FoxO1 promotes ovarian cancer by increasing transcription and METTL14‐mediated m6A modification of SMC4

Author:

Tan Liping12,Wang Shuangan12,Huang Shijia3,Tie Yujuan12,Sai Na12,Mao Yichen12,Zhao Shuli3,Hou Yayi12,Dou Huan12ORCID

Affiliation:

1. The State Key Laboratory of Pharmaceutical Biotechnology, Division of Immunology, Medical School Nanjing University Nanjing China

2. Jiangsu Key Laboratory of Molecular Medicine Nanjing China

3. General Clinical Research Center, Nanjing First Hospital Nanjing Medical University Nanjing China

Abstract

AbstractThe transcription factor forkhead box protein O1 (FoxO1) is closely related to the occurrence and development of ovarian cancer (OC), however its role and molecular mechanisms remain unclear. Herein, we found that FoxO1 was highly expressed in clinical samples of OC patients and was significantly correlated with poor prognosis. FoxO1 knockdown inhibited the proliferation of OC cells in vitro and in vivo. ChIP‐seq combined with GEPIA2 and Kaplan–Meier database analysis showed that structural maintenance of chromosome 4 (SMC4) is a downstream target of FoxO1, and FoxO1 promotes SMC4 transcription by binding to its −1400/−1390 bp promoter. The high expression of SMC4 significantly blocked the tumor inhibition effect of FoxO1 knockdown. Furtherly, FoxO1 increased SMC4 mRNA abundance by transcriptionally activating methyltransferase‐like 14 (METTL14) and increasing SMC4 m6A methylation on its coding sequence region. The Cancer Genome Atlas dataset analysis confirmed a significant positive correlation between FoxO1, SMC4, and METTL14 expression in OC. In summary, this study revealed the molecular mechanisms of FoxO1 regulating SMC4 and established a clinical link between the expression of FoxO1/METTL14/SMC4 in the occurrence of OC, thus providing a potential diagnostic target and therapeutic strategy.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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