of America. 2019;116(19):9164-5.
  • 60. Leon-Castillo A, Britton H, McConechy MK, McAlpine JN, Nout R, Kommoss S, et al. Interpretation of somatic POLE mutations in endometrial carcinoma. The Journal of pathology. 2020;250(3):323-35.
  • 61. Pasciuto MP, Felicioni L, Zampacorta C, Ferro B, Di Marino P, Primavera FC, et al. POLE exonuclease domain mutations in endometrial carcinoma: a case report. Pathologica. 2023;1(1):181-5.
  • 62. Xu J, Wang R, Guan X. Enhancing insights into Global Cancer Statistics 2022: implications for cancer control. Science China Life sciences. 2025;68(1):294-6.
  • 63. Pal A, Kundu R. Human Papillomavirus E6 and E7: The Cervical Cancer Hallmarks and Targets for Therapy. Frontiers in microbiology. 2019;10:3116.
  • 64. Shamseddine AA, Burman B, Lee NY, Zamarin D, Riaz N. Tumor Immunity and Immunotherapy for HPV-Related Cancers. Cancer discovery. 2021;11(8):1896-912.
  • 65. Tota JE, Shing JZ, Roberts JN, Anderson EM, Saah AJ, Harari A, et al. Epidemiological approaches to evaluate clinical unmasking of HPV-associated cervical lesions in the HPV vaccination era. International journal of cancer. 2026;158(4):847-57.
  • 66. Pereira D, Almeida AM, Queiroz JA, Sousa F, Alves N, Valente JFA, et al. Innovative minicircle DNA vector encoding pri-miR-375 silences E6 and E7 oncoproteins in HPV16-positive CaSki cells. Gene. 2026;981:149964.
  • 67. Basukala O, Banks L. The Not-So-Good, the Bad and the Ugly: HPV E5, E6 and E7 Oncoproteins in the Orchestration of Carcinogenesis. Viruses. 2021;13(10).
  • 68. Hidjo M, Mukhedkar D, Masimirembwa C, Lei J, Arroyo Muhr LS. Cervical cancer microbiome analysis: comparing HPV 16 and 18 with other HPV types. Scientific reports. 2024;14(1):22014.
  • 69. Chalertpet K, Pakdeechaidan W, Patel V, Mutirangura A, Yanatatsaneejit P. Human papillomavirus type 16 E7 oncoprotein mediates CCNA1 promoter methylation. Cancer science. 2015;106(10):1333-40.
  • 70. Xu B, Zhang Z, Wang L, Zhang J, Yan X, Du X, et al. Role of SCCA and CYFRA 21-1 in the differential diagnosis of sinonasal benign and malignant diseases. Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery. 2025;53(6):667-73.
  • 71. Singh S, Sarin A, Jain M, Purkayastha A, Shelly D, Bisht N. Role of squamous cell carcinoma antigen (SCC-Ag) in the management of carcinoma cervix in an Indian population: A pilot study. Medical journal, Armed Forces India. 2025;81(4):461-9.
  • 72. Harper DM, Paczos T, Ridder R, Huh WK. p16/ki-67 dual stain triage of individuals positive for HPV to detect cervical precancerous lesions. International journal of cancer. 2025;156(12):2257-64.
  • 73. Damgaard R, Jenkins D, Stoler MH, van de Sandt M, de Koning MNC, Quint WGV, et al. p16(INK4a) and HPV E4 immunohistochemistry for the prediction of regression of cervical intraepithelial neoplasia grade 2-A historical cohort study. International journal of cancer. 2025;157(7):1294-303.
  • 74. Hiller GGR, Wolf B, Forberger M, Freude A, Brambs CE, Droste S, et al. Trop2 expression, p16 expression status, and histologic subtype in carcinoma of the uterine cervix. Pathology oncology research : POR. 2025;31:1612252.
  • 75. Fu X, Duan Z, Lu X, Zhu Y, Ren Y, Zhang W, et al. SND1 Promotes Radioresistance in Cervical Cancer Cells by Targeting the DNA Damage Response. Cancer biotherapy & radiopharmaceuticals. 2024;39(6):425-34.
  • 76. Saha S, Rundle S, Kotsopoulos IC, Begbie J, Howarth R, Pappworth IY, et al. Determining the Potential of DNA Damage Response (DDR) Inhibitors in Cervical Cancer Therapy. Cancers. 2022;14(17).
  • 77. Elayapillai SP, Dogra S, Lausen J, Parker M, Kennedy A, Benbrook DM, et al. ATR inhibition increases reliance on PARP-mediated DNA repair revealing an improved therapeutic strategy for cervical cancer. Gynecologic oncology. 2024;191:182-93.
  • 78. Luo Y, Niu M, Liu Y, Zhang M, Deng Y, Mu D, et al. Oncoproteins E6 and E7 upregulate topoisomerase I to activate the cGAS-PD-L1 pathway in cervical cancer development. Frontiers in pharmacology. 2024;15:1450875.

