MiR-203 and Endocan as Diagnostic Markers for Hepatocellular Carcinoma Related Viral Infections

Elkady, Nooran M; El-maadawy, Eman A; GadAllah, Mahmoud; Elmalawany, Alshimaa M; Elshal, Mohamed F

doi:10.21608/ajbs.2024.253715.1064

MiR-203 and Endocan as Diagnostic Markers for Hepatocellular Carcinoma Related Viral Infections

Document Type : Original Article

Authors

¹ Molecular Biology Department, Genetic Engineering and Biotechnology Research Institute [GEBRI], University of Sadat City, Egypt

² Molecular Biology Department, Genetic Engineering and Biotechnology Research Institute [GEBRI], University of Sadat City, Egypt. Postal code 32897

³ Molecular Diagnostics Department, Genetic Engineering and Biotechnology Research Institute [GEBRI], University of Sadat City, Egypt

⁴ Department of Clinical Pathology, National Liver Institute, Menoufia University, Egypt.

10.21608/ajbs.2024.253715.1064

Abstract

Purpose: We aimed to evaluate the expression of miR-203 and serum endocan in Hepatocellular carcinoma (HCC) patients suffered from hepatitis C virus (HCV) or hepatitis B virus (HBV) to investigate their diagnostic value.

Subjects and methods: This case control study was conducted on 70 patients divided into 29 HCC [20 on top of HCV and 9 on top of HBV], non-HCC chronic liver disease [20 positive HCV and 21 positive HBV] patients. Ten healthy volunteers were recruited as controls. The expression of miR-203 was detected using quantitative real time (qRT-PCR). Serum endocan was assessed by Enzyme linked immunosorbent assay (ELISA).

Results: A significant reduction was detected in miR-203 expression level in HCC-related HCV group compared to HCV (p<0.001) and control group (p<0.001) and in HCV group compared to controls (p<0.001). Interestingly, miR-203 was significantly increased (p<0.001) in HCC-related HBV group compared to HCC-related HCV group. With a significant elevation (p<0.01) in HBV versus HCV group. At a cutoff value of 0.3276, miR-203 showed 100% sensitivity and 90% specificity [AUC=0.989] in HCC-related HCV group. Serum Endocan was significantly elevated (p<0.05] in HCC patients versus controls. A significant increase (p<0.05] was found in HCC-related HCV compared to HCV group, with a significant diminution (p<0.001) in HBV group versus controls. HCV patients showed a significant increase (p<0.05] in endocan level compared to HBV ones.

Conclusion: miR-203 and serum endocan could be used as diagnostic markers for HCC related different viral infection in Egyptian patients. Further research is required to confirm our findings.

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