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GENOMİK BİYOBELİRTEÇLER KULLANILARAK HBV VE HCV İLE İLİŞKİLİ HEPATOSELLÜLER KARSİNOMUN MAKİNE ÖĞRENİMİ TABANLI SINIFLANDIRILMASI

Year 2022, Volume: 85 Issue: 4, 532 - 540, 28.10.2022
https://doi.org/10.26650/IUITFD.1130442

Abstract

Amaç: Hepatoselüler karsinomun (HCC) optimal yönetimi için altında yatan nedenleri bilmek çok önemlidir. Bu çalışma, HBV veya HCV enfeksiyonu olan HCC hastalarının açık erişim gen ekspresyon verilerini XGboost yöntemini kullanarak sınıflandırmayı amaçlamaktadır. Gereç ve Yöntem: Bu vaka-kontrol çalışmasında, HBV ve HCV ile ilişkili HCC’li hastaların açık erişimli gen ekspresyonu verileri dikkate alınmıştır. Bu amaçla, 17 HBV+HCC ve 17 HCV+HCC hastadan elde edilen veriler çalışmaya dahil edildi. Sınıflandırma için on katlı çapraz geçerlilik kullanılarak XGboost modeli oluşturuldu. Model performansı için doğruluk, dengeli doğruluk, duyarlılık, özgüllük, pozitif tahmin değeri ve negatif tahmin değeri ve F1 skor performans metrikleri değerlendirildi. Bulgular: Özellik seçimi yaklaşımı ile 17 gen seçilmiş ve bu girdi değişkenleri kullanılarak modelleme yapılmıştır. XGboost modelinden elde edilen doğruluk, dengeli doğruluk, duyarlılık, özgüllük, pozitif tahmin değeri, negatif tahmin değeri ve F1 skor sırasıyla %97,1, %97,1, %94,1, %100, %100, %94,4 ve %97 idi. XGboost’tan elde edilen değişken önemliliği bulgularına dayanarak, ALDOC, GLUD2, TRAPPC10, FLJ12998, RPL39, KDELR2 ve KIAA0446 genleri, HBV ile ilişkili HCC için potansiyel biyobelirteçler olarak kullanılabilir. Sonuç: Çalışma sonucunda, HCC’ye neden olan iki farklı etiyolojik faktör (HBV ve HCV), makine öğrenimi tabanlı bir tahmin yaklaşımı kullanılarak sınıflandırıldı ve HBV ile ilişkili HCC için biyobelirteç olabilecek genler tanımlandı. Ortaya çıkan genler sonraki araştırmalarda klinik olarak doğrulandıktan sonra, bu genlere dayalı terapötik prosedürler oluşturulabilir ve klinik uygulamada kullanımları belgelenebilir. Anahtar Kelimeler: 

References

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MACHINE LEARNING-BASED CLASSIFICATION OF HBV AND HCV-RELATED HEPATOCELLULAR CARCINOMA USING GENOMIC BIOMARKERS

Year 2022, Volume: 85 Issue: 4, 532 - 540, 28.10.2022
https://doi.org/10.26650/IUITFD.1130442

Abstract

Objective: It is crucial to know the underlying causes of hepatocellular carcinoma (HCC) for optimal management. This study aims to classify open access gene expression data of HCC patients who have an HBV or HCV infection using the XGboost method. Material and Methods: This case-control study considered the open-access gene expression data of patients with HBV-related HCC and HCV-related HCC. For this purpose, data from 17 patients with HBV+HCC and 17 patients with HCV+HCC were included. XGboost was constructed for the classification via tenfold cross-validation. Accuracy, balanced accuracy, sensitivity, specificity, the positive predictive value, the negative predictive value, and F1 score performance metrics were evaluated for a model performance. Results: With the feature selection approach, 17 genes were chosen, and modeling was done using these input variables. Accuracy, balanced accuracy, sensitivity, specificity, positive predictive value, negative predictive value, and the F1 score obtained from the XGboost model were 97.1%, 97.1%, 94.1%, 100%, 100%, 94.4%, and 97%, respectively. Based on the variable importance findings from the XGboost, the ALDOC, GLUD2, TRAPPC10, FLJ12998, RPL39, KDELR2, and KIAA0446 genes can be employed as potential biomarkers for HBV-related HCC. Conclusion: As a result of the study, two different etiological factors (HBV and HCV) causing HCC were classified using a machine learning-based prediction approach, and genes that could be biomarkers for HBV-related HCC were identified. After the resulting genes have been clinically validated in subsequent research, therapeutic procedures based on these genes can be established and their utility in clinical practice documented. 