Jinekolojik Kanserlere Moleküler Yaklaşımlar: Biyobelirteçler ve Hedefli Tedavi Yolları

Year 2026, Volume: 7 Issue: 1 , 86 - 104 , 27.03.2026
https://doi.org/10.46871/eams.1868915
https://izlik.org/JA64SJ72BF

Abstract

Yumurtalık, endometriyum ve servikal maligniteler de dahil olmak üzere jinekolojik kanserler, farklı klinik davranışlar ve karmaşık moleküler özelliklerle karakterize edilen heterojen bir tümör grubudur. Moleküler onkolojideki gelişmeler, jinekolojik karsinogenezin anlaşılmasını önemli ölçüde yeniden şekillendirmiş ve tümör baskılayıcı genlerin düzensizliğinin, DNA hasar onarım yollarının, onkojenik sinyal kaskadlarının ve virüs kaynaklı mekanizmaların hastalık başlangıcını, ilerlemesini ve tedaviye yanıtı kritik olarak etkilediğini ortaya koymuştur. Yumurtalık kanserinde, homolog rekombinasyon onarımındaki değişiklikler, TP53 mutasyonları, MAPK ve PI3K/AKT sinyal yollarının anormal aktivasyonu, moleküler sınıflandırmayı ve hedefe yönelik tedavilerin başarılı bir şekilde uygulanmasını sağlamıştır. Endometriyum kanseri, POLE eksonükleaz mutasyonları, yanlış eşleşme tamir mekanizma eksikliği ve kopya sayısı değişiklikleri ile biyolojik ve klinik olarak farklı alt grupları tanımlayan ve farklı prognostik sonuçlara sahip moleküler sınıflandırmayı temsil etmektedir. Servikal kanser, kalıcı yüksek riskli insan papillomavirüsü enfeksiyonunun hücre döngüsü düzenleyici yollarının bozulmasıyla onkogenezi tetiklediği, virüsle ilişkili maligniteyi temsil eder ve moleküler tanı, önleme stratejileri için biyolojik temeli oluşturur. Bu derleme, CA-125, yanlış eşleşme tamir mekanizması, TP53, HER2, BRCA ile ilişkili DNA onarım mekanizmaları, POLE mutasyonları, WNT/β-katenin sinyallemesi ve HPV ile ilgili moleküler değişiklikler de dahil olmak üzere jinekolojik kanserlerde yer alan temel moleküler biyobelirteçler ve sinyal yolları hakkındaki mevcut bilgileri kapsamlı bir şekilde özetlemektedir. Ayrıca, bu moleküler bilgilerin tanı, prognoz, risk sınıflandırması ve kişiselleştirilmiş tedavi yaklaşımları için klinik etkileri tartışılmaktadır. Sonuç olarak, moleküler profillemenin klinik uygulamaya entegrasyonu, jinekolojik onkolojide hassas tıbba doğru kritik bir adımı temsil etmekte ve biyobelirteç odaklı tanı ve hedefli tedavi stratejileri yoluyla hasta sonuçlarını iyileştirme potansiyeli sunmaktadır.

