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İnsan Kronik Myeloid Lösemi Hücreleri Üzerine Florlu Shiff Bazı Ligandları ile Bunların Bakır ve Paladyum Komplekslerinin Antikanser Aktiviteleri

Year 2026, Volume: 10 Issue: 1 , 79 - 87 , 29.04.2026
https://doi.org/10.46332/aemj.1637016
https://izlik.org/JA97AN98MX

Abstract

Amaç: Kanser tedavisinde kemoterapatiklere bağlı yan etkilerin ortaya çıkması, ilaç direnci gelişimi en önemli sorunların başında gelmektedir. Bu güçlüklerin üstesinden gelebilmek için yeni antikanser ajanları araştırmalarına olan ihtiyaç artmaktadır. Son yıllarda Schiff bazlarının antikanser aktiviteye sahip olduğuna dair veriler dikkat çekmektedir. Bu bileşiklerin kanser hücrelerinde apoptozu
indükleyerek hücre ölümüne yol açtığı ve DNA ve RNA sentezini durdurarak hücre çoğalmasını engellediği bildirilmektedir.Çalışmada, florlu Schiff bazları ile bunların bakır ve paladyum komplekslerinin insan kronik myeloid lösemi hücreleri üzerindeki sitotoksik etkileri araştırılmıştır.

Araçlar ve Yöntem: K562 lösemi hücrelerinde florlu Schiff bazlarından o-florofenil-3,5-di-tert-butilsalisilaldimin [o-FPh-3,5-DTBS] ve p-florofenil-3,5-di-tert-butilsalisilaldimin [o-FPh-3,5-DTBS]) bileşiği ve bu bileşiklerin bakır ile paladyum komplekslerinin sitotoksik etkileri kolorimetrik olarak MTT yöntemiyle belirlendi. Bu amaçla sentezlenen altı bileşiğin 1-1000 μM aralığındaki logaritmik dozları kullanıldı. K562 hücrelerinin bileşiklerle 72 saat inkübasyondan sonra elde edilen optik dansite (OD) verilerinden yararlanılarak her bileşiğe ait IC50 değeri hesaplandı.

Bulgular: K562 hücrelerde o-FPh-3,5-DTBS bileşiğinin, p-FPh-3,5-DTBS bileşiğine kıyasla daha yüksek sitotoksik etkiye sahip olduğu tespit edilmiştir. Aynı zamanda bu bileşiklerin bakır kompleksleri, paladyum komplekslerine göre daha güçlü sitotoksik etki göstermiştir.

Sonuç: Sitotoksik etkiye sahip bu bileşikler ile yapılacak ileri düzeydeki çalışmaların faydalı olacağını düşünmektedir.

Ethical Statement

Bu çalışma için etik kurul izni gerekmemektedir

Supporting Institution

Bu çalışma Harran üniversitesi HÜBAP (Proje No: 13105) birimi tarafından desteklenmiştir.

