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基质金属蛋白酶-2表达的组织抑制剂对人黑色素瘤细胞系生长和自发转移的影响。

Effect of tissue inhibitor of the matrix metalloproteinases-2 expression on the growth and spontaneous metastasis of a human melanoma cell line.

作者信息

Montgomery A M, Mueller B M, Reisfeld R A, Taylor S M, DeClerck Y A

机构信息

Scripps Research Institute, Department of Immunology, La Jolla, California 92037.

出版信息

Cancer Res. 1994 Oct 15;54(20):5467-73.

PMID:7923181
Abstract

In this study, we examined the effect of expression of tissue inhibitor of metalloproteinases-2 (TIMP-2) on the growth and dissemination of a highly metastatic human melanoma cell line (M24net). M24net melanoma cells express a number of matrix metalloproteinases (MMPs), including gelatinase A and B (MMP-2 and MMP-9) and interstitial collagenase (MMP-1) (A. M. P. Montgomery et al., Cancer Res., 53: 693-700, 1993). The activity of these proteases was effectively down-regulated by transfecting M24net cells with complementary DNA-encoding human TIMP-2. Overexpression of TIMP-2 markedly reduced melanoma growth in the skin of immunodeficient mice but did not prevent these highly malignant cells from spontaneously metastasizing to the lungs and lymph nodes of inoculated mice. We provide a mechanism to account for the growth inhibitory property of TIMP-2 based on its ability to regulate M24net cell growth in three-dimensional interstitial collagen. In the presence of this matrix, M24net cells assume a differentiated morphology and have a reduced growth rate. We present evidence that overexpression of TIMP-2 increases the susceptibility of M24net cells to growth inhibition and morphological differentiation by occluding interstitial collagen.

摘要

在本研究中,我们检测了金属蛋白酶组织抑制因子-2(TIMP-2)的表达对高转移性人黑色素瘤细胞系(M24net)生长和扩散的影响。M24net黑色素瘤细胞表达多种基质金属蛋白酶(MMPs),包括明胶酶A和B(MMP-2和MMP-9)以及间质胶原酶(MMP-1)(A.M.P.蒙哥马利等人,《癌症研究》,53:693-700,1993)。通过用编码人TIMP-2的互补DNA转染M24net细胞,这些蛋白酶的活性被有效下调。TIMP-2的过表达显著降低了免疫缺陷小鼠皮肤中黑色素瘤的生长,但并未阻止这些高恶性细胞自发转移至接种小鼠的肺和淋巴结。我们基于TIMP-2调节M24net细胞在三维间质胶原中生长的能力,提供了一种解释TIMP-2生长抑制特性的机制。在这种基质存在的情况下,M24net细胞呈现分化形态且生长速率降低。我们提供的证据表明,TIMP-2的过表达通过封闭间质胶原增加了M24net细胞对生长抑制和形态分化的敏感性。

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