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首页> 外文期刊>World Journal of Gastroenterology >Inhibitory effects of EGFR antisense oligodeox- ynucleotide in human colorectal cancer cell line
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Inhibitory effects of EGFR antisense oligodeox- ynucleotide in human colorectal cancer cell line

机译:EGFR反义寡聚核苷酸对人结肠直肠癌细胞系的抑制作用

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摘要

Epidermal-growth-factor receptor~[1] (EGFR) is a polypeptide with 1186 amino acids, which binds to EGF family growth factors. Two major natural Ligands in the family interact with EGFR: one is EGF, the other is transforming growth factor-α (TGF-α)~[2]. When EGF or TGF-α, binds to EGFR, tyrosine kinase activity is induced which in turn triggers a series of events regulating the cell growth~[3-8]. The importance of EGFR in growth regulating pathways was confirmed by the fact that enhanced expression of this receptor was found in brain gliobastomas, breast, lung, ovarian, colorectal, and renal carcinomas.
机译:表皮生长因子受体[1](EGFR)是具有1186个氨基酸的多肽,与EGF家族生长因子结合。该家族中两种主要的天然配体与EGFR相互作用:一种是EGF,另一种是转化生长因子-α(TGF-α)〜[2]。当EGF或TGF-α与EGFR结合时,会诱导酪氨酸激酶活性,进而触发一系列调节细胞生长的事件[3-8]。在脑胶质瘤,乳腺癌,肺癌,卵巢癌,结直肠癌和肾癌中发现了该受体表达增强的事实,证实了EGFR在生长调节通路中的重要性。

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