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首页> 外文期刊>Pathology International >Local balance of transforming growth factor-beta1 secreted from cholangiocarcinoma cells and stromal-derived factor-1 secreted from stromal fibroblasts is a factor involved in invasion of cholangiocarcinoma.
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Local balance of transforming growth factor-beta1 secreted from cholangiocarcinoma cells and stromal-derived factor-1 secreted from stromal fibroblasts is a factor involved in invasion of cholangiocarcinoma.

机译:胆管癌细胞分泌的转化生长因子-beta1和间质成纤维细胞分泌的基质衍生因子-1的局部平衡是胆管癌侵袭的一个因素。

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摘要

Tumor-stromal interactions are important for the progression of malignant tumors. The purpose of the present study was to examine interactions of cholangiocarcinoma (CC) cells and stromal fibroblasts with respect to stromal-derived factor-1 (SDF-1) and transforming growth factor (TGF)-beta1. Two cell lines of CC (HuCCT-1 and CCKS-1) and WI-38 fibroblast cell line were used for cell culture, and 12 CC tissue specimens for immunohistochemical studies. Invasion of CC cells was increased significantly by the supernatant from fibroblast cultures, but not by the supernatant from fibroblasts cocultured with CC cells. Expression of SDF-1 in cultured fibroblasts was downregulated by TGF-beta1 treatment, and coculture with CC cells and anti-TGF-beta1 neutralizing antibody restored the decreased SDF-1 expression, suggesting that TGF-beta1 secreted from CC cells might have reduced the expression of SDF-1 by fibroblasts and might have reduced the increased invasion of CC cells induced by the supernatant from fibroblasts. Immunohistochemical expression of TGF-beta1 in CC cells was focal or negative and that of SDF-1 was evident in stromal fibroblasts at the invasive front of CC. In conclusion, local mutual influence of TGF-beta1 secreted from carcinoma cells and SDF-1 expressed by stromal fibroblasts may be involved in invasion of CC cells.
机译:肿瘤-基质相互作用对恶性肿瘤的进展很重要。本研究的目的是检查胆管癌(CC)细胞和基质成纤维细胞相对于基质衍生因子1(SDF-1)和转化生长因子(TGF)-beta1的相互作用。使用两个CC细胞系(HuCCT-1和CCKS-1)和WI-38成纤维细胞细胞系进行细胞培养,并使用12个CC组织标本进行免疫组织化学研究。来自成纤维细胞培养物的上清液显着增加了CC细胞的侵袭,但未与CC细胞共培养的成纤维细胞的上清液显着增加了CC细胞的侵袭。 TGF-β1处理可下调培养的成纤维细胞中SDF-1的表达,并与CC细胞和抗TGF-β1中和抗体共培养可恢复SDF-1的表达降低,表明CC细胞分泌的TGF-β1可能降低了SDF-1的表达。 SDF-1在成纤维细胞中的表达,并可能减少了由成纤维细胞上清液诱导的CC细胞侵袭的增加。 CC细胞中TGF-β1的免疫组织化学表达呈局灶性或阴性,而在CC侵袭前的基质成纤维细胞中SDF-1明显。总之,癌细胞分泌的TGF-β1和基质成纤维细胞表达的SDF-1的局部相互影响可能参与CC细胞的侵袭。

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