References

  • 1. Pietras C, Khoo T, Karlin D. Updates in palliative care of patients with gynecologic malignancies in 2026: early integration, resource models, and emerging therapies. Current opinion in obstetrics & gynecology. 2026;38(1):1-5.
  • 2. Rashid H, Ullah A, Ahmad S, Aljahdali SM, Waheed Y, Shaker B, et al. Identification of Novel Genes and Pathways of Ovarian Cancer Using a Comprehensive Bioinformatic Framework. Applied biochemistry and biotechnology. 2024;196(6):3056-75.
  • 3. Caruso G, Weroha SJ, Cliby W. Ovarian Cancer: A Review. Jama. 2025;334(14):1278-91.
  • 4. Anca-Stanciu MB, Manu A, Olinca MV, Coroleuca C, Comandasu DE, Coroleuca CA, et al. Comprehensive Review of Endometrial Cancer: New Molecular and FIGO Classification and Recent Treatment Changes. Journal of clinical medicine. 2025;14(4).
  • 5. Sahasrabuddhe VV. Cervical Cancer: Precursors and Prevention. Hematology/oncology clinics of North America. 2024;38(4):771-81.
  • 6. Ullah A, Chen Y, Shen Y, Shen B. Chemotherapy as a double-edged sword: Modulation of tumor-associated cytokine and chemokine responses in ovarian cancer. International journal of cancer. 2026;158(5):1141-55.
  • 7. Shin KH, Kim HH, Kwon BS, Suh DS, Joo JK, Kim KH. Clinical Usefulness of Cancer Antigen (CA) 125, Human Epididymis 4, and CA72-4 Levels and Risk of Ovarian Malignancy Algorithm Values for Diagnosing Ovarian Tumors in Korean Patients With and Without Endometriosis. Annals of laboratory medicine. 2020;40(1):40-7.
  • 8. Teh BH, Yong SL, Sim WW, Lau KB, Suharjono HN. Evaluation in the predictive value of serum human epididymal protein 4 (HE4), cancer antigen 125 (CA 125) and a combination of both in detecting ovarian malignancy. Hormone molecular biology and clinical investigation. 2018;35(1).
  • 9. Chen F, Shen J, Wang J, Cai P, Huang Y. Clinical analysis of four serum tumor markers in 458 patients with ovarian tumors: diagnostic value of the combined use of HE4, CA125, CA19-9, and CEA in ovarian tumors. Cancer management and research. 2018;10:1313-8.
  • 10. Ghose A, McCann L, Makker S, Mukherjee U, Gullapalli SVN, Erekkath J, et al. Diagnostic biomarkers in ovarian cancer: advances beyond CA125 and HE4. Therapeutic advances in medical oncology. 2024;16:17588359241233225.
  • 11. Sameer AS, Nissar S, Fatima K. Mismatch repair pathway: molecules, functions, and role in colorectal carcinogenesis. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation. 2014;23(4):246-57.
  • 12. Carethers JM, Stoffel EM. Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancer. World journal of gastroenterology. 2015;21(31):9253-61.
  • 13. Eroglu S, Birsenogul I, Bowen AP, Doyle JF, Pupkin SE, Villar J, et al. Lynch Syndrome in Focus: A Multidisciplinary Review of Cancer Risk, Clinical Management, and Special Populations. Cancers. 2025;17(24).
  • 14. Akbari MR, Zhang S, Cragun D, Lee JH, Coppola D, McLaughlin J, et al. Correlation between germline mutations in MMR genes and microsatellite instability in ovarian cancer specimens. Familial cancer. 2017;16(3):351-5.
  • 15. Kruckel A, Gocke J, Horner M, Keller K, Muller C, Bruckner L, et al. Genetic tumor syndromes in female cancer: insights into inherited cancer predisposition and clinical implications. Archives of gynecology and obstetrics. 2026;313(1):38.
  • 16. Kauppinen AK, Olkinuora AP, Mecklin JP, Peltomaki PT. Molecular analysis of the evolutionary history of endometrial and ovarian carcinoma in Lynch syndrome. International journal of cancer. 2025;157(11):2294-308.
  • 17. Fraune C, Rosebrock J, Simon R, Hube-Magg C, Makrypidi-Fraune G, Kluth M, et al. High homogeneity of MMR deficiency in ovarian cancer. Gynecologic oncology. 2020;156(3):669-75.
  • 18. Balhara N, Yadav R, Chauhan MB. Role of signaling pathways in endometrial cancer. Molecular biology reports. 2025;52(1):408.
  • 19. Tkacik E, Jang DM, Boxer K, Ha BH, Eck MJ. Characterization and inhibitor sensitivity of ARAF, BRAF, and CRAF kinases. The Journal of biological chemistry. 2025;301(12):110800.
  • 20. Hossain MA. Targeting the RAS upstream and downstream signaling pathway for cancer treatment. European journal of pharmacology. 2024;979:176727.
  • 21. Perrone C, Angioli R, Luvero D, Giannini A, Di Donato V, Cuccu I, et al. Targeting BRAF pathway in low-grade serous ovarian cancer. Journal of gynecologic oncology. 2024;35(4):e104.
  • 22. Hollis RL, Thomson JP, van Baal J, Ilenkovan N, Churchman M, van de Vijver K, et al. Distinct histopathological features are associated with molecular subtypes and outcome in low grade serous ovarian carcinoma. Scientific reports. 2023;13(1):7681.
  • 23. Blagden SP. Targeting MAPK in recurrent, low-grade serous ovarian cancer. Lancet. 2022;399(10324):499-501.
  • 24. Kim JC, Ahn B, Lee YJ, Nam EJ, Kim SW, Kim S, et al. Mismatch repair, p53, and L1 cell adhesion molecule status influence the response to chemotherapy in advanced and recurrent endometrial cancer. BMC cancer. 2024;24(1):1586.
  • 25. Burnett DB, St-Hilaire S, Dodds L, Nelson O, Ravix J, Sowamber R, et al. Mutant p53 disrupts antioxidant defense in fallopian tube epithelium via GSTAs suppression: A pathway to serous tubal carcinogenesis. Free radical biology & medicine. 2026;243:390-7.
  • 26. Smith LE, Padilla JL, Licor A, Steinkamp MP, Lagutina IV, Guo Y, et al. Novel p53 reactivators that are synergistic with olaparib for the treatment of gynecologic cancers with mutant p53. Translational oncology. 2025;61:102522.