References

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  • 3. Sayiner M, Golabi P, Younossi ZM. Disease burden of hepatocellular carcinoma: a global perspective. Dig Dis Sci 2019;64(4):910-7. [CrossRef] google scholar
  • 4. Levrero M, Zucman-Rossi J. Mechanisms of HBV-induced hepatocellular carcinoma. J Hepatol 2016;64(1 Suppl):S84-101. [CrossRef] google scholar
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  • 8. Ming L, Thorgeirsson SS, Gail MH, Lu P, Harris CC, Wang N, et al. Dominant role of hepatitis B virus and cofactor role of aflatoxin in hepatocarcinogenesis in Qidong, China. Hepatology 2002;36(5):1214-20. [CrossRef] google scholar
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  • 13. El-Serag HB. Epidemiologyofviralhepatitis andhepatocellular carcinoma. Gastroenterology 2012;142(6):1264-73. [CrossRef] google scholar
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  • 17. Polikar R. Ensemble learning. Ensemble machine learning. Springer; 2012: pp. 1-34. [CrossRef] google scholar
  • 18. Akman M, Genç Y, Ankarali H. Random forests yöntemi ve saglık alanında bir uygulama/Random forests methods and an application in health science. Turkiye Klinikleri J Biostat 2011;3(1):36-48. google scholar
  • 19. Pinero F, Dirchwolf M, Pessoa MG. Biomarkers in hepatocellular carcinoma: diagnosis, prognosis and treatment response assessment. Cells 2020;9(6):1370. [CrossRef] google scholar
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  • 23. Ueda T, Honda M, Horimoto K, Aburatani S, Saito S, Yamashita T, et al. Gene expression profiling of hepatitis B-and hepatitis C-related hepatocellular carcinoma using graphical Gaussian modeling. Genomics 2013;101(4):238-48. [CrossRef] google scholar
  • 24. Chang HY, Thomson JA, Chen X. Microarray analysis of stem cells and differentiation. Methods Enzymol 2006;420:225-54. [CrossRef] google scholar
  • 25. Saeys Y, Inza I, Larranaga P. A review of feature selection techniques in bioinformatics. Bioinformatics 2007;23(19):2507-17. [CrossRef] google scholar
  • 26. Fodor IK. A Survey of Dimension Reduction Techniques. Lawrence Livermore National Lab (CA). Department of Energy (US). 2002 May. Report No: UCRL-ID-148494 TRN: US200408%%150. [CrossRef] google scholar
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  • 28. Wang J, Li P, Ran R, Che Y, Zhou Y. A short-term photovoltaic power prediction model based on the gradient boost decision tree. Appl Sci 2018;8(5):689. [CrossRef] google scholar
  • 29. Salam Patrous Z. Evaluating XGBoost for User Classification by using Behavioral Features Extracted from Smartphone Sensors (dissertation). Stockholm: KTH Royal Institute of Technology. 2018. google scholar
  • 30. Dikker J. Boosted tree learning for balanced item recommendation in online retail (dissertation). Eindhoven: The Eindhoven University of Technology. 2017. google scholar
  • 31. Smyth GK. Limma: linear models for microarray data. Bioinformatics and computational biology solutions using R and Bioconductor. In: Gail M, Samet JM. Statistics for Biology and Health. Springer; 2005: pp. 397-420. [CrossRef] google scholar
  • 32. Yan H, Zheng G, Qu J, Liu Y, Huang X, Zhang E, et al. Identification of key candidate genes and pathways in multiple myeloma by integrated bioinformatics analysis. J Cell Physiol 2019; 234(12):23785-97. [CrossRef] google scholar
  • 33. Cevallos M, Egger M, Moher D. STROBE (Strengthening the Reporting of Observational Studies in Epidemiology). In: Moher D, Altman DG, Schulz KF, Simera I, Wager E, editors. Guidelines for Reporting Health Research: A User’s Manual. John Wiley & Sons, Ltd; 2014. p. 169-79. [CrossRef] google scholar