Project Number

13105

References

  • 1. American Cancer Society. Cancer Facts & Figures. 2024. Accessed June 26, 2024. Erişim Linki: https://www.cancer.org/research/cancer-facts-statistics/all-cancer-facts-figures/cancer-facts-figures-2021.html. Erişim Tarihi:11.12.2024.
  • 2. Jabbour E, Kantarjian H. Chronic myeloid leukemia: 2025 update on diagnosis, therapy, and monitoring. Am J Hematol. 2024;99(11): 2191‐2212. doi:10.1002/ajh.27443.
  • 3. Bourne G, Bhatia R, Jamy O. Treatment-Free Remission in Chronic Myeloid Leukemia. J Clin Med. 2024;13(9): 2567-78. doi:10.3390/jcm13092567.
  • 4. Shah NP, Bhatia R, Altman JK et al. (). Chronic Myeloid Leukemia, Version 2.2024, NCCN Clinical Practice Guidelines in Oncology. J. Natl. Compr. Canc. Netw. 2024; 22(1): 43-69. doi:10.6004/jnccn.2024.0007.
  • 5. Kantarjian H, Paul S, Thakkar J, Jabbour E. The influence of drug prices, new availability of inexpensive generic imatinib, new approvals, and post-marketing research on the treatment of chronic myeloid leukaemia in the USA. Lancet Haematol. 2022;9(11): e854-e861.
  • 6. Prakash A, Adhikari D. Application of Schiff bases and their metal complexes-A Review. Int. J. ChemTech Res. 2011; 3(4): 1891-1896.
  • 7. Savalia RV, Patel AP, Trivedi PT et al. Rapid and Economic Synthesis of Schiff Base of Salicylaldehyde by Microwave Irradiation. Res. J. Chem. Sci. 2013; 3: 97–99.
  • 8. Serin S, Gök Y. Hidroksi Schiff Bazı Metal Komplekslerinin Tekstil Boyamacılığında Kullanabilirliğinin İncelenmesi. T. Kimya D.C. 1988; 12(3): 325- 331.
  • 9. Zeishen W, Zigi G, Zhenhuan Y. Synthesis, Characterization And Anticanser Activity Of L–Alanin Schiff Base Complexes Of Cooper (II), Zinc(II), An Cobalt (II) . Synth. React. Inorg. Met. Org. Chem. 1990; 20(3): 335–344.
  • 10. Dığrak M, Selvi S, Ahmedov MA, Bağcı E. 1,5-dien3ol’lerin Antimikrobiyal Etkilerinin İncelenmesi. XII. Ulusal Kimya Kongresi, Y.Y Üniversitesi Fen-Edebiyat Fakültesi Kimya Bölümü, Kongre Özetler Kitabı, Van, 1997; 677s.
  • 11. Kumar R, Singh AA, Kumar U et al. Recent advances in synthesis of heterocyclic Schiff base transition metal complexes and their antimicrobial activities especially antibacterial and antifungal. J. Mol. Struct. 2023; 1294: 136346.
  • 12. Kaushik S, Paliwal SK, Iyer MR, Patil VM. Promising Schiff bases in antiviral drug design and discovery. Med Chem Res. 2023;32(6): 1063-1076. doi: 10.1007/s00044-023-03068-0.
  • 13. Oveisi Keikha A, Shahraki S, Mansouri-Torshizi H, Dehghanian E, Heidari Majd M. Au (III) complexes of symmetrical tetradentate Schiff base ligands: Synthesis, characterization, anticancer/antioxidant potency, in silico prediction, and catalase binding properties Appl. Organomet. Chem. 2023;37(7):e7139. doi:10.1002/aoc.7139.
  • 14. Keikha AO, Mansouri-Torshizi H, Shahraki S, Dehghanian E. Zn (II) and Pd (II) complexes derived from novel benzohydrazide-based Schiff base ligand as multi-target agents J. Mol. Liq. 2023;391(Part A):123272. doi:10.1016/j.molliq.2023.123272.
  • 15. Shahraki S. Schiff base compounds as artificial metalloenzymes. Colloids Surf B Biointerfaces. 2022; 218:112727. doi: 10.1016/j.colsurfb.2022.112727.
  • 16. Damena T, Zeleke D, Desalegn T, Demissie TB, Eswaramoorthy R. Synthesis, characterization, and biological activities of novel vanadium (IV) and cobalt (II) complexes. ACS Omega. 2022;7:4389-4404.
