AI Article Synopsis

  • Hepatocellular carcinoma (HCC) is a common and deadly cancer, and long noncoding RNAs like HOTAIR may help diagnose it.
  • In a study, researchers measured serum HOTAIR levels in patients with hepatitis, liver cirrhosis, and HCC, finding higher levels in HCC patients.
  • The results suggest that HOTAIR could be an effective diagnostic marker for HCC, especially when used alongside other clinical indicators like HBeAg and AFP, improving overall diagnostic accuracy.

Article Abstract

Background/aims:  Hepatocellular carcinoma (HCC) is one of the most common malignant tumors and the third leading cause of cancer-related mortality. Extensive literature suggests that long noncoding RNAs play a role in the progression of HCC and hold potential as diagnostic biomarkers for this disease.

Materials And Methods:  We examined the serum levels of HOX antisense intergenic RNA (HOTAIR) in 49 hepatitis patients, 31 liver cirrhosis (LC), and 37 HCC patients using quantitative real-time polymerase chain reaction. Correlations between serum HOTAIR levels and clinical data were evaluated in HCC patients. The receiver operating characteristic curve was utilized to analyze the diagnostic potency of HOTAIR.

Results:  The HOTAIR levels in serum were significantly higher in HCC patients compared to those with hepatitis (P = .003) and LC patients (P = .048). There was a significant association between the serum levels of HOTAIR and positivity of hepatitis B e antigen (HBeAg) (P = .039) as well as portal vein tumor thrombus (P = .040) in HCC patients. The area under the curve (AUC) for HOTAIR for distinguishing HCC from hepatitis and LC was 0.697. The combined AUC for HOTAIR, HBeAg, and alpha-fetoprotein (AFP) was 0.777.

Conclusion:  Serum HOTAIR functions as a potential diagnostic marker for hepatitis B virus-related HCC. Combining HOTAIR with clinical data and AFP can reinforce the diagnostic precision on HCC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11181209PMC
http://dx.doi.org/10.5152/tjg.2024.23314DOI Listing

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