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致癌受体酪氨酸激酶激活的 Akt-RSK-S6 激酶信号网络。

Akt-RSK-S6 kinase signaling networks activated by oncogenic receptor tyrosine kinases.

机构信息

Cell Signaling Technology Inc., Danvers, MA 01923, USA.

出版信息

Sci Signal. 2010 Aug 24;3(136):ra64. doi: 10.1126/scisignal.2000998.

Abstract

Receptor tyrosine kinases (RTKs) activate pathways mediated by serine-threonine kinases, such as the PI3K (phosphatidylinositol 3-kinase)-Akt pathway, the Ras-MAPK (mitogen-activated protein kinase)-RSK (ribosomal S6 kinase) pathway, and the mTOR (mammalian target of rapamycin)-p70 S6 pathway, that control important aspects of cell growth, proliferation, and survival. The Akt, RSK, and p70 S6 family of protein kinases transmits signals by phosphorylating substrates on an RxRxxS/T motif (R, arginine; S, serine; T, threonine; and x, any amino acid). We developed a large-scale proteomic approach to identify more than 300 substrates of this kinase family in cancer cell lines driven by the c-Met, epidermal growth factor receptor (EGFR), or platelet-derived growth factor receptor alpha (PDGFRalpha) RTKs. We identified a subset of proteins with RxRxxS/T sites for which phosphorylation was decreased by RTK inhibitors (RTKIs), as well as by inhibitors of the PI3K, mTOR, and MAPK pathways, and we determined the effects of small interfering RNA directed against these substrates on cell viability. Phosphorylation of the protein chaperone SGTA (small glutamine-rich tetratricopeptide repeat-containing protein alpha) at serine-305 was essential for PDGFRalpha stabilization and cell survival in PDGFRalpha-dependent cancer cells. Our approach provides a new view of RTK and Akt-RSK-S6 kinase signaling, revealing previously unidentified Akt-RSK-S6 kinase substrates that merit further consideration as targets for combination therapy with RTKIs.

摘要

受体酪氨酸激酶(RTKs)激活丝氨酸-苏氨酸激酶介导的途径,如 PI3K(磷脂酰肌醇 3-激酶)-Akt 途径、Ras-MAPK(丝裂原活化蛋白激酶)-RSK(核糖体 S6 激酶)途径和 mTOR(雷帕霉素哺乳动物靶标)-p70 S6 途径,这些途径控制细胞生长、增殖和存活的重要方面。Akt、RSK 和 p70 S6 家族蛋白激酶通过磷酸化 RxRxxS/T 基序(R,精氨酸;S,丝氨酸;T,苏氨酸;和 x,任何氨基酸)上的底物来传递信号。我们开发了一种大规模蛋白质组学方法,在 c-Met、表皮生长因子受体(EGFR)或血小板衍生生长因子受体 alpha(PDGFRalpha)RTKs 驱动的癌细胞系中鉴定了该激酶家族的 300 多种底物。我们确定了一组具有 RxRxxS/T 位点的蛋白质亚基,这些蛋白质的磷酸化被 RTK 抑制剂(RTKIs)以及 PI3K、mTOR 和 MAPK 途径抑制剂降低,我们确定了针对这些底物的小干扰 RNA 的影响对细胞活力的影响。蛋白伴侣 SGTA(小谷氨酰胺富含四肽重复蛋白 alpha)在丝氨酸-305 上的磷酸化对于 PDGFRalpha 在 PDGFRalpha 依赖性癌细胞中的稳定和细胞存活至关重要。我们的方法提供了 RTK 和 Akt-RSK-S6 激酶信号的新视角,揭示了先前未被识别的 Akt-RSK-S6 激酶底物,这些底物值得进一步考虑作为与 RTKIs 联合治疗的靶标。

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本文引用的文献

1
Principles of cancer therapy: oncogene and non-oncogene addiction.
Cell. 2009 Mar 6;136(5):823-37. doi: 10.1016/j.cell.2009.02.024.
2
Deregulated EGFR signaling during lung cancer progression: mutations, amplicons, and autocrine loops.
Cancer Prev Res (Phila). 2008 Aug;1(3):156-60. doi: 10.1158/1940-6207.CAPR-08-0080.
4
Decision tree-driven tandem mass spectrometry for shotgun proteomics.
Nat Methods. 2008 Nov;5(11):959-64. doi: 10.1038/nmeth.1260. Epub 2008 Oct 19.
5
The RSK family of kinases: emerging roles in cellular signalling.
Nat Rev Mol Cell Biol. 2008 Oct;9(10):747-58. doi: 10.1038/nrm2509.
6
The impact of peptide abundance and dynamic range on stable-isotope-based quantitative proteomic analyses.
J Proteome Res. 2008 Nov;7(11):4756-65. doi: 10.1021/pr800333e. Epub 2008 Sep 18.
7
PI3K pathway alterations in cancer: variations on a theme.
Oncogene. 2008 Sep 18;27(41):5497-510. doi: 10.1038/onc.2008.245.
9
Signaling networks assembled by oncogenic EGFR and c-Met.
Proc Natl Acad Sci U S A. 2008 Jan 15;105(2):692-7. doi: 10.1073/pnas.0707270105. Epub 2008 Jan 7.
10
Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer.
Cell. 2007 Dec 14;131(6):1190-203. doi: 10.1016/j.cell.2007.11.025.

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