  • 34. Yang JD, Hainaut P, Gores GJ, Amadou A, Plymoth A, Roberts LR. A global view of hepatocellular carcinoma: trends, risk, prevention and management. Nat Rev Gastroenterol Hepatol 2019;16(10):589-604. [CrossRef] google scholar
  • 35. Tang A, Hallouch O, Chernyak V, Kamaya A, Sirlin CB. Epidemiology of hepatocellular carcinoma: target population for surveillance and diagnosis. Abdom Radiol (NY) 2018;43(1):13-25. [CrossRef] google scholar
  • 36. Park JW, Chen M, Colombo M, Roberts LR, Schwartz M, Chen PJ, et al. Global patterns of hepatocellular carcinoma management from diagnosis to death: the BRIDGE Study. Liver Int 2015;35(9):2155-66. [CrossRef] google scholar
  • 37. Yang JD, Gyedu A, Afihene MY, Duduyemi BM, Micah E, Kingham PT, et al. Hepatocellular carcinoma occurs at an earlier age in Africans, particularly in association with chronic hepatitis B. Am J Gastroenterol 2015;110(11):1629-31. [CrossRef] google scholar
  • 38. Jefferies M, Rauff B, Rashid H, Lam T, Rafiq S. Update on global epidemiology of viral hepatitis and preventive strategies. World J Clin Cases 2018;6(13):589-99. [CrossRef] google scholar
  • 39. Hill AM, Nath S, Simmons B. The road to elimination of hepatitis C: analysis of cures versus new infections in 91 countries. J Virus Erad 2017;3(3):117-23. [CrossRef] google scholar
  • 40. Marshall AD, Pawlotsky J-M, Lazarus JV, Aghemo A, Dore GJ, Grebely J. The removal of DAA restrictions in Europe-one step closer to eliminating HCV as a major public health threat. J Hepatol 2018;69(5):1188-96. [CrossRef] google scholar
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  • 42. Ghidini M, Braconi C. Non-coding RNAs in primary liver cancer. Front Med (Lausanne) 2015;2:36. [CrossRef] google scholar
  • 43. Xie Q, Fan F, Wei W, Liu Y, Xu Z, Zhai L, et al. Multi-omics analyses reveal metabolic alterations regulated by hepatitis B virus core protein in hepatocellular carcinoma cells. Sci Rep 2017;7(1):41089. [CrossRef] google scholar
  • 44. Li H, Zhu W, Zhang L, Lei H, Wu X, Guo L, et al. The metabolic responses to hepatitis B virus infection shed new light on pathogenesis and targets for treatment. Sci Rep 2015;5(1):8421. [CrossRef] google scholar
  • 45. Gao Q, Zhu H, Dong L, Shi W, Chen R, Song Z, et al. Integrated proteogenomic characterization of HBV-related hepatocellular carcinoma. Cell 2019;179(2):561-77. [CrossRef] google scholar
  • 46. Wei X, Su R, Yang M, Pan B, Lu J, Lin H, et al. Quantitative proteomic profiling of hepatocellular carcinoma at different serum alpha-fetoprotein level. Translational oncology 2022;20:101422. [CrossRef] google scholar
  • 47. Lu M, Kong X, Wang H, Huang G, Ye C, He Z. A novel microRNAs expression signature for hepatocellular carcinoma diagnosis and prognosis. Oncotarget 2017;8(5):8775-84. [CrossRef] google scholar
  • 48. El Khoury W, Nasr Z. Deregulation of ribosomal proteins in human cancers. Biosci Rep 2021;41(12):BSR20211577. [CrossRef] google scholar
  • 49. Li F, Deng Y, Zhang S, Zhu B, Wang J, Wang J, et al. Human hepatocyte-enriched miRNA-192-3p promotes HBV replication through inhibiting Akt/mTOR signalling by targeting ZNF143 in hepatic cell lines. Emerg Microbes Infect 2022;11(1):616-28. [CrossRef] google scholar
  • 50. Akbulut S, Garzali IU, Hargura AS, Aloun A, Yilmaz S. Screening, Surveillance, and Management of Hepatocellular Carcinoma During the COVID-19 Pandemic: a Narrative Review. J Gastrointest Cancer 2022:1-12. [CrossRef] google scholar
There are 50 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section RESEARCH
Authors

