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α2β1整合素的重新表达消除了乳腺癌细胞的恶性表型。

Re-expression of the alpha 2 beta 1 integrin abrogates the malignant phenotype of breast carcinoma cells.

作者信息

Zutter M M, Santoro S A, Staatz W D, Tsung Y L

机构信息

Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 Aug 1;92(16):7411-5. doi: 10.1073/pnas.92.16.7411.

Abstract

To assess the role of altered alpha 2 beta 1 integrin expression in breast cancer, we expressed the alpha 2 beta 1 integrin de novo in a poorly differentiated mammary carcinoma that expressed no detectable alpha 2-integrin subunit. Expression of the alpha 2 beta 1 integrin resulted in a dramatic phenotypic alteration from a fibroblastoid, spindle-shaped, non-contact-inhibited, motile, and invasive cell to an epithelioid, polygonal-shaped, contact-inhibited, less motile, and less invasive cell. Although expression of the alpha 2 subunit did not alter adhesion to collagen, it profoundly altered cell spreading. Re-expression of the alpha 2 beta 1 integrin restored the ability to differentiate into gland-like structures in three-dimensional matrices and markedly reduced the in vivo tumorigenicity of the cells. These results indicate that the consequences of diminished alpha 2 beta 1-integrin expression in the development of breast cancer and, presumably, of other epithelial malignancies are increased tumorigenicity and loss of the differentiated epithelial phenotype.

摘要

为评估α2β1整合素表达改变在乳腺癌中的作用,我们在一个未检测到α2整合素亚基表达的低分化乳腺癌中重新表达了α2β1整合素。α2β1整合素的表达导致了显著的表型改变,从成纤维细胞样、纺锤形、非接触抑制、有运动性和侵袭性的细胞转变为上皮样、多边形、接触抑制、运动性较低和侵袭性较低的细胞。虽然α2亚基的表达并未改变对胶原蛋白的黏附,但它深刻地改变了细胞铺展。α2β1整合素的重新表达恢复了在三维基质中分化为腺样结构的能力,并显著降低了细胞的体内致瘤性。这些结果表明,α2β1整合素表达减少在乳腺癌以及可能在其他上皮性恶性肿瘤发生发展中的后果是致瘤性增加和分化上皮表型丧失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a75/41349/3aa9791f336b/pnas01494-0285-a.jpg

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