  • 27. Montellier E, Manches O, Gaucher J, Freycon C, Hoyos D, Blanchet S, et al. Neoantigenic properties of TP53 variants influence cancer risk in individuals with Li-Fraumeni syndrome. EBioMedicine. 2026;123:106065.
  • 28. Quinn MC, Wojnarowicz PM, Pickett A, Provencher DM, Mes-Masson AM, Davis EC, et al. FKBP10/FKBP65 expression in high-grade ovarian serous carcinoma and its association with patient outcome. International journal of oncology. 2013;42(3):912-20.
  • 29. Kraiczy J, Yu B. Human fallopian tube epithelial organoids with TP53 mutation recapitulate features of serous tubal intraepithelial carcinoma (STIC). Gynecologic oncology. 2025;203:198-208.
  • 30. Park J, Lee D, Kim S, Kim YN, Lee YJ, Park E, et al. Prognostic implications of HER2 in ovarian cancer: Associations with homologous recombination deficiency and folate receptor alpha expression. Gynecologic oncology. 2025;203:151-7.
  • 31. Frezza EG, Nimmagadda GD. Human Epidermal Growth Factor Receptor 2 (HER2/Neu)-Positive Ovarian High-Grade Serous Carcinoma Metastasizing to the Breast: A Case Report. Cureus. 2025;17(9):e92910.
  • 32. Thaker SK, Silverstein J, Konecny GE, Bardia A. Trastuzumab deruxtecan and the evolving role of human epidermal growth factor receptor 2-targeted antibody-drug conjugates in breast and ovarian cancer. Current opinion in obstetrics & gynecology. 2026;38(1):48-56.
  • 33. Allen I, Hassan H, Walburga Y, Huntley C, Loong L, Rahman T, et al. Second Primary Cancer Risks After Breast Cancer in BRCA1 and BRCA2 Pathogenic Variant Carriers. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2025;43(6):651-61.
  • 34. Oswald AJ, Hollis RL, Churchman M, Croy I, Ewing A, Thomson JP, et al. Evaluation of quantitative polymerase chain reaction for detecting BRCA1 or BRCA2 copy number loss in high-grade serous ovarian cancer. Scientific reports. 2026.
  • 35. Jurgiel WA, Panasiuk B, Posmyk R. Hereditary ovarian cancer. Discover oncology. 2026.
  • 36. Apostol AI, Kotsopoulos J, Gronwald J, Kim RH, Karlan BY, Aeilts A, et al. Ovarian cancer after breast cancer in women with a BRCA1 or BRCA2 pathogenic variant. Gynecologic oncology. 2025;201:44-52.
  • 37. Mandilaras V, Garg S, Cabanero M, Tan Q, Pastrello C, Burnier J, et al. TP53 mutations in high grade serous ovarian cancer and impact on clinical outcomes: a comparison of next generation sequencing and bioinformatics analyses. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society. 2019;29(2):346-52.
  • 38. Boerno ST, Grimm C, Lehrach H, Schweiger MR. Next-generation sequencing technologies for DNA methylation analyses in cancer genomics. Epigenomics. 2010;2(2):199-207.
  • 39. Smith AJB, Apple A, Hugo A, Haggerty A, Ko EM. Prior authorization for FDA-approved PARP inhibitors in ovarian cancer. Gynecologic oncology reports. 2024;52:101335.
  • 40. Rodriguez VE, Morrow M, Rajpara R, Chase DM. Endometrial cancer therapy in 2026. Current opinion in obstetrics & gynecology. 2026;38(1):22-33.
  • 41. Crosbie EJ, Kitson SJ, McAlpine JN, Mukhopadhyay A, Powell ME, Singh N. Endometrial cancer. Lancet. 2022;399(10333):1412-28.
  • 42. Huang H, Hartinger S, Geisick RLP, Ho C, Dong F. Preanalytical Histology Review Improves POLE Mutation Detection in Endometrial Carcinomas. The Journal of molecular diagnostics : JMD. 2026;28(1):22-6.
  • 43. Jia Y, Jia H, Mao X, Long X, Yue P, Ye M. A predictive model based on BRCA1/2, POLE, TP53, and MSH6 mutations for immunotherapy response in advanced endometrial cancer. American journal of cancer research. 2025;15(12):5213-30.
  • 44. Wang PH, Yang ST, Chang WH. Mismatch repair (MMR) status detection is the first step for endometrial cancer patients. Taiwanese journal of obstetrics & gynecology. 2025;64(5):770-2.
  • 45. Lim JW, Drost L, Fazelzad R, Li Q, Huszti E, Han K, et al. MLH1 promoter hypermethylated endometrial cancer survival outcomes: A systematic review and meta-analysis. Gynecologic oncology. 2026;204:242-50.
  • 46. Negro S, Celotto F, Schiavi F, Scarpa M, Mammi I, Rossi S, et al. Incidence of non-colorectal/endometrial malignancies in individuals with Lynch syndrome: a retrospective cohort study. EClinicalMedicine. 2025;90:103618.
  • 47. Yang X, Li X, Zhang YL, Zhang SN, Zhang M, Sun C, et al. Targeting undruggable protein KRAS for cancer therapy: novel opportunities and challenges. Future medicinal chemistry. 2025;17(2):143-7.
  • 48. Yang Y, Sang ZY, Ma J, Zhu YP, Wu SF. KRAS, YWHAE, SP1 and MSRA as biomarkers in endometrial cancer. Translational cancer research. 2021;10(3):1295-312.
  • 49. Yu K, Wang Y. The Advance and Correlation of KRAS Mutation With the Fertility-Preservation Treatment of Endometrial Cancer in the Background of Molecular Classification Application. Pathology oncology research : POR. 2021;27:1609906.
  • 50. Da Cruz Paula A, Zhu Y, Brown DN, Issa Bhaloo S, Pareja F, Hoang TJ, et al. Evolution and Co-occurrence of PI3K Pathway Gene Mutations in Endometrial Carcinoma Molecular Subtypes at the Single-Cell Level. Clinical cancer research : an official journal of the American Association for Cancer Research. 2025;31(22):4832-45.
  • 51. Fleming GF, Sill MW, Darcy KM, McMeekin DS, Thigpen JT, Adler LM, et al. Phase II trial of trastuzumab in women with advanced or recurrent, HER2-positive endometrial carcinoma: a Gynecologic Oncology Group study. Gynecologic oncology. 2010;116(1):15-20.
  • 52. Liao J, Chen H, Qi M, Wang J, Wang M. MLLT11-TRIL complex promotes the progression of endometrial cancer through PI3K/AKT/mTOR signaling pathway. Cancer biology & therapy. 2022;23(1):211-24.
