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Keyword
- cancer biology1
- cDNA1
- CDS1
- coding sequence1
- complementary DNA1
- epithelial-mesenchymal transition1
- gene expression1
- HA1
- hemagglutinin1
- IgG1
- immunoglobulin G1
- m6A1
- m6A reader protein1
- m6A RNA immunoprecipitation1
- m6A RNA-IP1
- METTL1
- mRNA stability1
- N6-methyladenosine1
- QRT-PCR1
- RIP1
- RNA immunoprecipitation1
- RNA methylation1
- TF1
- TGF-β1
Gene Regulation
1 Results
- Research ArticleOpen Access
m6A RNA methylation regulates the transcription factors JUN and JUNB in TGF-β-induced epithelial–mesenchymal transition of lung cancer cells
Journal of Biological ChemistryVol. 298Issue 11102554Published online: September 29, 2022- Kusuma Suphakhong
- Minoru Terashima
- Sasithorn Wanna-udom
- Risa Takatsuka
- Akihiko Ishimura
- Takahisa Takino
- and others
Cited in Scopus: 1N6-methyladenosine (m6A) is the most common internal chemical modification of mRNAs involved in many pathological processes including various cancers. In this study, we investigated the m6A-dependent regulation of JUN and JUNB transcription factors (TFs) during transforming growth factor-beta–induced epithelial–mesenchymal transition (EMT) of A549 and LC2/ad lung cancer cell lines, as the function and regulation of these TFs within this process remains to be clarified. We found that JUN and JUNB played an important and nonredundant role in the EMT-inducing gene expression program by regulating different mesenchymal genes and that their expressions were controlled by methyltransferase-like 3 (METTL3) m6A methyltransferase.