miR-539 activates the SAPK/JNK signaling pathway to promote ferropotosis in colorectal cancer by directly targeting TIPE

Colorectal cancer (CRC) is a common tumor that harms human health with a high recurrence rate. It has been reported that the expression of microRNA-539 (miR-539) is low in several types of cancer, including CRC. Tumor necrosis factor (TNF)-α-induced protein 8 (TNFAIP8/TIPE) is highly expressed in CR...

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Veröffentlicht in:Cell death discovery 2021-10, Vol.7 (1), p.272-272, Article 272
Hauptverfasser: Yang, Yan, Lin, Zeyang, Han, Zhaopu, Wu, Zhengxin, Hua, Jianyu, Zhong, Rui, Zhao, Ruidan, Ran, Honggang, Qu, Kaiyong, Huang, Hongfei, Tang, Huamei, Huang, Jiyi, Liu, Zhongchen, Hong, Xuehui, Peng, Zhihai, Zhuang, Guohong
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Sprache:eng
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Zusammenfassung:Colorectal cancer (CRC) is a common tumor that harms human health with a high recurrence rate. It has been reported that the expression of microRNA-539 (miR-539) is low in several types of cancer, including CRC. Tumor necrosis factor (TNF)-α-induced protein 8 (TNFAIP8/TIPE) is highly expressed in CRC and promotes the proliferation, migration and angiogenesis of CRC. However, the relationship between miR-539 and TIPE and the mechanisms by which they regulate the proliferation of CRC remain to be explored. We aimed to investigate the functions and mechanisms of miR-539 in CRC proliferation. Functionally, miR-539 can bind to and regulate the expression of TIPE, and miR-539 activates SAPK/JNK to downregulate the expression of glutathione peroxidase 4 (GPX4) and promote ferroptosis. Our data reveal the novel role of miR-539 in regulating ferroptosis in CRC via activation of the SAPK/JNK axis, providing new insight into the mechanism of abnormal proliferation in CRC and a novel potential therapeutic target for advanced CRC.
ISSN:2058-7716
2058-7716
DOI:10.1038/s41420-021-00659-x