  • 53. Keyhanian K, Busca A, Howitt B, Hammer P, Kingsley L, Lo B. Dominant Negative PTEN Alterations in Endometrial Carcinoma Are Associated With Retained Immunohistochemical PTEN Expression. The American journal of surgical pathology. 2025;49(9):923-30.
  • 54. Xing B, Zhang X, Gu X, Xiang L, Wang C, Jin Y. Explore the alterations of downstream molecular pathways caused by ARID1A mutation/knockout in human endometrial cancer cells. Journal of cancer research and clinical oncology. 2023;149(19):17529-41.
  • 55. Cao S, Zhao Y, Zhang L, Zhuang J, Jia P, Han D, et al. Unveiling PIK3CA mutation: a prognostic beacon in endometrial carcinoma and its immune implications. Translational cancer research. 2025;14(10):6469-82.
  • 56. Xu Y, Wang X, Tang L, Shi L, Li M. FABP7 Enhances Endometrial Cancer Cell Migration and Stemness by Activating the Wnt/beta-catenin Pathway. Biochemical genetics. 2025.
  • 57. Lopez-Janeiro A, Brizzi E, Ruz-Caracuel I, Alexandru R, de Andrea C, Berjon A, et al. The Proteomic Landscape of CTNNB1 Mutated Low-Grade Early-Stage Endometrial Carcinomas. Cells. 2025;14(21).
  • 58. Parks SE, Tang S, Unser AC, Bhonsley AL, Chung EM, Jiang P, et al. TGFBR2 coordinates the endometrial response to estrogen, regulating endometrial hyperplasia and fertility. Proceedings of the National Academy of Sciences of the United States of America. 2025;122(49):e2518507122.
  • 59. Liu JL, He JP, Zhu C, Cheng HZ. Endometrial carcinoma may favor partial, but not complete, loss of the TGF-beta signaling pathway. Proceedings of the National Academy of Sciences of the United States of America. 2019;116(19):9164-5.
  • 60. Leon-Castillo A, Britton H, McConechy MK, McAlpine JN, Nout R, Kommoss S, et al. Interpretation of somatic POLE mutations in endometrial carcinoma. The Journal of pathology. 2020;250(3):323-35.
  • 61. Pasciuto MP, Felicioni L, Zampacorta C, Ferro B, Di Marino P, Primavera FC, et al. POLE exonuclease domain mutations in endometrial carcinoma: a case report. Pathologica. 2023;1(1):181-5.
  • 62. Xu J, Wang R, Guan X. Enhancing insights into Global Cancer Statistics 2022: implications for cancer control. Science China Life sciences. 2025;68(1):294-6.
  • 63. Pal A, Kundu R. Human Papillomavirus E6 and E7: The Cervical Cancer Hallmarks and Targets for Therapy. Frontiers in microbiology. 2019;10:3116.
  • 64. Shamseddine AA, Burman B, Lee NY, Zamarin D, Riaz N. Tumor Immunity and Immunotherapy for HPV-Related Cancers. Cancer discovery. 2021;11(8):1896-912.
  • 65. Tota JE, Shing JZ, Roberts JN, Anderson EM, Saah AJ, Harari A, et al. Epidemiological approaches to evaluate clinical unmasking of HPV-associated cervical lesions in the HPV vaccination era. International journal of cancer. 2026;158(4):847-57.
  • 66. Pereira D, Almeida AM, Queiroz JA, Sousa F, Alves N, Valente JFA, et al. Innovative minicircle DNA vector encoding pri-miR-375 silences E6 and E7 oncoproteins in HPV16-positive CaSki cells. Gene. 2026;981:149964.
  • 67. Basukala O, Banks L. The Not-So-Good, the Bad and the Ugly: HPV E5, E6 and E7 Oncoproteins in the Orchestration of Carcinogenesis. Viruses. 2021;13(10).
  • 68. Hidjo M, Mukhedkar D, Masimirembwa C, Lei J, Arroyo Muhr LS. Cervical cancer microbiome analysis: comparing HPV 16 and 18 with other HPV types. Scientific reports. 2024;14(1):22014.
  • 69. Chalertpet K, Pakdeechaidan W, Patel V, Mutirangura A, Yanatatsaneejit P. Human papillomavirus type 16 E7 oncoprotein mediates CCNA1 promoter methylation. Cancer science. 2015;106(10):1333-40.
  • 70. Xu B, Zhang Z, Wang L, Zhang J, Yan X, Du X, et al. Role of SCCA and CYFRA 21-1 in the differential diagnosis of sinonasal benign and malignant diseases. Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery. 2025;53(6):667-73.
  • 71. Singh S, Sarin A, Jain M, Purkayastha A, Shelly D, Bisht N. Role of squamous cell carcinoma antigen (SCC-Ag) in the management of carcinoma cervix in an Indian population: A pilot study. Medical journal, Armed Forces India. 2025;81(4):461-9.
  • 72. Harper DM, Paczos T, Ridder R, Huh WK. p16/ki-67 dual stain triage of individuals positive for HPV to detect cervical precancerous lesions. International journal of cancer. 2025;156(12):2257-64.
  • 73. Damgaard R, Jenkins D, Stoler MH, van de Sandt M, de Koning MNC, Quint WGV, et al. p16(INK4a) and HPV E4 immunohistochemistry for the prediction of regression of cervical intraepithelial neoplasia grade 2-A historical cohort study. International journal of cancer. 2025;157(7):1294-303.
  • 74. Hiller GGR, Wolf B, Forberger M, Freude A, Brambs CE, Droste S, et al. Trop2 expression, p16 expression status, and histologic subtype in carcinoma of the uterine cervix. Pathology oncology research : POR. 2025;31:1612252.
  • 75. Fu X, Duan Z, Lu X, Zhu Y, Ren Y, Zhang W, et al. SND1 Promotes Radioresistance in Cervical Cancer Cells by Targeting the DNA Damage Response. Cancer biotherapy & radiopharmaceuticals. 2024;39(6):425-34.
  • 76. Saha S, Rundle S, Kotsopoulos IC, Begbie J, Howarth R, Pappworth IY, et al. Determining the Potential of DNA Damage Response (DDR) Inhibitors in Cervical Cancer Therapy. Cancers. 2022;14(17).
  • 77. Elayapillai SP, Dogra S, Lausen J, Parker M, Kennedy A, Benbrook DM, et al. ATR inhibition increases reliance on PARP-mediated DNA repair revealing an improved therapeutic strategy for cervical cancer. Gynecologic oncology. 2024;191:182-93.
  • 78. Luo Y, Niu M, Liu Y, Zhang M, Deng Y, Mu D, et al. Oncoproteins E6 and E7 upregulate topoisomerase I to activate the cGAS-PD-L1 pathway in cervical cancer development. Frontiers in pharmacology. 2024;15:1450875.
There are 78 citations in total.