  • 17. Shahraki S, Vaziri E, Saboury AA, Fan K. Biomedical potential of nanozymes: Harnessing redox enzyme mimicry for theranostic applications. Coord. Chem. Rev. 2024;517:215937. doi:10.1016/j.ccr.2024.215937.
  • 18. Barani O, Shahraki S, Nezami ZS, Delarami HS, E. Sanchooli Unveiling the molecular association of novel benzohydrazidesubstituted Schiff base complexes with human serum albümin. Inorg. Chem. Commun. 2024;162:112200.
  • 19. Shahraki K, Shahraki S, Nezami ZS, Delarami HS. New acetohydrazide-based Schiff base complexes with the ability to enhance catalase activity. Inorg. Chem. Commun. 2024;163:112318. doi:.1016/j.inoche.2024.112200.
  • 20. Shahraki S, Majd MH, Heydari A. Novel tetradentate Schiff base zinc (II) complex as a potential antioxidant and cancer chemotherapeutic agent: Insights from the photophysical and computational approach. J. Mol. Struct. 2019;1177:536-544.
  • 21. Matela G. Schiff Bases and Complexes: A Review on Anti-Cancer Activity. Anticancer Agents Med Chem. 2020;20(16):1908-1917. doi: 10.2174/1871520620666200507091207.
  • 22. Yılmaz ZK, Özdemir Ö, Aslim B, Suludere Z, Şahin E. A new bio-active asymmetric-Schiff base: synthesis and evaluation of calf thymus DNA interaction, topoisomerase IIα inhibition, in vitro antiproliferative activity, SEM analysis and molecular docking studies. J Biomol Struct Dyn. 2023;41(7):2804-2822. doi: 10.1080/07391102. 2022.2039297.
  • 23. Alvero AB, Chen W, Sartorelli AC et al. Triapine (3-amino- 2-carboxaldehyde thiosemicarbazone) Induces Apoptosis in Ovarian Cancer Cells. J. Soc. Gynecol. Investig. 2006;13:145–152. doi: 10.1016/j.jsgi.2005.11.004.
  • 24. Niu ZX, Hu J, Sun JF, Wang YT. Fluorine in the pharmaceutical industry: Synthetic approaches and application of clinically approved fluorine-enriched anti-infectious medications. Eur J Med Chem. 2024;271:116446. doi: 10.1016/j.ejmech.2024.116446.
  • 25. Zakaria N, Kandile NG, Mohamed MI, Zaky HT, Mohamed HM. Superior remedy colon cancer HCT-116 cells via new chitosan Schiff base nanocomposites: Synthesis and characterization. Int J Biol Macromol. 2024; 281(Pt 1): 135916. doi:10.1016/j.ijbiomac.2024.135916.
  • 26. Podolski-Renić A, Čipak Gašparović A, Valente A et al. Schiff bases and their metal complexes to target and overcome (multidrug) resistance in cancer. Eur J Med Chem. 2024; 270:116363. doi: 10.1016/j.ejmech. 2024.116363.
  • 27. Chen S, Liu X, Ge X et al., Lysosome-targeted iridium (III) compounds with pyridine-triphenylamine Schiff base ligands: syntheses, antitumor applications and mechanisms. Inorg. Chem. Front. 2020;7:91–100. doi:10.1039/C9QI01161G.
  • 28. Nemat A, Khan IN, Kalsoom S. et al., Synthesis, anticancer evaluation and molecular docking studies of methotrexate's novel Schiff base derivatives against malignant glioma cell lines. J. Biomol. Struct. Dyn. 2022;40:2865–2877. doi:10.1080/07391102.2020.1844053.
  • 29. Osowole, AA, Akpan EJ,. Synthesis, Spectroscopic Characterisation, İn-Vitro Anticancer And Antimicrobial and Properties of Some Metal(II) Complexes of 3-{4,6-dimethoxypyrimidinyl) imino methyl}naphthalen-2-ol. Eur. J. Appl. Sci. 2012; 4(1):14-20. doi:10.9734/IRJPAC/2012/1540.
  • 30. Oveisi Keikha A, Shahraki S, Dehghanian E, Mansouri-Torshizi H. Effect of central metal ion on some pharmacological properties of new Schiff base complexes. Anticancer, antioxidant, kinetic/thermodynamic and computational studies. Spectrochim. Acta A Mol. Biomol. Spectrosc. 2025;325:125034. doi: 10.1016/j.saa.2024.125034.

