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癌症侵袭与组织重塑——蛋白酶系统与细胞类型的协同作用

Cancer invasion and tissue remodeling--cooperation of protease systems and cell types.

作者信息

Danø K, Rømer J, Nielsen B S, Bjørn S, Pyke C, Rygaard J, Lund L R

机构信息

The Finsen Laboratory, Rigshospitalet, Copenhagen, Denmark.

出版信息

APMIS. 1999 Jan;107(1):120-7. doi: 10.1111/j.1699-0463.1999.tb01534.x.

Abstract

Proteolytic degradation of the extracellular matrix plays a crucial role in both cancer invasion and non-neoplastic tissue remodeling processes. In human cancers the components of matrix degrading protease systems (uPA, uPAR, PAI-1 and MMPs) can be expressed by either the non-neoplastic stromal cells, the cancer cells or both. Studies of the prognostic impact of these components in human cancer and the effect of targeted gene inactivation on cancer metastasis in mice support the assumption that proteases promote cancer progression, independent of whether they are expressed by cancer cells or stromal cells. The pattern of expression of components of protease systems is usually very similar in different cases of the same type of cancer, while it varies between different types of cancer. There are intriguing similarities between the cellular expression pattern of components of protease systems seen in cancer invasion and in certain types of non-neoplastic tissue remodeling. We propose that cancer invasion can be viewed as tissue remodeling gone out of control. The stromal cell involvement in cancer invasion represents a new paradigm with important implications for cancer pathophysiology and cancer therapy.

摘要

细胞外基质的蛋白水解降解在癌症侵袭和非肿瘤性组织重塑过程中都起着关键作用。在人类癌症中,基质降解蛋白酶系统(尿激酶型纤溶酶原激活剂、尿激酶型纤溶酶原激活剂受体、纤溶酶原激活剂抑制物-1和基质金属蛋白酶)的成分可由非肿瘤性基质细胞、癌细胞或两者共同表达。对这些成分在人类癌症中的预后影响以及靶向基因失活对小鼠癌症转移的影响的研究支持了这样一种假设,即蛋白酶促进癌症进展,无论它们是由癌细胞还是基质细胞表达。蛋白酶系统成分的表达模式在同一类型癌症的不同病例中通常非常相似,而在不同类型癌症之间则有所不同。在癌症侵袭和某些类型的非肿瘤性组织重塑中所见的蛋白酶系统成分的细胞表达模式之间存在有趣的相似之处。我们提出,癌症侵袭可被视为失控的组织重塑。基质细胞参与癌症侵袭代表了一种新的范式,对癌症病理生理学和癌症治疗具有重要意义。

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