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IV型胶原α3(IV)链非胶原结构域的特定序列可抑制肿瘤细胞中基质金属蛋白酶的表达和激活。

A specific sequence of the noncollagenous domain of the alpha3(IV) chain of type IV collagen inhibits expression and activation of matrix metalloproteinases by tumor cells.

作者信息

Pasco S, Han J, Gillery P, Bellon G, Maquart F X, Borel J P, Kefalides N A, Monboisse J C

机构信息

Lab Biochemistry, IFR 53 Biomolecules, CNRS UPRESA 6021, UFR Medicine, Reims, France.

出版信息

Cancer Res. 2000 Jan 15;60(2):467-73.

Abstract

The invasive properties of melanoma cells correlate with the expression of matrix metalloproteinases (MMPs) and their physiological modulators (tissue inhibitors of metalloproteinase and membrane-type MMPs) and with that of the alphaVbeta3 integrin. We investigated the effect of anterior lens capsule type IV collagen and of the alpha3(IV) collagen chain on the invasive properties of various tumor cell lines (HT-144 melanoma cells, HT-1080 fibrosarcoma cells). We demonstrated that anterior lens capsule type IV collagen or specifically the synthetic peptide alpha3(IV) 185-203 inhibited both the migration of melanoma or fibrosarcoma cells as well as the activation of membrane-bound MMP-2 by decreasing the expressions of MT1-MMP and the beta3 integrin subunit.

摘要

黑色素瘤细胞的侵袭特性与基质金属蛋白酶(MMPs)及其生理调节剂(金属蛋白酶组织抑制剂和膜型MMPs)的表达以及αVβ3整合素的表达相关。我们研究了前囊膜IV型胶原和α3(IV)胶原链对各种肿瘤细胞系(HT-144黑色素瘤细胞、HT-1080纤维肉瘤细胞)侵袭特性的影响。我们证明,前囊膜IV型胶原或特定的合成肽α3(IV)185 - 203通过降低MT1-MMP和β3整合素亚基的表达,抑制了黑色素瘤或纤维肉瘤细胞的迁移以及膜结合MMP-2的激活。

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