An Alternatively Spliced Variant of METTL3 Mediates Tumor Suppression in Hepatocellular Carcinoma

• Published in: Genes 2022-04, Vol.13 (4), p.669
• Main Authors: Xu, Rui-Yao, Ding, Zhan, Zhao, Qing, Ke, Tiao-Ying, Chen, Shu, Wang, Xing-Yu, Wang, Yao-Yun, Sheng, Meng-Fei, Wang, Wei, Long, Ni, Shen, Yu-Xian, Xu, Yong-Zhen, Shao, Wei
• Format: Article
• Language: English
• Subjects: Adenosine; Adenosine - genetics; Adenosine - metabolism; Alternative splicing; Antibodies; Biotechnology; Carcinoma, Hepatocellular - pathology; Cell cycle; Cell proliferation; Circadian rhythm; Gene expression; Hepatocellular carcinoma; Humans; Liver cancer; Liver Neoplasms - pathology; Malignancy; Mammals; Medical prognosis; Metabolism; Methyltransferase; Methyltransferases - genetics; Methyltransferases - metabolism; mRNA processing; N6-methyladenosine; Patients; Plasmids; Post-transcription; Proteins; RNA, Messenger - genetics; Stem cells; Transcriptomics; Tumor cell lines; Tumor suppressor genes; Tumorigenesis; Western blotting
• ISSN: 2073-4425; 2073-4425
• DOI: 10.3390/genes13040669

Many post-transcriptional mRNA processing steps play crucial roles in tumorigenesis and the progression of cancers, such as N6-methyladenosine (m A) modification and alternative splicing. Upregulation of methyltransferase-like 3 (METTL3), the catalytic core of the m A methyltransferase complex, increases m A levels and results in significant effects on the progression of hepatocellular carcinoma (HCC). However, alternative splicing of METTL3 has not been fully investigated, and the functions of its splice variants remain unclear. Here, we analyzed both our and online transcriptomic data, obtaining 13 splice variants of METTL3 in addition to canonical full-length METTL3-A in HCC cell lines and tissues. Validated by RT-qPCR and Western blotting, we found that METTL3-D, one of the splice variants expressing a truncated METTL3 protein, exhibits higher levels than METTL3-A in normal human livers but lower levels than METTL3-A in HCC tumor tissues and cell lines. Further functional assays demonstrated that METTL3-D expression decreased cellular m A modification, inhibited the proliferation, migration, and invasion of HCC cells, and was negatively associated with the malignancy of patient tumors, exhibiting functions opposite to those of full-length METTL3-A. This study demonstrates that the METTL3-D splice variant is a tumor suppressor that could potentially be used as a target for HCC therapy.