Suppr超能文献

只有一小部分 Met 激活途径是维持致癌基因成瘾所必需的。

Only a subset of Met-activated pathways are required to sustain oncogene addiction.

机构信息

Division of Molecular Oncology, Institute for Cancer Research and Treatment (IRCC), University of Torino Medical School, 10060 Candiolo (Torino), Italy.

出版信息

Sci Signal. 2009 Dec 8;2(100):ra80. doi: 10.1126/scisignal.2000643.

Abstract

Tumor onset and progression require the accumulation of many genetic and epigenetic lesions. In some cases, however, cancer cells rely on only one of these lesions to maintain their malignant properties, and this dependence results in tumor regression upon oncogene inactivation ("oncogene addiction"). Determining which nodes of the many networks operative in the transformed phenotype specifically mediate this response to oncogene neutralization is crucial to identifying the vulnerabilities of cancer. Using the Met receptor as the major model system, we combined multiplex phosphoproteomics, genome-wide expression profiling, and functional assays in various cancer cells addicted to oncogenic receptor tyrosine kinases. We found that Met blockade affected a limited subset of Met downstream signals: Little or no effect was observed for several pathways downstream of Met; instead, only a restricted and pathway-specific signature of transducers and transcriptional effectors downstream of Ras or phosphoinositide 3-kinase (PI3K) was inactivated. An analogous signature was also generated by inhibition of epidermal growth factor receptor in a different cellular context, suggesting a stereotyped response that likely is independent of receptor type or tissue origin. Biologically, Met inhibition led to cell-cycle arrest. Inhibition of Ras-dependent signals and PI3K-dependent signals also resulted in cell-cycle arrest, whereas cells in which Met was inhibited proliferated when Ras or PI3K signaling was active. These findings uncover "dominant" and "recessive" nodes among the numerous oncogenic networks regulated by receptor tyrosine kinases and active in cancer, with the Ras and PI3K pathways as determinants of therapeutic response.

摘要

肿瘤的发生和发展需要积累许多遗传和表观遗传损伤。然而,在某些情况下,癌细胞只依赖于这些病变中的一种来维持其恶性特性,这种依赖性导致致癌基因失活时肿瘤的消退(“致癌基因成瘾”)。确定在转化表型中起作用的许多网络中的哪些节点专门介导对致癌基因中和的这种反应对于识别癌症的脆弱性至关重要。我们使用 Met 受体作为主要模型系统,在依赖致癌受体酪氨酸激酶的各种癌细胞中结合了多重磷酸化蛋白质组学、全基因组表达谱分析和功能测定。我们发现 Met 阻断仅影响 Met 下游信号的有限子集:Met 下游的几个途径几乎没有或没有影响;相反,只有 Ras 或磷酸肌醇 3-激酶 (PI3K) 下游的转导子和转录效应子的受限且途径特异性特征被失活。在不同的细胞环境中抑制表皮生长因子受体也产生了类似的特征,表明这是一种刻板的反应,可能独立于受体类型或组织起源。从生物学上讲,Met 抑制导致细胞周期停滞。抑制 Ras 依赖性信号和 PI3K 依赖性信号也导致细胞周期停滞,而当 Ras 或 PI3K 信号活跃时,抑制 Met 的细胞增殖。这些发现揭示了受受体酪氨酸激酶调节并在癌症中活跃的众多致癌网络中的“显性”和“隐性”节点,Ras 和 PI3K 途径是治疗反应的决定因素。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验