Anticancer Activities of Fluorinated Shiff Base Ligands and Their Copper and Palladium Complexes on Human Chronic Myeloid Leukemia Cells

Year 2026, Volume: 10 Issue: 1 , 79 - 87 , 29.04.2026
https://doi.org/10.46332/aemj.1637016
https://izlik.org/JA97AN98MX

Abstract

Purpose: The emergence of side effects due to chemotherapeutics in cancer treatment and the development of drug resistance are among the most important problems. In order to overcome these difficulties, the need for new anticancer agent research increases. In recent years, data indicating that Schiff bases have anticancer activity has attracted attention. It is reported that these compounds
cause cell death by inducing apoptosis in cancer cells and prevent cell proliferation by stopping DNA and RNA synthesis. In the study, the cytotoxic effects of fluorinated Schiff bases and their copper and palladium complexes on human chronic myeloid leukemia cells were investigated.

Materials and Methods: Cytotoxic effects of fluorine-containing Schiff bases (o-fluorophenyl-3,5-di-tert-butylsalicylaldimine [oFPh-3,5-DTBS] and p-fluorophenyl-3,5-di-tert-butylsalicylaldimine [o-FPh-3,5-DTBS]) and their copper and palladium complexes were determined colorimetrically by the MTT method. For this purpose, logarithmic doses of each of the six compounds synthesized
in the range of 1-1000 μM were used. IC50values of each compound were calculated using the OD data obtained after 72 hours of incubation of K562 cells with the compounds.

Results: The cytotoxic effect of o-FPh-3,5-DTBS on K562 cells was determined to be higher compared to p-FPh-3,5-DTBS. At the same time, copper complexes of Schiff bases showed stronger cytotoxic effects on K562 cells, while this effect was found to be weak in palladium complexes.

Conclusion: We believe that further research on compounds with high cytotoxic effects may yield useful results.

