4.7 Review

Naturally derived indole alkaloids targeting regulated cell death (RCD) for cancer therapy: from molecular mechanisms to potential therapeutic targets

期刊

JOURNAL OF HEMATOLOGY & ONCOLOGY
卷 15, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13045-022-01350-z

关键词

Cancer; Indole alkaloids; Regulated cell death (RCD); Apoptosis; Autophagy; Ferroptosis; Mitotic catastrophe; Necroptosis; Anoikis; Target therapy

资金

  1. National Natural Science Foundation of China [82073998, 22001024, 82104376]
  2. Science and Technology Department of Sichuan Province [2022JDRC0045, 2021YJ0402, 2022JDRC0125]
  3. Innovation Team and Talents Cultivation Program of National Administration of Traditional Chinese Medicine [ZYYCXTD-D-202209]
  4. Xinglin Scholar Research Promotion Project of Chengdu University of TCM

向作者/读者索取更多资源

This review systematically summarizes the anticancer effects of indole alkaloids by targeting different regulated cell death (RCD) subroutines, and discusses the cross talk between different subroutines mediated by indole alkaloids and the combined strategies. The information provided in this review is important for the design of novel molecules and the development of new strategies for cancer therapy.
Regulated cell death (RCD) is a critical and active process that is controlled by specific signal transduction pathways and can be regulated by genetic signals or drug interventions. Meanwhile, RCD is closely related to the occurrence and therapy of multiple human cancers. Generally, RCD subroutines are the key signals of tumorigenesis, which are contributed to our better understanding of cancer pathogenesis and therapeutics. Indole alkaloids derived from natural sources are well defined for their outstanding biological and pharmacological properties, like vincristine, vinblastine, staurosporine, indirubin, and 3,3'-diindolylmethane, which are currently used in the clinic or under clinical assessment. Moreover, such compounds play a significant role in discovering novel anticancer agents. Thus, here we systemically summarized recent advances in indole alkaloids as anticancer agents by targeting different RCD subroutines, including the classical apoptosis and autophagic cell death signaling pathways as well as the crucial signaling pathways of other RCD subroutines, such as ferroptosis, mitotic catastrophe, necroptosis, and anoikis, in cancer. Moreover, we further discussed the cross talk between different RCD subroutines mediated by indole alkaloids and the combined strategies of multiple agents (e.g., 3,10-dibromofascaplysin combined with olaparib) to exhibit therapeutic potential against various cancers by regulating RCD subroutines. In short, the information provided in this review on the regulation of cell death by indole alkaloids against different targets is expected to be beneficial for the design of novel molecules with greater targeting and biological properties, thereby facilitating the development of new strategies for cancer therapy.

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