Dysregulated microRNAs as a biomarker for diagnosis and prognosis of hepatitis B virus-associated hepatocellular carcinoma.

World J Gastroenterol

State Key Laboratory of Virology, Department of Medical Microbiology, School of Basic Medical Sciences, Wuhan University, Wuhan 430071, Hubei Province, China.

Published: August 2023

AI Article Synopsis

  • Hepatocellular carcinoma (HCC) is a deadly cancer, and hepatitis B virus (HBV) is a major risk factor for its development.
  • Early detection of HBV-associated HCC can improve patient outcomes, and biomarkers like microRNAs (miRNAs) are crucial for diagnosis and therapy.
  • This review discusses how HBV influences miRNA expression and their role in diagnosing and treating HBV-HCC, highlighting the potential for miRNA-based applications in clinical practice.

Article Abstract

Hepatocellular carcinoma (HCC) is a malignancy with a high incidence and fatality rate worldwide. Hepatitis B virus (HBV) infection is one of the most important risk factors for its occurrence and development. Early detection of HBV-associated HCC (HBV-HCC) can improve clinical decision-making and patient outcomes. Biomarkers are extremely helpful, not only for early diagnosis, but also for the development of therapeutics. MicroRNAs (miRNAs), a subset of non-coding RNAs approximately 22 nucleotides in length, have increasingly attracted scientists' attention due to their potential utility as biomarkers for cancer detection and therapy. HBV profoundly impacts the expression of miRNAs potentially involved in the development of hepatocarcinogenesis. In this review, we summarize the current progress on the role of miRNAs in the diagnosis and treatment of HBV-HCC. From a molecular standpoint, we discuss the mechanism by which HBV regulates miRNAs and investigate the exact effect of miRNAs on the promotion of HCC. In the near future, miRNA-based diagnostic, prognostic, and therapeutic applications will make their way into the clinical routine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473924PMC
http://dx.doi.org/10.3748/wjg.v29.i31.4706DOI Listing

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