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干扰素可抑制转化细胞的趋化性及其对重组基底膜的侵袭。

Interferons inhibit chemotaxis of transformed cells and their invasion of a reconstituted basement membrane.

作者信息

Melchiori A, Allavena G, Böhm J, Remy W, Schmidt J, Parodi S, Santi L, Albini A

出版信息

Anticancer Res. 1987 May-Jun;7(3 Pt B):475-9.

PMID:2443071
Abstract

Tumor cell migration and invasion are critical steps in the complex process of metastasis formation. It has been demonstrated that interferons (IFNs) inhibit the motility of human fibroblasts. In the present investigation we tested the effect of human leukocyte IFN and murine fibroblast IFN on the chemotactic migration of transformed and tumor-derived cells towards fibroblast conditioned medium. We were able to show that IFNs preferentially inhibit the chemotaxis of transformed and tumor-derived cell lines when compared to control fibroblasts. Inhibition was dose-dependent and most tumor cell strains were sensitive to concentrations of IFNs 10- to 100-fold lower than fibroblast cultures. Furthermore, leukocyte interferon was able to inhibit the invasion of transformed 3T3 fibroblasts through a gel of reconstituted basement membrane (Matrigel). These effects could be related to the antineoplastic activity of interferon.

摘要

肿瘤细胞的迁移和侵袭是转移形成这一复杂过程中的关键步骤。已证实干扰素(IFN)可抑制人成纤维细胞的运动。在本研究中,我们测试了人白细胞干扰素和鼠成纤维细胞干扰素对转化细胞和肿瘤衍生细胞向成纤维细胞条件培养基趋化迁移的影响。我们能够表明,与对照成纤维细胞相比,干扰素优先抑制转化细胞和肿瘤衍生细胞系的趋化作用。抑制作用呈剂量依赖性,大多数肿瘤细胞株对干扰素浓度的敏感性比成纤维细胞培养物低10至100倍。此外,白细胞干扰素能够抑制转化的3T3成纤维细胞穿过重组基底膜(基质胶)凝胶的侵袭。这些效应可能与干扰素的抗肿瘤活性有关。

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