4.2 Review

STAT3 pathway in cancers: Past, present, and future

期刊

MEDCOMM
卷 3, 期 2, 页码 -

出版社

WILEY
DOI: 10.1002/mco2.124

关键词

cancer hallmarks; cancer treatment; STAT3 pathway inhibitors; STAT3

资金

  1. National Natural Science Foundation of China [81702703, 81872203]
  2. China Postdoctoral Science Foundation [2018M630883, 2019T120688]
  3. Hubei Province Natural Science Foundation of China [2019CFB181]
  4. Wuhan Young Medical Talents Training Project
  5. Key Research and Development Program of Science and Technology Department of Sichuan Province [2020YFS0570, 2019YFS0514]

向作者/读者索取更多资源

This review provides an overview of the history, research advances, and prospects of the STAT3 pathway in cancer. It discusses the mechanisms of STAT3 pathway regulation, the cancer hallmarks induced by this pathway, and the emerging development of inhibitors and drug delivery systems targeting STAT3. The review also addresses the barriers and promising targets in the STAT3 pathway, as well as the overall utility of STAT3 pathway inhibitors in cancer treatment.
Signal transducer and activator of transcription 3 (STAT3), a member of the STAT family, discovered in the cytoplasm of almost all types of mammalian cells, plays a significant role in biological functions. The duration of STAT3 activation in normal tissues is a transient event and is strictly regulated. However, in cancer tissues, STAT3 is activated in an aberrant manner and is induced by certain cytokines. The continuous activation of STAT3 regulates the expression of downstream proteins associated with the formation, progression, and metastasis of cancers. Thus, elucidating the mechanisms of STAT3 regulation and designing inhibitors targeting the STAT3 pathway are considered promising strategies for cancer treatment. This review aims to introduce the history, research advances, and prospects concerning the STAT3 pathway in cancer. We review the mechanisms of STAT3 pathway regulation and the consequent cancer hallmarks associated with tumor biology that are induced by the STAT3 pathway. Moreover, we summarize the emerging development of inhibitors that target the STAT3 pathway and novel drug delivery systems for delivering these inhibitors. The barriers against targeting the STAT3 pathway, the focus of future research on promising targets in the STAT3 pathway, and our perspective on the overall utility of STAT3 pathway inhibitors in cancer treatment are also discussed.

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