METTL14 suppresses the metastatic potential of hepatocellular carcinoma by modulating N6‐methyladenosine‐dependent primary MicroRNA processing
By Jin‐zhao Ma, Fu Yang, Chuan‐chuan Zhou, Feng Liu, Ji-hang Yuan, F. Wang, Tian‐tian Wang, Qing‐guo Xu, Weiping Zhou, Shuhan Sun. Hepatology, 2017
760 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/841e8e882c24ea00079cef3b5a72be2f7fac1964
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In Cancer Research
In Molecular Biology
Citations in the corpus
- RNA N6-methyladenosine modification in cancers: current status and perspectives (2018, background): “, mir-126) processing by interaction with DGCR8.(86) In contrast, Chen et al.”
- Critical Roles of N6-Methyladenosine (m6A) in Cancer and Virus Infection (2020, background): “Another study revealed that temperature stress re-localizes METTL3 and the DGCR8 microprocessor complex subunit (DGCR8) to stress-induced genes including heat shock protein 70 (Hsp70), for further degradation [78].”
- RNA N6‐methyladenosine methyltransferase‐like 3 promotes liver cancer progression through YTHDF2‐dependent posttranscriptional silencing of SOCS2 (2018, background): “Recently, Ma et al.((38)) reported that METTL14 was suppressed in HCC and impaired primary miRNA processing to promote HCC metastasis.”
- The role of m6A RNA methylation in cancer metabolism (2022, background): “By interacting with DGCR8, METTL14 positively regulates the expression of pre-miR-126, and miR-126 also reversely inhibits the inhibitory effect of METTL14 on tumor cell metastasis [112].”
- The potential role of RNA N6-methyladenosine in Cancer progression (2020, result): “In addition, studies have reported conflicting findings in the same type of cancer; for example, in liver cancer, METTL3 and METTL14 play completely opposite roles in tumor development [105, 157].”
- Functions of N6-methyladenosine and its role in cancer (2019, background): “METTL14 not only enhances the recognition and binding of microprocessor protein DGCR8 to pri-mi126, but also promotes the subsequent processing to mature miRNA [125].”