Details

Primary Language English
Subjects Molecular Targets
Journal Section Review
Authors

Sevide Şencan 0000-0002-4312-1043

Submission Date January 21, 2026
Acceptance Date March 9, 2026
Early Pub Date March 27, 2026
Publication Date March 27, 2026
DOI https://doi.org/10.46871/eams.1868915
IZ https://izlik.org/JA64SJ72BF
Published in Issue Year 2026 Volume: 7 Issue: 1

Cite

Vancouver 1.Sevide Şencan. Molecular Approaches to Gynecological Cancers: Biomarkers and Targeted Therapeutic Pathways. Exp Appl Med Sci. 2026 Mar. 1;7(1):86-104. doi:10.46871/eams.1868915

Aim & Scope

Deneysel ve Uygulamalı Tıp Bilimleri, tıp bilimlerinin her alanından özgün ve yaşam kalitesini artıracak çarpıcı araştırma sonuçlarının yer aldığı güncel ve kolay erişilebilir bir akademik yayın olmayı hedeflemektedir.

Experimental and Applied Medical Science, Gaziantep İslam Bilim ve Teknoloji Üniversitesi Tıp Fakültesi bünyesinde yılda dört kez İngilizce olarak yayımlanan, açık erişimli, uluslararası çift-kör hakemli akademik bir tıp dergisidir. Dergi, hastalıkların patogenezi ile ilgili deneysel hayvan çalışmaları, farmakolojik, klinik, epidemiyolojik ve deontolojik çalışmalar, ayrıca halk sağlığını geliştirme, sağlık hizmetleri veya sağlık sigortası alanlarındaki çalışmaları içeren, yurt içinden veya yurt dışından sunulmuş araştırma makalesi, derleme, editöre mektup, kısa bildirim, özet bildirim vb. şeklinde yayınlanmak üzere yazıları kabul etmektedir.

Değerlendirme veya yayın sırasında yazarlardan herhangi bir ücret talep edilmez. Dergi 3 ayda bir (Mart, Temmuz, Eylül ve Aralık) olmak üzere yılda 4 sayı yayınlanmaktadır. Derginin yazım dili İngilizcedir. Makalenin sadece özet kısmı Türkçe olarak da gönderilmelidir.

Deneysel ve Uygulamalı Tıp Bilimleri dergisi; özgün araştırma makaleleri, derlemeler, olgu sunumları ve editöre mektuplar kabul etmektedir. Bir makalenin gönderilmesi, daha önce yayımlanmadığını ve başka bir yerde yayımlanmak üzere değerlendirilmediğini ima eder. Gönderilen makalelerin yayımlanıp yayımlanmayacağına dair karar, makalenin önemine ve özgünlüğüne ilişkin Editör Kurulu'nun görüşüne dayanır.
Dergiye gönderilen makalelerin tüm yazarları (sorumlu yazar ve diğer yazarlar), bireysel bir ORCID (Open Researcher and Contributor ID) numarası almalı (http://orcid.org) ve bu numarayı makalenin başlık sayfasında belirtmelidir. Sorumlu yazar, tüm yazarları DergiPark sistemine eklemelidir.
Makaleler
Makaleler, elektronik olarak "Microsoft Word" formatında, "Times New Roman" yazı tipi, 12 punto ve çift aralıklı olarak yazılmalıdır. Makaleler İngilizce yazılmalı; özetler ise hem Türkçe hem de İngilizce hazırlanmalıdır. Sayfanın her iki yanında 2.5 cm boşluk bırakılmalı ve metin iki yana yaslı olmalıdır. Kelimeler satır sonlarında kesilmemelidir. Sayfalar ardışık olarak numaralandırılmalıdır.
Makale, "Başlık sayfası", "Türkçe Özet", "İngilizce Özet", "Metin", "Kaynaklar", "Tablolar" ve "Şekiller" gibi bölümleri içermeli ve her bölüm ayrı bir sayfadan başlamalıdır.
Özgün araştırma makaleleri için gerekli etik kurul izinleri alınmalı ve etik kurul numarası ile tarihi makalede belirtilmelidir. Çalışmanın intihal raporu yüklenmeli ve intihal oranı %30'u geçmemelidir.
Makalenizi sisteme yüklerken dosya adını sorumlu yazarın adı ve soyadı olarak belirleyiniz.
Başlık Sayfası
Başlık sayfasında Türkçe ve İngilizce başlıklar ayrı ayrı verilmelidir. Başlıkta kısaltmalar kullanılmamalıdır.
• Tüm yazarlar için ORCID numaraları, özet ve metnin kelime sayıları (özet, tablolar ve kaynaklar hariç) belirtilmelidir.
• Yazarların tam isimleri, soyadları, akademik unvanları, görev yaptıkları kurum, çalışmanın yapıldığı klinik/bölüm/enstitü/hastane/üniversitenin tam adı ve adresi ile e-posta adresleri belirtilmelidir.
• Sorumlu yazarın iletişim bilgileri (güncel adres, e-posta adresi ve GSM telefon numarası) eklenmelidir.
• Çalışma daha önce bir bilimsel toplantıda sunulmuşsa ya da özeti yayımlanmışsa bu durum belirtilmelidir.
• Tüm yazarların olası çıkar çatışmaları ve finansal destek bilgileri, konu ile doğrudan ilişkili olup olmadığına bakılmaksızın, bireysel olarak açıklanmalıdır.
Özet
Türkçe ve İngilizce özetler ayrı hazırlanmalı ve her biri 250 kelimeyi geçmemelidir. Türkçe özet şu başlıkları içermelidir: Amaç, Yöntem, Bulgular, Sonuç, Anahtar Kelimeler. İngilizce özet ise şu başlıklardan oluşmalıdır: Purpose, Methods, Results, Conclusion, Keywords.
Metin
Metin; "Giriş", "Yöntem", "Bulgular", "Tartışma" ve "Sonuç" bölümlerinden oluşmalıdır. Metin sonunda "Çıkar Çatışması" ve "Teşekkür" bölümleri eklenmelidir.
• Fazla kısaltma kullanılmamalıdır.
• Tablolar, grafikler ve şekiller metin sonunda ayrı birer sayfada yer almalıdır.
Kaynaklar, Vancouver formatında düzenlenmeli ve metinde geçtiği sıraya göre numaralandırılmalıdır.

