靶向锌(II)信号传导预防癌症

Silvia Ziliotto, Olivia Ogle, Kathryn M Taylor
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引用次数: 10

摘要

锌是一种重要的元素,作为癌症治疗的潜在靶点正在获得动力。近年来,锌已被认为是第二信使,现在被认为能够在细胞外刺激的几分钟内通过从细胞内储存的锌(II)释放激活许多信号通路。锌的储存释放的主要作用之一是抑制大量酪氨酸磷酸酶,这将阻止酪氨酸激酶的失活,从而促进酪氨酸激酶依赖信号通路的进一步激活。众所周知,这些信号通路中的大多数不仅参与驱动异常的癌症生长,而且通常是主要的驱动力。所有这些数据加在一起,现在将锌和锌信号定位为潜在的重要新靶点,以防止侵袭性癌症的生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting Zinc(II) Signalling to Prevent Cancer.

Zinc is an important element that is gaining momentum as a potential target for cancer therapy. In recent years zinc has been accepted as a second messenger that is now recognized to be able to activate many signalling pathways within a few minutes of an extracellular stimulus by release of zinc(II) from intracellular stores. One of the major effects of this store release of zinc is to inhibit a multitude of tyrosine phosphatases which will prevent the inactivation of tyrosine kinases and hence, encourage further activation of tyrosine kinasedependent signalling pathways. Most of these signalling pathways are not only known to be involved in driving aberrant cancer growth, they are usually the main driving force. All this data together now positions zinc and zinc signalling as potentially important new targets to prevent aggressive cancer growth.

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