Published online Oct 15, 2025. doi: 10.4251/wjgo.v17.i10.106692
Revised: April 4, 2025
Accepted: April 21, 2025
Published online: October 15, 2025
Processing time: 223 Days and 16.1 Hours
This article discusses the recently published study by Ji et al on the role of MEX3A in hepatocellular carcinoma. The study reveals MEX3A’s role, but has issues including a small sample size and unclear RORA-regulation. We propose new research directions. It is essential to analyze the immune cells in MEX3A-high tumors and test the impact of MEX3A-knockout on immunotherapy when exploring the relationship between MEX3A and the immune microenvironment. With regard to MEX3A and cancer stem cells, it is necessary to assess the effect of MEX3A on cancer stem cell self-renewal and use organoids to test the targeting ability of MEX3A-inhibitors. In addition, improvements such as larger-scale validation and in-depth mechanism research are required, which could boost hepatocellular carcinoma understanding and patient prognosis.
Core Tip: The study by Ji et al explored MEX3A’s role in hepatocellular carcinoma, and showed its potential as a marker and target. However, the study has limitations such as a small sample size. New directions include studying its relationship with the immune microenvironment and cancer stem cells, such as analyzing the composition of immune cells and detecting the effect of knockdown of MEX3A on immunotherapy. Addressing these issues may improve hepatocellular carcinoma prognosis.