Ethical Statement

Ethics committee approval is not required for this study

Project Number

13105

References

  • 1. American Cancer Society. Cancer Facts & Figures. 2024. Accessed June 26, 2024. Erişim Linki: https://www.cancer.org/research/cancer-facts-statistics/all-cancer-facts-figures/cancer-facts-figures-2021.html. Erişim Tarihi:11.12.2024.
  • 2. Jabbour E, Kantarjian H. Chronic myeloid leukemia: 2025 update on diagnosis, therapy, and monitoring. Am J Hematol. 2024;99(11): 2191‐2212. doi:10.1002/ajh.27443.
  • 3. Bourne G, Bhatia R, Jamy O. Treatment-Free Remission in Chronic Myeloid Leukemia. J Clin Med. 2024;13(9): 2567-78. doi:10.3390/jcm13092567.
  • 4. Shah NP, Bhatia R, Altman JK et al. (). Chronic Myeloid Leukemia, Version 2.2024, NCCN Clinical Practice Guidelines in Oncology. J. Natl. Compr. Canc. Netw. 2024; 22(1): 43-69. doi:10.6004/jnccn.2024.0007.
  • 5. Kantarjian H, Paul S, Thakkar J, Jabbour E. The influence of drug prices, new availability of inexpensive generic imatinib, new approvals, and post-marketing research on the treatment of chronic myeloid leukaemia in the USA. Lancet Haematol. 2022;9(11): e854-e861.
  • 6. Prakash A, Adhikari D. Application of Schiff bases and their metal complexes-A Review. Int. J. ChemTech Res. 2011; 3(4): 1891-1896.
  • 7. Savalia RV, Patel AP, Trivedi PT et al. Rapid and Economic Synthesis of Schiff Base of Salicylaldehyde by Microwave Irradiation. Res. J. Chem. Sci. 2013; 3: 97–99.
  • 8. Serin S, Gök Y. Hidroksi Schiff Bazı Metal Komplekslerinin Tekstil Boyamacılığında Kullanabilirliğinin İncelenmesi. T. Kimya D.C. 1988; 12(3): 325- 331.
  • 9. Zeishen W, Zigi G, Zhenhuan Y. Synthesis, Characterization And Anticanser Activity Of L–Alanin Schiff Base Complexes Of Cooper (II), Zinc(II), An Cobalt (II) . Synth. React. Inorg. Met. Org. Chem. 1990; 20(3): 335–344.
  • 10. Dığrak M, Selvi S, Ahmedov MA, Bağcı E. 1,5-dien3ol’lerin Antimikrobiyal Etkilerinin İncelenmesi. XII. Ulusal Kimya Kongresi, Y.Y Üniversitesi Fen-Edebiyat Fakültesi Kimya Bölümü, Kongre Özetler Kitabı, Van, 1997; 677s.
  • 11. Kumar R, Singh AA, Kumar U et al. Recent advances in synthesis of heterocyclic Schiff base transition metal complexes and their antimicrobial activities especially antibacterial and antifungal. J. Mol. Struct. 2023; 1294: 136346.
  • 12. Kaushik S, Paliwal SK, Iyer MR, Patil VM. Promising Schiff bases in antiviral drug design and discovery. Med Chem Res. 2023;32(6): 1063-1076. doi: 10.1007/s00044-023-03068-0.
  • 13. Oveisi Keikha A, Shahraki S, Mansouri-Torshizi H, Dehghanian E, Heidari Majd M. Au (III) complexes of symmetrical tetradentate Schiff base ligands: Synthesis, characterization, anticancer/antioxidant potency, in silico prediction, and catalase binding properties Appl. Organomet. Chem. 2023;37(7):e7139. doi:10.1002/aoc.7139.
  • 14. Keikha AO, Mansouri-Torshizi H, Shahraki S, Dehghanian E. Zn (II) and Pd (II) complexes derived from novel benzohydrazide-based Schiff base ligand as multi-target agents J. Mol. Liq. 2023;391(Part A):123272. doi:10.1016/j.molliq.2023.123272.
  • 15. Shahraki S. Schiff base compounds as artificial metalloenzymes. Colloids Surf B Biointerfaces. 2022; 218:112727. doi: 10.1016/j.colsurfb.2022.112727.
  • 16. Damena T, Zeleke D, Desalegn T, Demissie TB, Eswaramoorthy R. Synthesis, characterization, and biological activities of novel vanadium (IV) and cobalt (II) complexes. ACS Omega. 2022;7:4389-4404.
