Background/aim: N6-Methyladenosine (m6A), the most abundant internal modification of RNA, plays a critical role in cancer development. However, the clinical implications of mA in hepatocellular carcinoma (HCC) remain unclear.
Materials And Methods: We analyzed 177 HCC and paired noncancerous liver tissues from patients who underwent hepatectomy according to global mA quantification and expression of mA demethylases fat mass and obesity-associated protein (FTO) and alpha-ketoglutarate-dependent dioxygenase alkB homolog 5 (ALKBH5).
Results: The global mA quantification revealed no significant difference between HCC and non-cancerous tissue. The expression of mA demethylases FTO and ALKBH5, was significantly lower in HCC than in non-cancerous tissues (both p<0.001). Furthermore, low ALKBH5 expression in non-cancerous tissues was significantly correlated with worse recurrence-free survival (median of 16.3 vs. 38.9 months, p=0.001).
Conclusion: mA in HCC and its demethylase in surrounding non-cancerous liver tissues might be involved in inherent mechanisms for HCC development and affect malignant potential after HCC resection.
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http://dx.doi.org/10.21873/anticanres.14690 | DOI Listing |
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