Makaleler yalnızca orijinal olmaları, başka bir dergide eşzamanlı olarak değerlendirilmemeleri veya daha önce yayımlanmamış olmaları koşuluyla yayımlanmak üzere değerlendirilir. Telif hakkı ile korunan herhangi bir materyalden alınan doğrudan alıntılar, tablolar veya görseller için telif hakkı sahiplerinden yazılı izin alınmalıdır. Tüm makaleler editörler ve hakemler tarafından incelenir. Yayınlanmaya uygunluk, sunulan materyalin önemine ve özgünlüğüne dayanır. Yayınlanması uygun görülen makaleler, sunulan veriler değiştirilmeden, açık ve anlaşılır bir şekilde sunulması için editöryal revizyona tabi tutulabilir.
Experimental and Applied Medical Science, aşağıdaki web adresinde yer alan “Helsinki Bildirgesi” ilkelerine sıkı sıkıya bağlıdır:
Helsinki Bildirgesi
Editör Kurulu, insanlarla yapılan tüm çalışmaların bu ilkelere uygun olması gerektiğini beyan eder.
İnsan katılımcılarla yapılan çalışmaların verilerini içeren makalelerde, Yöntem ve Materyal bölümünde çalışmanın kurum etik inceleme kurulu tarafından onaylandığını ve her katılımcıdan “bilgilendirilmiş onam” alındığını belirten açıklamalar yer almalıdır. Ayrıca, laboratuvar hayvanlarıyla yapılan deneyleri bildiren makalelerde, hayvanların “Laboratuvar Hayvanlarının Bakımı ve Kullanımı Kılavuzu” ile uyumlu bir şekilde insan bakımına tabi tutulduğunu ve kurum etik kurul onayının alındığını doğrulayan açıklamalar Yöntem ve Materyal bölümünde yer almalıdır.
Laboratuvar Hayvanları Kılavuzu
Eğer çalışmayı destekleyen ticari bir ilişki veya mali destek sağlayan bir kurum varsa, yazarlar bu ürün, ilaç veya şirket ile ticari bir ilişkileri olmadığını veya varsa ne tür bir ilişkiye (danışmanlık ya da başka bir anlaşma) sahip olduklarını beyan etmelidir.
Dergi için işlem ve yayın ücretsizdir. Değerlendirme ve yayın sürecinin hiçbir aşamasında yazarlardan ücret talep edilmez. Tüm makaleler, yalnızca çevrimiçi başvuru sistemi aracılığıyla gönderilmelidir:
https://dergipark.org.tr/tr/pub/eams
Derginin yönergeleri, teknik bilgileri ve gerekli formlar da derginin web sayfasında mevcuttur.
Derginin tüm masrafları Gaziantep İslam Bilim ve Teknoloji Üniversitesi Tıp Fakültesi tarafından karşılanmaktadır. Potansiyel reklam verenler derginin Editör Ofisi ile iletişime geçmelidir. Reklam görselleri yalnızca Baş Editör'ün onayı ile yayımlanır.
Makalelerde ifade edilen görüş ve öneriler, Gaziantep İslam Bilim ve Teknoloji Üniversitesi Tıp Fakültesi, editörler, editör kurulu ve/veya yayıncıların görüşlerini yansıtmaz; bu içeriklerin sorumluluğu tamamen yazar(lar)a aittir.
Araştırma çalışmalarını içeren tüm makaleler, biyostatistik açısından değerlendirilmelidir ve uygun çalışma tasarımı, analiz ve sonuçlarla birlikte sunulmalıdır. Makalelerde p değerleri net bir şekilde belirtilmelidir. Araştırma makaleleri dışındaki (derleme, olgu sunumu, editöre mektup vb.) yazılar da özgün, güncel ve kaynaklarıyla birlikte açık, anlaşılır ve tatmin edici olmalıdır.
Derginin yayın dili İngilizce’dir. Ancak makalenin özet kısmı hem Türkçe hem de İngilizce olarak yüklenmelidir. Makaleler dergiye gönderilmeden önce bir dil uzmanı tarafından değerlendirilmelidir.
Telif Hakkı ve Yayımlama Hakları:
5846 sayılı ve 13.12.1951 tarihli Fikir ve Sanat Eserleri Kanunu’na göre (aşağıdaki bağlantıda yer alan) yayımlanması kabul edilen makalelerin tüm yayım hakları dergiyi yayımlayan kuruma aittir. Ancak makalelerde ifade edilen düşünceler ve öneriler tamamen yazarların sorumluluğundadır.
Fikir ve Sanat Eserleri Kanunu

Experimental and Applied Medical Science dergisinde makale değerlendirme ve yayın süreci tamamen ücretsizdir.