  • 17. Shahraki S, Vaziri E, Saboury AA, Fan K. Biomedical potential of nanozymes: Harnessing redox enzyme mimicry for theranostic applications. Coord. Chem. Rev. 2024;517:215937. doi:10.1016/j.ccr.2024.215937.
  • 18. Barani O, Shahraki S, Nezami ZS, Delarami HS, E. Sanchooli Unveiling the molecular association of novel benzohydrazidesubstituted Schiff base complexes with human serum albümin. Inorg. Chem. Commun. 2024;162:112200.
  • 19. Shahraki K, Shahraki S, Nezami ZS, Delarami HS. New acetohydrazide-based Schiff base complexes with the ability to enhance catalase activity. Inorg. Chem. Commun. 2024;163:112318. doi:.1016/j.inoche.2024.112200.
  • 20. Shahraki S, Majd MH, Heydari A. Novel tetradentate Schiff base zinc (II) complex as a potential antioxidant and cancer chemotherapeutic agent: Insights from the photophysical and computational approach. J. Mol. Struct. 2019;1177:536-544.
  • 21. Matela G. Schiff Bases and Complexes: A Review on Anti-Cancer Activity. Anticancer Agents Med Chem. 2020;20(16):1908-1917. doi: 10.2174/1871520620666200507091207.
  • 22. Yılmaz ZK, Özdemir Ö, Aslim B, Suludere Z, Şahin E. A new bio-active asymmetric-Schiff base: synthesis and evaluation of calf thymus DNA interaction, topoisomerase IIα inhibition, in vitro antiproliferative activity, SEM analysis and molecular docking studies. J Biomol Struct Dyn. 2023;41(7):2804-2822. doi: 10.1080/07391102. 2022.2039297.
  • 23. Alvero AB, Chen W, Sartorelli AC et al. Triapine (3-amino- 2-carboxaldehyde thiosemicarbazone) Induces Apoptosis in Ovarian Cancer Cells. J. Soc. Gynecol. Investig. 2006;13:145–152. doi: 10.1016/j.jsgi.2005.11.004.
  • 24. Niu ZX, Hu J, Sun JF, Wang YT. Fluorine in the pharmaceutical industry: Synthetic approaches and application of clinically approved fluorine-enriched anti-infectious medications. Eur J Med Chem. 2024;271:116446. doi: 10.1016/j.ejmech.2024.116446.
  • 25. Zakaria N, Kandile NG, Mohamed MI, Zaky HT, Mohamed HM. Superior remedy colon cancer HCT-116 cells via new chitosan Schiff base nanocomposites: Synthesis and characterization. Int J Biol Macromol. 2024; 281(Pt 1): 135916. doi:10.1016/j.ijbiomac.2024.135916.
  • 26. Podolski-Renić A, Čipak Gašparović A, Valente A et al. Schiff bases and their metal complexes to target and overcome (multidrug) resistance in cancer. Eur J Med Chem. 2024; 270:116363. doi: 10.1016/j.ejmech. 2024.116363.
  • 27. Chen S, Liu X, Ge X et al., Lysosome-targeted iridium (III) compounds with pyridine-triphenylamine Schiff base ligands: syntheses, antitumor applications and mechanisms. Inorg. Chem. Front. 2020;7:91–100. doi:10.1039/C9QI01161G.
  • 28. Nemat A, Khan IN, Kalsoom S. et al., Synthesis, anticancer evaluation and molecular docking studies of methotrexate's novel Schiff base derivatives against malignant glioma cell lines. J. Biomol. Struct. Dyn. 2022;40:2865–2877. doi:10.1080/07391102.2020.1844053.
  • 29. Osowole, AA, Akpan EJ,. Synthesis, Spectroscopic Characterisation, İn-Vitro Anticancer And Antimicrobial and Properties of Some Metal(II) Complexes of 3-{4,6-dimethoxypyrimidinyl) imino methyl}naphthalen-2-ol. Eur. J. Appl. Sci. 2012; 4(1):14-20. doi:10.9734/IRJPAC/2012/1540.
  • 30. Oveisi Keikha A, Shahraki S, Dehghanian E, Mansouri-Torshizi H. Effect of central metal ion on some pharmacological properties of new Schiff base complexes. Anticancer, antioxidant, kinetic/thermodynamic and computational studies. Spectrochim. Acta A Mol. Biomol. Spectrosc. 2025;325:125034. doi: 10.1016/j.saa.2024.125034.
There are 30 citations in total.

