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Authors Yu T, Wang X, Zhu G, Han C, Su H, Liao X, Yang C, Qin W, Huang K, Peng T
Received 9 December 2017
Accepted for publication 25 March 2018
Published 25 June 2018 Volume 2018:10 Pages 1713—1726
DOI https://doi.org/10.2147/CMAR.S159425
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Amy Norman
Peer reviewer comments 4
Editor who approved publication: Dr Antonella D'Anneo
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.
Keywords: mRNA expression, CYP3A subfamily, hepatocellular carcinoma, prognosis,
biomarker