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The prognostic value of differentially expressed CYP3A subfamily members for hepatocellular carcinoma

OBJECTIVE: The activities of four cytochrome P3A (CYP3A) subfamily members (CYP3A4, CYP3A5, CYP3A7, and CYP3A43) are well documented in drug metabolism. However, the association between CYP3A subfamily members and hepatocellular carcinoma (HCC) remains unclear. This study investigated the prognostic...

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Autores principales: Yu, Tingdong, Wang, Xiangkun, Zhu, Guangzhi, Han, Chuangye, Su, Hao, Liao, Xiwen, Yang, Chengkun, Qin, Wei, Huang, Ketuan, Peng, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025769/
https://www.ncbi.nlm.nih.gov/pubmed/29983591
http://dx.doi.org/10.2147/CMAR.S159425
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author Yu, Tingdong
Wang, Xiangkun
Zhu, Guangzhi
Han, Chuangye
Su, Hao
Liao, Xiwen
Yang, Chengkun
Qin, Wei
Huang, Ketuan
Peng, Tao
author_facet Yu, Tingdong
Wang, Xiangkun
Zhu, Guangzhi
Han, Chuangye
Su, Hao
Liao, Xiwen
Yang, Chengkun
Qin, Wei
Huang, Ketuan
Peng, Tao
author_sort Yu, Tingdong
collection PubMed
description OBJECTIVE: The activities of four cytochrome P3A (CYP3A) subfamily members (CYP3A4, CYP3A5, CYP3A7, and CYP3A43) are well documented in drug metabolism. However, the association between CYP3A subfamily members and hepatocellular carcinoma (HCC) remains unclear. This study investigated the prognostic value of CYP3A subfamily mRNA expression levels with HCC prognosis. MATERIALS AND METHODS: Data from a total of 360 HCC patients were retrieved from The Cancer Genome Atlas database, and data from 231 HCC patients were retrieved from the Gene Expression Omnibus database. Kaplan–Meier analysis and Cox regression models were utilized to determine median survival, overall survival, and recurrence-free survival. Hazard ratios and 95% CI were calculated. RESULTS: Low expression of CYP3A4, CYP3A5, and CYP3A43 in the tumor tissue was associated with short median survival (crude p=0.004, 0.001, and 0.001; adjusted p=0.022, 0.005, and 0.013, respectively). Joint-effects combination analysis of CYP3A4, CYP3A5/CYP3A4, CYP3A43/CYP3A5, and CYP3A43 revealed that high expression groups of two genes (group C, group c, group 3) were associated with a reduced risk of death, as compared to low expression of two genes (group A, group a, group 1), and the adjusted p values were 0.001, 0.004, and 0.001, respectively. Joint-effects analysis of CYP3A4, CYP3A5, and CYP3A43 showed that groups III and IV had a reduced risk of death, as compared to group I (adjusted p=0.024 and 0.002, respectively). CONCLUSION: CYP3A4, CYP3A5, and CYP3A43 mRNA expression levels are potential prognostic markers of HCC.
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spelling pubmed-60257692018-07-06 The prognostic value of differentially expressed CYP3A subfamily members for hepatocellular carcinoma Yu, Tingdong Wang, Xiangkun Zhu, Guangzhi Han, Chuangye Su, Hao Liao, Xiwen Yang, Chengkun Qin, Wei Huang, Ketuan Peng, Tao Cancer Manag Res Original Research OBJECTIVE: The activities of four cytochrome P3A (CYP3A) subfamily members (CYP3A4, CYP3A5, CYP3A7, and CYP3A43) are well documented in drug metabolism. However, the association between CYP3A subfamily members and hepatocellular carcinoma (HCC) remains unclear. This study investigated the prognostic value of CYP3A subfamily mRNA expression levels with HCC prognosis. MATERIALS AND METHODS: Data from a total of 360 HCC patients were retrieved from The Cancer Genome Atlas database, and data from 231 HCC patients were retrieved from the Gene Expression Omnibus database. Kaplan–Meier analysis and Cox regression models were utilized to determine median survival, overall survival, and recurrence-free survival. Hazard ratios and 95% CI were calculated. RESULTS: Low expression of CYP3A4, CYP3A5, and CYP3A43 in the tumor tissue was associated with short median survival (crude p=0.004, 0.001, and 0.001; adjusted p=0.022, 0.005, and 0.013, respectively). Joint-effects combination analysis of CYP3A4, CYP3A5/CYP3A4, CYP3A43/CYP3A5, and CYP3A43 revealed that high expression groups of two genes (group C, group c, group 3) were associated with a reduced risk of death, as compared to low expression of two genes (group A, group a, group 1), and the adjusted p values were 0.001, 0.004, and 0.001, respectively. Joint-effects analysis of CYP3A4, CYP3A5, and CYP3A43 showed that groups III and IV had a reduced risk of death, as compared to group I (adjusted p=0.024 and 0.002, respectively). CONCLUSION: CYP3A4, CYP3A5, and CYP3A43 mRNA expression levels are potential prognostic markers of HCC. Dove Medical Press 2018-06-25 /pmc/articles/PMC6025769/ /pubmed/29983591 http://dx.doi.org/10.2147/CMAR.S159425 Text en © 2018 Yu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Yu, Tingdong
Wang, Xiangkun
Zhu, Guangzhi
Han, Chuangye
Su, Hao
Liao, Xiwen
Yang, Chengkun
Qin, Wei
Huang, Ketuan
Peng, Tao
The prognostic value of differentially expressed CYP3A subfamily members for hepatocellular carcinoma
title The prognostic value of differentially expressed CYP3A subfamily members for hepatocellular carcinoma
title_full The prognostic value of differentially expressed CYP3A subfamily members for hepatocellular carcinoma
title_fullStr The prognostic value of differentially expressed CYP3A subfamily members for hepatocellular carcinoma
title_full_unstemmed The prognostic value of differentially expressed CYP3A subfamily members for hepatocellular carcinoma
title_short The prognostic value of differentially expressed CYP3A subfamily members for hepatocellular carcinoma
title_sort prognostic value of differentially expressed cyp3a subfamily members for hepatocellular carcinoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025769/
https://www.ncbi.nlm.nih.gov/pubmed/29983591
http://dx.doi.org/10.2147/CMAR.S159425
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