m6A modification–mediated lncRNA TP53TG1 inhibits gastric cancer progression by regulating CIP2A stability

Long noncoding RNAs (lncRNAs) are associated with various types of cancer. However, the precise roles of many lncRNAs in tumor progression remain unclear. In this study, we found that the expression of the lncRNA TP53TG1 was downregulated in gastric cancer (GC) and it functioned as a tumor suppresso...

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Published inCancer science Vol. 113; no. 12; pp. 4135 - 4150
Main Authors Fang, Deliang, Ou, Xinde, Sun, Kaiyu, Zhou, Xingyu, Li, Youpei, Shi, Peng, Zhao, Zirui, He, Yulong, Peng, Jianjun, Xu, Jianbo
Format Journal Article
LanguageEnglish
Published England John Wiley & Sons, Inc 01.12.2022
John Wiley and Sons Inc
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Summary:Long noncoding RNAs (lncRNAs) are associated with various types of cancer. However, the precise roles of many lncRNAs in tumor progression remain unclear. In this study, we found that the expression of the lncRNA TP53TG1 was downregulated in gastric cancer (GC) and it functioned as a tumor suppressor. In addition, low TP53TG1 expression was significantly associated with poor survival in patients with GC. TP53TG1 inhibited the proliferation, metastasis, and cell cycle progression of GC cells, while it promoted their apoptosis. m6A modification sites are highly abundant on TP53TG1, and demethylase ALKBH5 reduces TP53TG1 stability and downregulates its expression. TP53TG1 interacts with cancerous inhibitor of protein phosphatase 2A (CIP2A) and triggers its ubiquitination‐mediated degradation, resulting in the inhibition of the PI3K/AKT pathway. These results suggest that TP53TG1 plays an important role in inhibiting the progression of GC and provides a crucial target for GC treatment. Reveal the important role of TP53TG1 as a tumor suppressor in inhibiting the progression of gastric cancer (GC). Explore the specific mechanism by which TP53TG1 binds to CIP2A and promotes its ubiquitination, thus inhibiting the activation of the PI3K/AKT pathway. Discover the new mechanism of TP53TG1 downregulation mediated by m6A methylation modification in GC.
Bibliography:Deliang Fang, Xinde Ou, and Kaiyu Sun have contributed equally to this work and share first authorship.
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ISSN:1347-9032
1349-7006
1349-7006
DOI:10.1111/cas.15581