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转化生长因子-β对人结肠癌细胞癌胚抗原分泌的诱导及蛋白质分泌/表达和纤连蛋白/层粘连蛋白表达的调节

Induction of carcinoembryonic antigen secretion and modulation of protein secretion/expression and fibronectin/laminin expression in human colon carcinoma cells by transforming growth factor-beta.

作者信息

Chakrabarty S, Tobon A, Varani J, Brattain M G

机构信息

Bristol-Baylor Laboratory, Department of Pharmacology, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Cancer Res. 1988 Jul 15;48(14):4059-64.

PMID:3289738
Abstract

We have recently reported that TGF-beta induces a response similar to that of planar polar differentiation promoters in human colon carcinoma MOSER cells. N,N-Dimethylformamide and TGF-beta had similar effects on MOSER cells with respect to reversible inhibition of growth (both in monolayer culture and semisolid medium), induction of fibronectin expression and the induction of morphological alterations (Cancer Res., 47:2950-2954, 1987). Since the expression of carcinoembryonic antigen (CEA) has been reported to be modulated by planar polar compounds that promote differentiation in colon carcinomas, we addressed the issue of whether the differentiation-like effects of TGF-beta on these cells would also encompass modulation of CEA expression in the MOSER cells. The biological modulating effects of TGF-beta on extracellular matrix glycoprotein expression and the expression and secretion of cellular proteins were also studied in view of the reported modulating effects of this growth factor on untransformed, noncolonic cells. In this communication we report that TGF-beta induced the synthesis of fibronectin and laminin but not collagen IV. TGF-beta also induced CEA secretion in a dose-dependent manner. Elevated CEA secretion was detected following 48 h of TGF-beta treatment and a 16-fold increase in CEA secretion was observed following 7 days of treatment. The cells were committed to secrete CEA following one dose of TGF-beta treatment. The enhanced expression of four cellular proteins (Mr 42,000, Mr 48,000, Mr 52,000, and Mr 55,000) and the enhanced secretion of three proteins (Mr 66,000, Mr 200,000, and Mr 400,000) were also induced. Some of these protein alterations were detected as early as 6-24 h following TGF-beta treatment. It is concluded that TGF-beta modulated the production and secretion of CEA, the synthesis of fibronectin and laminin, and the expression and secretion of several cellular proteins in the colon carcinoma MOSER cells. To our knowledge, this is the first report on the modulation of CEA and laminin by TGF-beta in tissue-cultured cells, and is the first report on the modulation of cellular proteins by this growth factor in human colon carcinoma cells.

摘要

我们最近报道,在人结肠癌MOSER细胞中,转化生长因子-β(TGF-β)可诱导出与平面极性分化启动子类似的反应。N,N-二甲基甲酰胺和TGF-β对MOSER细胞在生长可逆抑制方面(单层培养和半固体培养基中均如此)、纤连蛋白表达的诱导以及形态学改变的诱导方面具有相似作用(《癌症研究》,47:2950 - 2954,1987)。由于据报道癌胚抗原(CEA)的表达受促进结肠癌分化的平面极性化合物调节,我们探讨了TGF-β对这些细胞的类分化作用是否也包括对MOSER细胞中CEA表达的调节。鉴于该生长因子对未转化的非结肠细胞的调节作用已见报道,我们还研究了TGF-β对细胞外基质糖蛋白表达以及细胞蛋白质表达和分泌的生物学调节作用。在本通讯中,我们报道TGF-β诱导了纤连蛋白和层粘连蛋白的合成,但未诱导IV型胶原的合成。TGF-β还以剂量依赖方式诱导CEA分泌。TGF-β处理48小时后检测到CEA分泌升高,处理7天后观察到CEA分泌增加了16倍。经一剂TGF-β处理后,细胞即开始分泌CEA。还诱导了四种细胞蛋白(分子量42,000、48,000、52,000和55,000)表达增强以及三种蛋白(分子量66,000、200,000和400,000)分泌增强。其中一些蛋白变化在TGF-β处理后6 - 24小时即可检测到。结论是,TGF-β调节了结肠癌MOSER细胞中CEA的产生和分泌、纤连蛋白和层粘连蛋白的合成以及几种细胞蛋白的表达和分泌。据我们所知,这是关于TGF-β在组织培养细胞中调节CEA和层粘连蛋白的首次报道,也是关于该生长因子在人结肠癌细胞中调节细胞蛋白的首次报道。

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