Details

Primary Language Turkish
Subjects Clinical Chemistry, Clinical Oncology
Journal Section Research Article
Authors

Faruk Süzergöz 0000-0001-5000-0998

Yusuf Variş This is me 0009-0002-1655-836X

Nilgün Okşak 0000-0002-6058-9414

Mustafa Ünal Boyraz 0000-0002-5455-0353

Bestoon Shekhany This is me 0000-0001-8849-4153

Veli Kasım 0000-0001-5704-7801

Project Number 13105
Submission Date February 10, 2025
Acceptance Date January 2, 2026
Publication Date April 29, 2026
DOI https://doi.org/10.46332/aemj.1637016
IZ https://izlik.org/JA97AN98MX
Published in Issue Year 2026 Volume: 10 Issue: 1

Cite

APA Süzergöz, F., Variş, Y., Okşak, N., Boyraz, M. Ü., Shekhany, B., & Kasım, V. (2026). İnsan Kronik Myeloid Lösemi Hücreleri Üzerine Florlu Shiff Bazı Ligandları ile Bunların Bakır ve Paladyum Komplekslerinin Antikanser Aktiviteleri. Ahi Evran Medical Journal, 10(1), 79-87. https://doi.org/10.46332/aemj.1637016
AMA 1.Süzergöz F, Variş Y, Okşak N, Boyraz MÜ, Shekhany B, Kasım V. İnsan Kronik Myeloid Lösemi Hücreleri Üzerine Florlu Shiff Bazı Ligandları ile Bunların Bakır ve Paladyum Komplekslerinin Antikanser Aktiviteleri. Ahi Evran Med J. 2026;10(1):79-87. doi:10.46332/aemj.1637016
Chicago Süzergöz, Faruk, Yusuf Variş, Nilgün Okşak, Mustafa Ünal Boyraz, Bestoon Shekhany, and Veli Kasım. 2026. “İnsan Kronik Myeloid Lösemi Hücreleri Üzerine Florlu Shiff Bazı Ligandları Ile Bunların Bakır Ve Paladyum Komplekslerinin Antikanser Aktiviteleri”. Ahi Evran Medical Journal 10 (1): 79-87. https://doi.org/10.46332/aemj.1637016.
EndNote Süzergöz F, Variş Y, Okşak N, Boyraz MÜ, Shekhany B, Kasım V (April 1, 2026) İnsan Kronik Myeloid Lösemi Hücreleri Üzerine Florlu Shiff Bazı Ligandları ile Bunların Bakır ve Paladyum Komplekslerinin Antikanser Aktiviteleri. Ahi Evran Medical Journal 10 1 79–87.
IEEE [1]F. Süzergöz, Y. Variş, N. Okşak, M. Ü. Boyraz, B. Shekhany, and V. Kasım, “İnsan Kronik Myeloid Lösemi Hücreleri Üzerine Florlu Shiff Bazı Ligandları ile Bunların Bakır ve Paladyum Komplekslerinin Antikanser Aktiviteleri”, Ahi Evran Med J, vol. 10, no. 1, pp. 79–87, Apr. 2026, doi: 10.46332/aemj.1637016.
ISNAD Süzergöz, Faruk - Variş, Yusuf - Okşak, Nilgün - Boyraz, Mustafa Ünal - Shekhany, Bestoon - Kasım, Veli. “İnsan Kronik Myeloid Lösemi Hücreleri Üzerine Florlu Shiff Bazı Ligandları Ile Bunların Bakır Ve Paladyum Komplekslerinin Antikanser Aktiviteleri”. Ahi Evran Medical Journal 10/1 (April 1, 2026): 79-87. https://doi.org/10.46332/aemj.1637016.
JAMA 1.Süzergöz F, Variş Y, Okşak N, Boyraz MÜ, Shekhany B, Kasım V. İnsan Kronik Myeloid Lösemi Hücreleri Üzerine Florlu Shiff Bazı Ligandları ile Bunların Bakır ve Paladyum Komplekslerinin Antikanser Aktiviteleri. Ahi Evran Med J. 2026;10:79–87.
MLA Süzergöz, Faruk, et al. “İnsan Kronik Myeloid Lösemi Hücreleri Üzerine Florlu Shiff Bazı Ligandları Ile Bunların Bakır Ve Paladyum Komplekslerinin Antikanser Aktiviteleri”. Ahi Evran Medical Journal, vol. 10, no. 1, Apr. 2026, pp. 79-87, doi:10.46332/aemj.1637016.
Vancouver 1.Faruk Süzergöz, Yusuf Variş, Nilgün Okşak, Mustafa Ünal Boyraz, Bestoon Shekhany, Veli Kasım. İnsan Kronik Myeloid Lösemi Hücreleri Üzerine Florlu Shiff Bazı Ligandları ile Bunların Bakır ve Paladyum Komplekslerinin Antikanser Aktiviteleri. Ahi Evran Med J. 2026 Apr. 1;10(1):79-87. doi:10.46332/aemj.1637016

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