4.7 Article

Loss of TRIM31 promotes breast cancer progression through regulating K48-and K63-linked ubiquitination of p53

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CELL DEATH & DISEASE
卷 12, 期 10, 页码 -

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SPRINGERNATURE
DOI: 10.1038/s41419-021-04208-3

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资金

  1. National Natural Science Foundation of China (National Science Foundation of China) [81773756, 81874071, 81874071, 81773756, 82072933, 81874071, 81874071, 82072933, 81773756, 81874071, 81773756, 81874071, 81773756, 81874071, 82072933, 81773756, 82072933, 81874071, 81773756, 81874071, 81773756, 81874071, 81773756, 82072933, 82072933] Funding Source: Medline
  2. Department of Science and Technology of Sichuan Province (Sichuan Provincial Department of Science and Technology) [2017SZ0060, 2017SZ0060, 2017SZ0060, 2017SZ0060, 2017SZ0060, 2017SZ0060, 2017SZ0060, 2017SZ0060, 2017SZ0060, 2017SZ0060, 2017SZ0060] Funding Source: Medline

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TRIM31 functions as a tumor suppressor in breast cancer by stabilizing and activating p53, inhibiting the proliferation and metastasis of breast cancer cells. The interaction between TRIM31 and p53 plays a critical role in regulating p53 ubiquitination, suggesting a promising therapeutic strategy for treating breast cancer by restoring TRIM31 expression.
Breast cancer is the most common cancer in the world. Relapse and metastasis are important factors endangering the life of breast cancer patients, but the mechanism is still unclear. The stabilization of p53 is essential for preventing carcinogenesis, and ubiquitination is one of the main ways to regulate the stability of p53. Tripartite motif-containing 31 (TRIM31) is a new member of the TRIM family and functions as an E3 ubiquitin ligase. It acts as a cancer promoter or suppressor in the malignant processes of multiple cancers. However, the function of TRIM31 in breast cancer progression remains unknown. In this study, we showed that TRIM31 is downregulated in breast cancer tissues and negatively correlated with breast cancer progression. Both gain- and loss-of-function assays indicated that TRIM31 inhibits the proliferation, colony formation, migration, and invasion of breast cancer cells. Further investigation demonstrated that TRIM31 directly interacts with p53, and inducing the K63-linked ubiquitination of p53 via its RING domain, Meanwhile, TRIM31 suppresses the MDM2-mediated K48-linked ubiquitination of p53 through competitive inhibiting the interaction of MDM2 and p53, leading to the p53 stabilization and activation. Knockdown of p53 reversed the inhibitory effects of TRIM31 on the growth and metastasis of breast cancer cells. Moreover, we found that the RING and coiled-coil (C-C) domains of TRIM31 were essential for its tumor suppressor function. Taken together, our findings reveal a novel mechanism by which TRIM31 suppresses breast cancer development through the stabilization and activation of p53 and define a promising therapeutic strategy for restoring TRIM31 to treat breast cancer.

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