Targeting m7G-enriched circKDM1A prevents colorectal cancer progression

Plenty of circRNAs have been reported to play an important role in colorectal cancer (CRC), while the reason of abnormal circRNA expression in cancer still keep elusive. Here, we found that m7G RNA modifications were enriched in some circRNAs, these m7G modifications in circRNAs were catalyzed by METTL1, and the GG motif was the main site preference for m7G modifications in circRNAs. We further confirmed that METTL1 played a cancer-promoting role in CRC. We then screened a highly expressed circRNA, called circKDM1A, and found that METTL1 prevented the degradation of circKDM1A by m7G modification. CircKDM1A was further verified to promote proliferation, invasion and migration of CRC in vivo and in vitro. Its cancer-promoting ability was weakened after the m7G site mutation. CircKDM1A was verified to activate AKT pathway by upregulating PDK1, consequently promoting CRC progression. These results suggest that m7G-modified circRNA promotes CRC progression via activating AKT pathway. Our study uncovers an essential physiological function and mechanism of METTL1-mediated m7G modification in the regulation of circRNA stability and cancer progression.

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Publication Details

Journal
Molecular Cancer
Published
2024-08-30
DOI
https://doi.org/10.1186/s12943-024-02090-z
Citations
23
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
5.38

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article

Targeting m7G-enriched circKDM1A prevents colorectal cancer progression

Chaohua Si, Chengzeng Wang, Yanxin Xu, Yaxin Guo et al.
23 citations
Molecular Cancer
RNA modifications and cancer
5.38
article

Targeting m7G-enriched circKDM1A prevents colorectal cancer progression

Chaohua Si, Chengzeng Wang, Yanxin Xu, Yaxin Guo, Chen Chen, Zhenqiang Sun, Xiaoke Wu
article en
23 citations

Abstract

Plenty of circRNAs have been reported to play an important role in colorectal cancer (CRC), while the reason of abnormal circRNA expression in cancer still keep elusive. Here, we found that m7G RNA modifications were enriched in some circRNAs, these m7G modifications in circRNAs were catalyzed by METTL1, and the GG motif was the main site preference for m7G modifications in circRNAs. We further confirmed that METTL1 played a cancer-promoting role in CRC. We then screened a highly expressed circRNA, called circKDM1A, and found that METTL1 prevented the degradation of circKDM1A by m7G modification. CircKDM1A was further verified to promote proliferation, invasion and migration of CRC in vivo and in vitro. Its cancer-promoting ability was weakened after the m7G site mutation. CircKDM1A was verified to activate AKT pathway by upregulating PDK1, consequently promoting CRC progression. These results suggest that m7G-modified circRNA promotes CRC progression via activating AKT pathway. Our study uncovers an essential physiological function and mechanism of METTL1-mediated m7G modification in the regulation of circRNA stability and cancer progression.

Molecular CancerVol. 23(1)
Zhengzhou University (CN), First Affiliated Hospital of Henan University (CN), First Affiliated Hospital of Zhengzhou University (CN)
National Natural Science Foundation of China
Good health and well-being
Openalex Percentile: Top 3%
RNA modifications and cancer
5.38
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