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c-Src and cooperating partners in human cancer.

机译:c-Src及其在人类癌症中的合作伙伴。

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摘要

The proto-oncogene c-src is rarely mutated in human cancers, and when overexpressed in normal cells is non- or weakly oncogenic. These observations have raised doubts about the involvement of c-src in the etiology of human tumors. However, recent studies have shown that c-Src, a non-receptor tyrosine kinase, exhibits elevated protein levels and activity in numerous types of human cancers. Furthermore, it has been found to be a critical component of multiple signaling pathways that regulate proliferation, survival, metastasis, and angiogenesis. Because of its important role in these oncogenic processes, it represents a therapeutic target ripe for exploitation.
机译:原癌基因c-src在人类癌症中很少发生突变,当在正常细胞中过表达时,它是非致癌或弱致癌基因。这些观察结果引起了对c-src参与人类肿瘤病因学的怀疑。但是,最近的研究表明,c-Src(一种非受体酪氨酸激酶)在许多类型的人类癌症中均表现出较高的蛋白质水平和活性。此外,已发现它是调节增殖,存活,转移和血管生成的多种信号通路的关键组成部分。由于其在这些致癌过程中的重要作用,它代表了成熟的治疗靶标。

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