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Insight into the mitochondrial unfolded protein response and cancer: opportunities and challenges

期刊

CELL AND BIOSCIENCE
卷 12, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13578-022-00747-0

关键词

Mitochondrial unfolded protein response; Cancer; Proteostasis; Mitochondrial heat shock protein; Mitochondrial protease

资金

  1. One Hundred Person Project of Hebei Province [E2016100019]
  2. China Postdoctoral Science Foundation [2017M621099]
  3. Natural Science Foundation of Hebei Province [C2020205003]

向作者/读者索取更多资源

The mitochondrial unfolded protein response (UPRmt) is a protective transcriptional response that maintains mitochondrial proteostasis. It is regulated by similar and different factors in C. elegans and mammals. Cancer cells hijack UPRmt to promote mitochondrial repair and tumor growth. Targeting UPRmt to disrupt proteostasis in cancer cells represents a novel anticancer therapeutic strategy.
The mitochondrial unfolded protein response (UPRmt) is an evolutionarily conserved protective transcriptional response that maintains mitochondrial proteostasis by inducing the expression of mitochondrial chaperones and proteases in response to various stresses. The UPRmt-mediated transcriptional program requires the participation of various upstream signaling pathways and molecules. The factors regulating the UPRmt in Caenorhabditis elegans (C. elegans) and mammals are both similar and different. Cancer cells, as malignant cells with uncontrolled proliferation, are exposed to various challenges from endogenous and exogenous stresses. Therefore, in cancer cells, the UPRmt is hijacked and exploited for the repair of mitochondria and the promotion of tumor growth, invasion and metastasis. In this review, we systematically introduce the inducers of UPRmt, the biological processes in which UPRmt participates, the mechanisms regulating the UPRmt in C. elegans and mammals, cross-tissue signal transduction of the UPRmt and the roles of the UPRmt in promoting cancer initiation and progression. Disrupting proteostasis in cancer cells by targeting UPRmt constitutes a novel anticancer therapeutic strategy.

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