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Artificial intelligence-based prediction of molecular and genetic markers for hepatitis C–related hepatocellular carcinoma

BACKGROUND: Hepatocellular carcinoma (HCC) is the main cause of mortality from cancer globally. This paper intends to classify public gene expression data of patients with Hepatitis C virus-related HCC (HCV+HCC) and chronic HCV without HCC (HCV alone) through the XGboost approach and to identify key...

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Autores principales: Colak, Cemil, Kucukakcali, Zeynep, Akbulut, Sami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553079/
https://www.ncbi.nlm.nih.gov/pubmed/37811067
http://dx.doi.org/10.1097/MS9.0000000000001210
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author Colak, Cemil
Kucukakcali, Zeynep
Akbulut, Sami
author_facet Colak, Cemil
Kucukakcali, Zeynep
Akbulut, Sami
author_sort Colak, Cemil
collection PubMed
description BACKGROUND: Hepatocellular carcinoma (HCC) is the main cause of mortality from cancer globally. This paper intends to classify public gene expression data of patients with Hepatitis C virus-related HCC (HCV+HCC) and chronic HCV without HCC (HCV alone) through the XGboost approach and to identify key genes that may be responsible for HCC. METHODS: The current research is a retrospective case–control study. Public data from 17 patients with HCV+HCC and 35 patients with HCV-alone samples were used in this study. An XGboost model was established for the classification by 10-fold cross-validation. Accuracy (AC), balanced accuracy (BAC), sensitivity, specificity, positive predictive value, negative predictive value, and F1 score were utilized for performance assessment. RESULTS: AC, BAC, sensitivity, specificity, positive predictive value, negative predictive value, and F1 scores from the XGboost model were 98.1, 97.1, 100, 94.1, 97.2, 100, and 98.6%, respectively. According to the variable importance values from the XGboost, the HAO2, TOMM20, GPC3, and PSMB4 genes can be considered potential biomarkers for HCV-related HCC. CONCLUSION: A machine learning-based prediction method discovered genes that potentially serve as biomarkers for HCV-related HCC. After clinical confirmation of the acquired genes in the following medical study, their therapeutic use can be established. Additionally, more detailed clinical works are needed to substantiate the significant conclusions in the current study.
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spelling pubmed-105530792023-10-06 Artificial intelligence-based prediction of molecular and genetic markers for hepatitis C–related hepatocellular carcinoma Colak, Cemil Kucukakcali, Zeynep Akbulut, Sami Ann Med Surg (Lond) Original Research BACKGROUND: Hepatocellular carcinoma (HCC) is the main cause of mortality from cancer globally. This paper intends to classify public gene expression data of patients with Hepatitis C virus-related HCC (HCV+HCC) and chronic HCV without HCC (HCV alone) through the XGboost approach and to identify key genes that may be responsible for HCC. METHODS: The current research is a retrospective case–control study. Public data from 17 patients with HCV+HCC and 35 patients with HCV-alone samples were used in this study. An XGboost model was established for the classification by 10-fold cross-validation. Accuracy (AC), balanced accuracy (BAC), sensitivity, specificity, positive predictive value, negative predictive value, and F1 score were utilized for performance assessment. RESULTS: AC, BAC, sensitivity, specificity, positive predictive value, negative predictive value, and F1 scores from the XGboost model were 98.1, 97.1, 100, 94.1, 97.2, 100, and 98.6%, respectively. According to the variable importance values from the XGboost, the HAO2, TOMM20, GPC3, and PSMB4 genes can be considered potential biomarkers for HCV-related HCC. CONCLUSION: A machine learning-based prediction method discovered genes that potentially serve as biomarkers for HCV-related HCC. After clinical confirmation of the acquired genes in the following medical study, their therapeutic use can be established. Additionally, more detailed clinical works are needed to substantiate the significant conclusions in the current study. Lippincott Williams & Wilkins 2023-09-07 /pmc/articles/PMC10553079/ /pubmed/37811067 http://dx.doi.org/10.1097/MS9.0000000000001210 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 (https://creativecommons.org/licenses/by-nc-sa/4.0/) License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/)
spellingShingle Original Research
Colak, Cemil
Kucukakcali, Zeynep
Akbulut, Sami
Artificial intelligence-based prediction of molecular and genetic markers for hepatitis C–related hepatocellular carcinoma
title Artificial intelligence-based prediction of molecular and genetic markers for hepatitis C–related hepatocellular carcinoma
title_full Artificial intelligence-based prediction of molecular and genetic markers for hepatitis C–related hepatocellular carcinoma
title_fullStr Artificial intelligence-based prediction of molecular and genetic markers for hepatitis C–related hepatocellular carcinoma
title_full_unstemmed Artificial intelligence-based prediction of molecular and genetic markers for hepatitis C–related hepatocellular carcinoma
title_short Artificial intelligence-based prediction of molecular and genetic markers for hepatitis C–related hepatocellular carcinoma
title_sort artificial intelligence-based prediction of molecular and genetic markers for hepatitis c–related hepatocellular carcinoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553079/
https://www.ncbi.nlm.nih.gov/pubmed/37811067
http://dx.doi.org/10.1097/MS9.0000000000001210
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