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肝细胞生长因子-散射因子在肿瘤侵袭和血管生成中与其他细胞因子的相互作用。

The interaction of HGF-SF with other cytokines in tumor invasion and angiogenesis.

作者信息

Rosen E M, Zitnik R J, Elias J A, Bhargava M M, Wines J, Goldberg I D

机构信息

Department of Therapeutic Radiology, Yale University School of Medicine, New Haven, CT 06510.

出版信息

EXS. 1993;65:301-10.

PMID:7678533
Abstract

Scatter factor (SF) is a glycoprotein which is secreted by mesenchymal cells and which causes cohesive epithelial cell colonies to spread out, separate into individual cells, and assume a fibroblastic morphology (i.e., to "scatter"). SF is now known to be identical or nearly identical to hepatocyte growth factor, a serum-derived mitogen for various normal cell types. SF, tumor necrosis factor-alpha (TNFa), and interleukin-1 (IL1) share the ability to stimulate scattering, motility, and protease production in a variety of human tumor cell types. SF and TNFa stimulate vascular endothelial cell motility in vitro and induce angiogenesis, the formation of new blood vessels, in vivo. These factors may participate in a cytokine network which regulates tumor invasion and metastasis directly by enhancing the malignant epithelial phenotype and indirectly by inducing tumor neovascularization.

摘要

散射因子(SF)是一种糖蛋白,由间充质细胞分泌,可使紧密相连的上皮细胞集落散开,分离成单个细胞,并呈现成纤维细胞形态(即“散射”)。现在已知SF与肝细胞生长因子相同或几乎相同,肝细胞生长因子是一种血清来源的促有丝分裂原,对多种正常细胞类型起作用。SF、肿瘤坏死因子-α(TNFα)和白细胞介素-1(IL1)都具有刺激多种人类肿瘤细胞类型发生散射、迁移和产生蛋白酶的能力。SF和TNFα在体外刺激血管内皮细胞迁移,并在体内诱导血管生成,即新血管的形成。这些因子可能参与了一个细胞因子网络,该网络通过增强恶性上皮表型直接调节肿瘤侵袭和转移,并通过诱导肿瘤新生血管形成间接调节肿瘤侵袭和转移。

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