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癌症中的肌营养不良聚糖复合物

Dystroglycan complex in cancer.

作者信息

Brennan P A, Jing J, Ethunandan M, Górecki D

机构信息

Maxillofacial Unit, Department of Head and Neck Surgery, Queen Alexandra Hospital, Portsmouth PO6 3LY, UK.

出版信息

Eur J Surg Oncol. 2004 Aug;30(6):589-92. doi: 10.1016/j.ejso.2004.03.014.

Abstract

Abnormalities in the interactions between tumour cells, adhesion molecules and extracellular matrix proteins are often implicated in the behaviour of carcinoma cells. The alpha- and beta-dystroglycan (DG) proteins form part of the large dystrophin-associated protein (DAP) complex. They are involved in epithelial cell development, formation of the basement membrane and maintenance of tissue integrity. Specific changes and reduction or loss of DG expression have been reported in human breast, colon, head and neck, and prostate cancers, implicating it in tumour invasion and dissemination. Degradation of beta-DG by matrix metalloproteinase (MMP) enzymes may assist tumour dissemination. We report the present knowledge of the DG interactions in solid tumour biology.

摘要

肿瘤细胞、黏附分子和细胞外基质蛋白之间相互作用的异常常与癌细胞的行为有关。α-和β-肌营养不良聚糖(DG)蛋白是大型肌营养不良蛋白相关蛋白(DAP)复合体的一部分。它们参与上皮细胞发育、基底膜形成和组织完整性的维持。据报道,在人类乳腺癌、结肠癌、头颈癌和前列腺癌中存在DG表达的特异性改变以及表达降低或缺失,这表明其与肿瘤侵袭和扩散有关。基质金属蛋白酶(MMP)对β-DG的降解可能有助于肿瘤扩散。我们报告了目前关于实体瘤生物学中DG相互作用的知识。

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