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Diminished expression of integrin adhesion molecules on human colonic epithelial cells during the benign to malign tumour transformation.

机译:在良性到恶性肿瘤转化过程中整合素粘附分子在人结肠上皮细胞上的表达减少。

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摘要

Integrins are transmembrane molecules that mediate cell-cell and cell-substratum adhesion. Because alterations in the adhesive properties of tumour cells are thought to influence tumour cell invasion, the expression of integrin alpha and beta chains in 19 human colorectal carcinomas, eight adenomas, and eight normal colon tissues was examined immunohistochemically using an indirect immunofluorescent technique. Normal colonic epithelial cells were found to express the integrin alpha 3, alpha 5, alpha 6, beta 1, and beta 4 chains, whereas the alpha 2 chain was expressed only on epithelial cells lining the base of the crypts and was absent from cells lining the mouth of the crypts or the surface epithelium. No epithelial staining of the alpha 1, alpha 4, beta 2, and beta 3 chains was observed. A progressive reduction of all normally expressed alpha and beta chains was associated with increasing neoplastic transformation. The expression of the alpha 3 and alpha 5 chains was already noticeably reduced in adenomas, and was completely absent in most colonic carcinomas. In contrast, alpha 6, beta 1, and beta 4 expression was maintained in adenomas, whereas the transformation from benign to malignant neoplasms associated with infiltrative growth was characterised by diminished or lost expression of alpha 6, beta 1, and beta 4 chains. Thus, the decreased expression of integrins in human colon carcinomas may contribute to the altered adhesion and migration properties of these tumour cells.
机译:整联蛋白是介导细胞-细胞和细胞-基质粘附的跨膜分子。由于认为肿瘤细胞粘附特性的改变会影响肿瘤细胞的侵袭,因此采用间接免疫荧光技术对19种人结肠直肠癌,8个腺瘤和8个正常结肠组织中整联蛋白α和β链的表达进行了免疫组织化学检查。发现正常结肠上皮细胞表达整联蛋白α3,α5,α6,β1和β4链,而α2链仅在位于隐窝底部的上皮细胞表达,而在细胞内衬中不存在隐窝口或表面上皮。没有观察到α1,α4,β2和β3链的上皮染色。所有正常表达的α和β链的逐渐减少与肿瘤转化的增加有关。在腺瘤中,α3和α5链的表达已经明显降低,在大多数结肠癌中完全不存在。相反,腺瘤中维持了α6,β1和β4的表达,而与浸润性生长相关的从良性到恶性肿瘤的转化的特征是α6,β1和β4链的表达减少或丢失。因此,人结肠癌中整联蛋白表达的降低可能有助于改变这些肿瘤细胞的粘附和迁移特性。

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