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胶原酶IV和细胞黏附的抑制剂可降低恶性肿瘤细胞的侵袭活性。

Inhibitors of collagenase IV and cell adhesion reduce the invasive activity of malignant tumour cells.

作者信息

Reich R, Stratford B, Klein K, Martin G R, Mueller R A, Fuller G C

机构信息

Laboratory of Developmental Biology and Anomalies, National Institute of Dental Research, Bethesda, Maryland 20892.

出版信息

Ciba Found Symp. 1988;141:193-210. doi: 10.1002/9780470513736.ch11.

Abstract

The invasive activities of some malignant cells appear to be activated by contact with laminin. This protein occurs solely in basement membranes and the binding of malignant cells to the surface of this extracellular matrix initiates the invasion process. Passage of the cells across basement membrane requires degradative activity and laminin induces the production of collagenase IV which lyses the collagen IV network. The motility of the cells is enhanced by chemo-attractants and by matrix molecules. Peptides that inhibit the binding of tumour cells to laminin, inhibitors of collagenase IV, and inhibitors of specific pathways of arachidonic acid metabolism prevent invasion as well as the metastasis of malignant cells and could be employed to stop the spread of cancer.

摘要

一些恶性细胞的侵袭活性似乎是通过与层粘连蛋白接触而被激活的。这种蛋白质仅存在于基底膜中,恶性细胞与这种细胞外基质表面的结合启动了侵袭过程。细胞穿过基底膜需要降解活性,层粘连蛋白可诱导IV型胶原酶的产生,该酶可分解IV型胶原网络。趋化因子和基质分子可增强细胞的运动性。抑制肿瘤细胞与层粘连蛋白结合的肽、IV型胶原酶抑制剂以及花生四烯酸代谢特定途径的抑制剂可阻止恶性细胞的侵袭和转移,可用于阻止癌症的扩散。

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