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钙信号的新前沿:化疗的一个可能靶点。

Novel frontiers in calcium signaling: A possible target for chemotherapy.

机构信息

Department of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, Laboratory for Technologies of Advanced Therapies (LTTA), University of Ferrara, Ferrara, Italy.

Department of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, Laboratory for Technologies of Advanced Therapies (LTTA), University of Ferrara, Ferrara, Italy.

出版信息

Pharmacol Res. 2015 Sep;99:82-5. doi: 10.1016/j.phrs.2015.05.008. Epub 2015 May 29.

Abstract

Intracellular calcium (Ca(2+)) is largely known as a second messenger that is able to drive effects ranging from vesicle formation to muscle contraction, energy production and much more. In spite of its physiological regulation, Ca(2+) is a strategic tool for regulating apoptosis, especially during transmission between the endoplasmic reticulum and the mitochondria. Contact sites between these organelles are well-defined as signaling platforms where oncogenes and oncosuppressors can exert anti/pro-apoptotic activities. Recent advances from in vivo investigations into these regions highlight the role of the master oncosuppressor p53 in regulating Ca(2+) transmission and apoptosis, and we propose that Ca(2+) signals are relevant targets when developing new therapeutic approaches.

摘要

细胞内钙(Ca(2+))作为一种第二信使,能够驱动从囊泡形成到肌肉收缩、能量产生等多种效应,这是广为人知的。尽管 Ca(2+)受到生理调节,但它是调节细胞凋亡的一种重要工具,尤其是在内质网和线粒体之间的传递过程中。这些细胞器之间的接触部位被明确定义为信号平台,癌基因和抑癌基因可以在此发挥抗/促凋亡作用。从体内研究这些区域的最新进展中可以看出,主抑癌基因 p53 在调节 Ca(2+)传递和细胞凋亡方面发挥着重要作用,我们提出 Ca(2+)信号是开发新治疗方法的相关靶点。

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