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Requirement of Stat3 but not Stat1 activation for epidermal growth factor receptor- mediated cell growth In vitro.

机译:表皮生长因子受体介导的细胞生长需要Stat3激活而不需要Stat1激活。

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摘要

Stimulation of epidermal growth factor receptor (EGFR) by ligand(s) leads to activation of signaling molecules including Stat1 and Stat3, two members of the signal transducers and activators of transcription (STAT) protein family. Activation of Stat1 and Stat3 was constitutive in transformed squamous epithelial cells, which produce elevated levels of TGF-alpha, and was enhanced by the addition of exogenous TGF-alpha. Targeting of Stat3 using antisense oligonucleotides directed against the translation initiation site, resulted in significant growth inhibition. In addition, cells stably transfected with dominant negative mutant Stat3 constructs failed to proliferate in vitro. In contrast, targeting of Stat1 using either antisense or dominant-negative strategies had no effect on cell growth. Thus, TGF-alpha/EGFR-mediated autocrine growth of transformed epithelial cells is dependent on activation of Stat3 but not Stat1.
机译:配体对表皮生长因子受体(EGFR)的刺激导致包括Stat1和Stat3,信号转导子和转录激活子(STAT)蛋白家族的两个成员在内的信号分子的激活。 Stat1和Stat3的激活在转化的鳞状上皮细胞中是组成性的,其产生水平升高的TGF-α,并通过添加外源性TGF-α增强。使用针对翻译起始位点的反义寡核苷酸靶向Stat3,导致明显的生长抑制。另外,用显性负突变Stat3构建体稳定转染的细胞不能在体外增殖。相反,使用反义或显性负性策略靶向Stat1对细胞生长没有影响。因此,转化生长的上皮细胞的TGF-α/ EGFR介导的自分泌生长依赖于Stat3的激活,而不是Stat1的激活。

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