Cell Death Discovery (Oct 2021)

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

  • Yan Yang,
  • Zeyang Lin,
  • Zhaopu Han,
  • Zhengxin Wu,
  • Jianyu Hua,
  • Rui Zhong,
  • Ruidan Zhao,
  • Honggang Ran,
  • Kaiyong Qu,
  • Hongfei Huang,
  • Huamei Tang,
  • Jiyi Huang,
  • Zhongchen Liu,
  • Xuehui Hong,
  • Zhihai Peng,
  • Guohong Zhuang

DOI
https://doi.org/10.1038/s41420-021-00659-x
Journal volume & issue
Vol. 7, no. 1
pp. 1 – 9

Abstract

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Abstract 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.