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Machine learning identifies exosome features related to hepatocellular carcinoma

Background: Hepatocellular carcinoma (HCC) is one of the most malignant tumors with a poor prognosis. There is still a lack of effective biomarkers to predict its prognosis. Exosomes participate in intercellular communication and play an important role in the development and progression of cancers....

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Autores principales: Zhu, Kai, Tao, Qiqi, Yan, Jiatao, Lang, Zhichao, Li, Xinmiao, Li, Yifei, Fan, Congcong, Yu, Zhengping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527306/
https://www.ncbi.nlm.nih.gov/pubmed/36200042
http://dx.doi.org/10.3389/fcell.2022.1020415
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author Zhu, Kai
Tao, Qiqi
Yan, Jiatao
Lang, Zhichao
Li, Xinmiao
Li, Yifei
Fan, Congcong
Yu, Zhengping
author_facet Zhu, Kai
Tao, Qiqi
Yan, Jiatao
Lang, Zhichao
Li, Xinmiao
Li, Yifei
Fan, Congcong
Yu, Zhengping
author_sort Zhu, Kai
collection PubMed
description Background: Hepatocellular carcinoma (HCC) is one of the most malignant tumors with a poor prognosis. There is still a lack of effective biomarkers to predict its prognosis. Exosomes participate in intercellular communication and play an important role in the development and progression of cancers. Methods: In this study, two machine learning methods (univariate feature selection and random forest (RF) algorithm) were used to select 13 exosome-related genes (ERGs) and construct an ERG signature. Based on the ERG signature score and ERG signature-related pathway score, a novel RF signature was generated. The expression of BSG and SFN, members of 13 ERGs, was examined using real-time quantitative polymerase chain reaction and immunohistochemistry. Finally, the effects of the inhibition of BSG and SFN on cell proliferation were examined using the cell counting kit-8 (CCK-8) assays. Results: The ERG signature had a good predictive performance, and the ERG score was determined as an independent predictor of HCC overall survival. Our RF signature showed an excellent prognostic ability with the area under the curve (AUC) of 0.845 at 1 year, 0.811 at 2 years, and 0.801 at 3 years in TCGA, which was better than the ERG signature. Notably, the RF signature had a good performance in the prediction of HCC prognosis in patients with the high exosome score and high NK score. Enhanced BSG and SFN levels were found in HCC tissues compared with adjacent normal tissues. The inhibition of BSG and SFN suppressed cell proliferation in Huh7 cells. Conclusion: The RF signature can accurately predict prognosis of HCC patients and has potential clinical value.
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spelling pubmed-95273062022-10-04 Machine learning identifies exosome features related to hepatocellular carcinoma Zhu, Kai Tao, Qiqi Yan, Jiatao Lang, Zhichao Li, Xinmiao Li, Yifei Fan, Congcong Yu, Zhengping Front Cell Dev Biol Cell and Developmental Biology Background: Hepatocellular carcinoma (HCC) is one of the most malignant tumors with a poor prognosis. There is still a lack of effective biomarkers to predict its prognosis. Exosomes participate in intercellular communication and play an important role in the development and progression of cancers. Methods: In this study, two machine learning methods (univariate feature selection and random forest (RF) algorithm) were used to select 13 exosome-related genes (ERGs) and construct an ERG signature. Based on the ERG signature score and ERG signature-related pathway score, a novel RF signature was generated. The expression of BSG and SFN, members of 13 ERGs, was examined using real-time quantitative polymerase chain reaction and immunohistochemistry. Finally, the effects of the inhibition of BSG and SFN on cell proliferation were examined using the cell counting kit-8 (CCK-8) assays. Results: The ERG signature had a good predictive performance, and the ERG score was determined as an independent predictor of HCC overall survival. Our RF signature showed an excellent prognostic ability with the area under the curve (AUC) of 0.845 at 1 year, 0.811 at 2 years, and 0.801 at 3 years in TCGA, which was better than the ERG signature. Notably, the RF signature had a good performance in the prediction of HCC prognosis in patients with the high exosome score and high NK score. Enhanced BSG and SFN levels were found in HCC tissues compared with adjacent normal tissues. The inhibition of BSG and SFN suppressed cell proliferation in Huh7 cells. Conclusion: The RF signature can accurately predict prognosis of HCC patients and has potential clinical value. Frontiers Media S.A. 2022-09-19 /pmc/articles/PMC9527306/ /pubmed/36200042 http://dx.doi.org/10.3389/fcell.2022.1020415 Text en Copyright © 2022 Zhu, Tao, Yan, Lang, Li, Li, Fan and Yu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Zhu, Kai
Tao, Qiqi
Yan, Jiatao
Lang, Zhichao
Li, Xinmiao
Li, Yifei
Fan, Congcong
Yu, Zhengping
Machine learning identifies exosome features related to hepatocellular carcinoma
title Machine learning identifies exosome features related to hepatocellular carcinoma
title_full Machine learning identifies exosome features related to hepatocellular carcinoma
title_fullStr Machine learning identifies exosome features related to hepatocellular carcinoma
title_full_unstemmed Machine learning identifies exosome features related to hepatocellular carcinoma
title_short Machine learning identifies exosome features related to hepatocellular carcinoma
title_sort machine learning identifies exosome features related to hepatocellular carcinoma
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527306/
https://www.ncbi.nlm.nih.gov/pubmed/36200042
http://dx.doi.org/10.3389/fcell.2022.1020415
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