miR-516a-3P, a potential circulating biomarker in hepatocellular carcinoma, correlated with rs738409 polymorphism in PNPLA3

Author:

Youssef Samar Samir1ORCID,Youness Rana Ahmed23,Abbas Eman Abd El-Razek1,Osman Noha Mohamed4,ELFiky Asmaa5,El-Kassas Mohamed6

Affiliation:

1. Microbial Biotechnology Department, National Research Centre, 33 El Buhouth St., Dokki, Cairo, 12622, Egypt

2. School of Life & Medical Sciences, University of Hertfordshire Hosted by Global Academic Foundation, New Administrative Capital, Cairo, 11578, Egypt

3. Pharmaceutical Biology Department, Faculty of Pharmacy & Biotechnology, German University in Cairo, Cairo, Egypt

4. Cell Biology Department, National Research Centre, 33 El Buhouth St., Dokki, Cairo, 12622, Egypt

5. Environmental & Occupational Medicine Department, Environmental Research Division, National Research Centre, 33 El Buhouth St., Dokki, Cairo, 12622, Egypt

6. Endemic Medicine Department, Faculty of Medicine, Helwan University, Cairo, 11795, Egypt

Abstract

Aim: The aim was to investigate the expression profile of miR-516a-3P and its correlation with the  PNPLA3 rs738409 polymorphism in Egyptian hepatitis C virus (HCV) and hepatocellular carcinoma (HCC) patients. Materials & methods: miR-516a-3P was quantified and rs738409 was genotyped by quantitative reverse transcription PCR. Results: miR-516a-3P was significantly upregulated in HCC patients compared with HCV patients (p = 0.001). Receiver operating characteristic curve analysis confirmed that miR-516a-3P discriminates HCC from HCV (p = 0.001). A significant (p = 0.015) correlation between miR-516a-3p level and PNPLA3 rs738409 genotypes was recorded in HCV patients, yet it was not recorded in either healthy individuals or HCC patients. miR-516a-3p level was significantly (p = 0.001) higher in HCV patients carrying the rs738409 GG genotype than in those carrying the CC genotype. Conclusion: miR-516a-3P is a potential biomarker in HCC. PNPLA3 rs738409 GG carriers affect miR-516a-3P expression in HCV, and this may highlight a new mechanism in liver disease.

Publisher

Future Medicine Ltd

Subject

Pharmacology,Molecular Medicine,General Medicine

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