Sami Akbulut 0000-0002-6864-7711

Zeynep Küçükakçalı 0000-0001-7956-9272

Cemil Çolak 0000-0001-5406-098X

Publication Date October 28, 2022
Submission Date June 14, 2022
Published in Issue Year 2022 Volume: 85 Issue: 4

Cite

APA Akbulut, S., Küçükakçalı, Z., & Çolak, C. (2022). MACHINE LEARNING-BASED CLASSIFICATION OF HBV AND HCV-RELATED HEPATOCELLULAR CARCINOMA USING GENOMIC BIOMARKERS. Journal of Istanbul Faculty of Medicine, 85(4), 532-540. https://doi.org/10.26650/IUITFD.1130442
AMA Akbulut S, Küçükakçalı Z, Çolak C. MACHINE LEARNING-BASED CLASSIFICATION OF HBV AND HCV-RELATED HEPATOCELLULAR CARCINOMA USING GENOMIC BIOMARKERS. İst Tıp Fak Derg. October 2022;85(4):532-540. doi:10.26650/IUITFD.1130442
Chicago Akbulut, Sami, Zeynep Küçükakçalı, and Cemil Çolak. “MACHINE LEARNING-BASED CLASSIFICATION OF HBV AND HCV-RELATED HEPATOCELLULAR CARCINOMA USING GENOMIC BIOMARKERS”. Journal of Istanbul Faculty of Medicine 85, no. 4 (October 2022): 532-40. https://doi.org/10.26650/IUITFD.1130442.
EndNote Akbulut S, Küçükakçalı Z, Çolak C (October 1, 2022) MACHINE LEARNING-BASED CLASSIFICATION OF HBV AND HCV-RELATED HEPATOCELLULAR CARCINOMA USING GENOMIC BIOMARKERS. Journal of Istanbul Faculty of Medicine 85 4 532–540.
IEEE S. Akbulut, Z. Küçükakçalı, and C. Çolak, “MACHINE LEARNING-BASED CLASSIFICATION OF HBV AND HCV-RELATED HEPATOCELLULAR CARCINOMA USING GENOMIC BIOMARKERS”, İst Tıp Fak Derg, vol. 85, no. 4, pp. 532–540, 2022, doi: 10.26650/IUITFD.1130442.
ISNAD Akbulut, Sami et al. “MACHINE LEARNING-BASED CLASSIFICATION OF HBV AND HCV-RELATED HEPATOCELLULAR CARCINOMA USING GENOMIC BIOMARKERS”. Journal of Istanbul Faculty of Medicine 85/4 (October 2022), 532-540. https://doi.org/10.26650/IUITFD.1130442.
JAMA Akbulut S, Küçükakçalı Z, Çolak C. MACHINE LEARNING-BASED CLASSIFICATION OF HBV AND HCV-RELATED HEPATOCELLULAR CARCINOMA USING GENOMIC BIOMARKERS. İst Tıp Fak Derg. 2022;85:532–540.
MLA Akbulut, Sami et al. “MACHINE LEARNING-BASED CLASSIFICATION OF HBV AND HCV-RELATED HEPATOCELLULAR CARCINOMA USING GENOMIC BIOMARKERS”. Journal of Istanbul Faculty of Medicine, vol. 85, no. 4, 2022, pp. 532-40, doi:10.26650/IUITFD.1130442.
Vancouver Akbulut S, Küçükakçalı Z, Çolak C. MACHINE LEARNING-BASED CLASSIFICATION OF HBV AND HCV-RELATED HEPATOCELLULAR CARCINOMA USING GENOMIC BIOMARKERS. İst Tıp Fak Derg. 2022;85(4):532-40.

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