Editör

Cell Development, Proliferation and Death, Histology and Embryology, Reproduction

Editör Yardımcıları

Molecular Genetics

2008 yılında Hacettepe Üniversitesi Tıp (İng). Fakültesi'nden mezun oldu. 2018 yılında Gaziantep Üniversitesi Tıp Fakültesi Fizyoloji Anabilim Dalı'nda Tıbbi Fizyoloji alanında doktoramı tamamladı. 2019 yılından bu yana Gaziantep İslam Bilim ve Teknoloji Üniversitesi Tıp Fakültesi Fizyoloji Anabilim Dalı'nda öğretim üyesi olarak görev yapmaktadır. Başlıca çalışma alanları, Alzheimer Hastalığı, egzersiz ve elektrokardiyografidir.

Medical Physiology, Family Medicine

Yayın Kurulu

Medical Microbiology, Health Sciences
Histology and Embryology
Medical Microbiology, Veterinary Microbiology
Biological Sciences, Genomics and Transcriptomics, Cancer Biology, Epigenetics, Molecular Genetics
Nutrition and Dietetics, Public Health Nutrition, Nutritional Epidemiology, Public Health
Pharmaceutical Toxicology, Basic Pharmacology, Medical Pharmacology, Toxicology, Health Sciences
Medical Biochemistry and Metabolomics

Alan Editörleri

Health Sciences
Public Health, Preventative Health Care, Health Promotion, Social Determinants of Health, Community Child Health, Health Literacy
Medical Biochemistry and Metabolomics
Molecular Genetics, Medical Genetics (Excl. Cancer Genetics), Bioengineering, Animal Cell Culture and Tissue Engineering
Developmental Genetics, Neurogenetics, Cytogenetic, Molecular Genetics
Physiotherapy, Rehabilitation
Statistics, Biostatistics, Statistical Analysis, Applied Statistics
Cell Development, Proliferation and Death, Histology and Embryology, Reproduction
Cell Development, Proliferation and Death, Proteomics and Intermolecular Interactions, Animal Cell and Molecular Biology, Bioengineering (Other)
Physiotherapy, Rehabilitation

Daniele Saverino is an Associate Professor of Human Anatomy at the University of Genoa. He holds the following university degrees: Degree in Medicine, Degree in Biological Sciences, Specialization in Allergology and Clinical Immunology, and Master's in Microbiological Sciences.

He is currently a member of the Board of the Department of Experimental Medicine, a member of the Scientific Council University Service Center, University Service Center of Simulation and Advanced Training – SIMAV of the University of Genoa (Italy); he is also a medical director at the IRCCS San Martino Polyclinic in Genoa.

He is the holder of the Human Anatomy courses for the degree courses in Medicine and Surgery, Physiotherapy, Motor Sciences at the University of Genoa and the Neuroanatomy Course, Degree in Medicine at the Vita e Salute University of Milan (Italy) He was a Research fellow, Brown University, The Miriam Hospital, Providence, Rhode Island, USA.

His research interests and activity are mostly closely connected to diagnostic activity: study and experimentation of new analytical technologies, diagnostic experimentation of new autoantibody markers in various areas of pathology, development, experimentation and validation of specific diagnostic algorithms, participation, for the diagnostic part of competence, in clinical trials and studies.

He is also involved in pathophysiological studies concerning alterations of immunoregulatory and effector mechanisms in systemic and organ-specific autoimmune diseases, with particular reference to the role and regulation of "immune checkpoint" molecules.

Autoimmunity
Cancer Biology, Immunogenetics, Transplantation Immunology, Tumour Immunology, Cancer Genetics, Cancer Cell Biology, Medical Biochemistry and Metabolomics
Obstetrics and Gynaecology
Cancer Biology, Molecular Genetics, Mechanobiology
Cancer Biology, Molecular Genetics, Cancer Genetics, Cancer Cell Biology

Dr. Roghaiyeh Safari, 15 yılı aşkın deneyimiyle moleküler tıp alanında uzmanlaşmış bir bilim insanıdır. Imperial College London, Sahlgrenska Kanser Merkezi (İsveç), Liège Üniversitesi (Belçika) ve İzmir Biyotıp ve Genom Merkezi (IBG) gibi prestijli kurumlarda yürüttüğü araştırmalarla moleküler biyoloji ve genetik alanında geniş bir uzmanlık edinmiştir.

RS & RS Scientific’in Kurucu Ortağı ve Bilimsel Direktörü (CSO) olarak, iş birliğine dayalı bir araştırma ortamı oluşturmakta ve bilimsel keşifleri kanser tedavisine yönelik pratik çözümlere dönüştürme konusunda endüstri deneyimini kullanmaktadır.

Moleküler araştırmalar konusundaki uzmanlığının yanı sıra, liderlik koçluğu yapmaktadır ve klinik geçmişi sayesinde hasta odaklı bir yaklaşım benimsemektedir.

Cancer Biology, Molecular Genetics
Cellular Interactions, Mechanobiology

Avrupa Board sertifikalı göz hastalıkları uzmanı ve Gaziantep İslam Bilim ve Teknoloji Üniversitesi’nde öğretim üyesidir. Oküloplastik cerrahi ve ön segment alanında uzmanlaşmış olup 2.000’den fazla katarakt, 600’den fazla oküloplastik ve 200’den fazla şaşılık ameliyatı deneyimine sahiptir. Ulusal ve uluslararası dergilerde çok sayıda yayını, kitap bölümleri ve kongre sunumları bulunan Yılmaz, akademik hareketlilik programları ve bilimsel işbirlikleriyle mesleki gelişimini sürdürmekte ve göz hastalıkları eğitimine katkı sağlamaktadır.  

War Surgery, Ophthalmology and Optometry, Ophthalmology

Teknik Editör

Biological Sciences, Mycology

Mizanpaj Editörleri

Histology and Embryology
Medical Physiology, Medical Physiology (Other), Health Sciences

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