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依赖受体:癌症治疗的新靶点。

Dependence receptors: new targets for cancer therapy.

机构信息

Department of Clinical Pathology, Victorian Comprehensive Cancer Centre, The University of Melbourne, Melbourne, Vic., Australia.

University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Vic., Australia.

出版信息

EMBO Mol Med. 2021 Nov 8;13(11):e14495. doi: 10.15252/emmm.202114495. Epub 2021 Sep 20.

Abstract

Dependence receptors are known to promote survival and positive signaling such as proliferation, migration, and differentiation when activated, but to actively trigger apoptosis when unbound to their ligand. Their abnormal regulation was shown to be an important feature of tumorigenesis, allowing cancer cells to escape apoptosis triggered by these receptors while promoting in parallel major aspects of tumorigenesis such as proliferation, angiogenesis, invasiveness, and chemoresistance. This involvement in multiple cancer hallmarks has raised interest in dependence receptors as targets for cancer therapy. Although additional studies remain necessary to fully understand the complexity of signaling pathways activated by these receptors and to target them efficiently, it is now clear that dependence receptors represent very exciting targets for future cancer treatment. This manuscript reviews current knowledge on the contribution of dependence receptors to cancer and highlights the potential for therapies that activate pro-apoptotic functions of these proteins.

摘要

依赖受体在被激活时已知能够促进存活和正向信号转导,如增殖、迁移和分化,但在未与其配体结合时会主动触发细胞凋亡。已经表明,它们的异常调节是肿瘤发生的一个重要特征,使癌细胞能够逃避这些受体触发的凋亡,同时促进肿瘤发生的主要方面,如增殖、血管生成、侵袭和化疗耐药性。这种对多种癌症特征的参与引起了人们对依赖受体作为癌症治疗靶点的兴趣。尽管还需要进一步的研究来充分了解这些受体激活的信号通路的复杂性并有效地针对它们,但现在很清楚,依赖受体代表了未来癌症治疗的非常有前途的靶点。本文综述了依赖受体对癌症的贡献,并强调了激活这些蛋白促凋亡功能的治疗方法的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5d7/8573599/da7daf7c0eb1/EMMM-13-e14495-g003.jpg

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