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细胞周期蛋白磷酸酶CDC25的作用时间和作用位置。

The when and wheres of CDC25 phosphatases.

作者信息

Boutros Rose, Dozier Christine, Ducommun Bernard

机构信息

LBCMCP-CNRS UMR5088, IFR109, Université Paul Sabatier, 118 route de Narbonne, 31062 Toulouse, France.

出版信息

Curr Opin Cell Biol. 2006 Apr;18(2):185-91. doi: 10.1016/j.ceb.2006.02.003. Epub 2006 Feb 17.

Abstract

The CDC25 phosphatases are key regulators of normal cell division and the cell's response to DNA damage. Earlier studies suggested non-overlapping roles for each isoform during a specific cell cycle phase. However, recent data suggest that multiple CDC25 isoforms cooperate to regulate each cell cycle transition. For instance, although CDC25A was initially thought to exclusively regulate the G(1)-S transition, recent data demonstrate a significant role for CDC25A in the G(2)-M transition. Further evidence demonstrates that in addition to the ATM/ATR-CHK pathway, a p38-MAPKAP pathway is also involved in controlling CDC25 activity during G(2)/M checkpoint activation. Together with the fact that CDC25 overexpression is reported in many cancers, these data highlight the significance of developing specific CDC25 inhibitors for cancer therapy.

摘要

细胞周期蛋白磷酸酶25(CDC25)是正常细胞分裂以及细胞对DNA损伤反应的关键调节因子。早期研究表明,每种亚型在特定细胞周期阶段发挥互不重叠的作用。然而,最近的数据表明,多种CDC25亚型协同调节细胞周期的每个转换过程。例如,尽管最初认为CDC25A专门调节G1期向S期的转换,但最近的数据表明CDC25A在G2期向M期的转换中也发挥着重要作用。进一步的证据表明,除了ATM/ATR-CHK途径外,p38-MAPKAP途径也参与了G2/M期检查点激活过程中对CDC25活性的控制。鉴于许多癌症中都报道有CDC25的过表达,这些数据凸显了开发特异性CDC25抑制剂用于癌症治疗的重要性。

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