Park K, Kim S J, Bang Y J, Park J G, Kim N K, Roberts A B, Sporn M B
Laboratory of Chemoprevention, National Cancer Institute, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):8772-6. doi: 10.1073/pnas.91.19.8772.
We have found several genetic changes in the TGF-beta-type II receptor gene in human gastric cancer cell lines resistant to the growth inhibitory effect of TGF-beta. Southern blot analysis showed deletion of the type II receptor gene in two of eight cell lines and amplification in another two lines. The single cell line we studied that is sensitive to growth inhibition by TGF-beta showed no structural abnormalities of the type II receptor gene. Some of the gastric cancer cells resistant to the growth inhibitory effect of TGF-beta express either truncated or no detectable TGF-beta type II receptor mRNAs, whereas the one that retains responsiveness to the growth inhibitory effect of TGF-beta expresses a full-size type II receptor mRNA. Immunoprecipitation followed by Western blot analysis showed parallel changes in TGF-beta type II receptor expression. Our results suggest that one of the possible mechanisms of escape from autocrine or paracrine growth control by TGF-beta during carcinogenesis could involve genetic changes in the TGF-beta type II receptor gene itself or altered expression of its mRNA.
我们在对转化生长因子-β(TGF-β)的生长抑制作用具有抗性的人胃癌细胞系中发现了转化生长因子-βⅡ型受体基因的几种遗传变化。Southern印迹分析显示,在八个细胞系中的两个中Ⅱ型受体基因发生缺失,另外两个细胞系中该基因发生扩增。我们研究的对TGF-β生长抑制敏感的单个细胞系未显示Ⅱ型受体基因的结构异常。一些对TGF-β生长抑制作用具有抗性的胃癌细胞表达截短的或无法检测到的TGF-βⅡ型受体mRNA,而对TGF-β生长抑制作用保持反应性的细胞系则表达全长Ⅱ型受体mRNA。免疫沉淀后进行的Western印迹分析显示TGF-βⅡ型受体表达有平行变化。我们的结果表明,在致癌过程中逃避TGF-β自分泌或旁分泌生长控制的一种可能机制可能涉及TGF-βⅡ型受体基因本身的遗传变化或其mRNA表达的改变。