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首页> 外文期刊>Cancer biology & therapy >Regulation of vascular endothelial growth factor (VEGF) production and angiogenesis by tissue Factor (TF) in SGC-7901 gastric cancer cells.
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Regulation of vascular endothelial growth factor (VEGF) production and angiogenesis by tissue Factor (TF) in SGC-7901 gastric cancer cells.

机译:SGC-7901胃癌细胞中组织因子(TF)对血管内皮生长因子(VEGF)产生和血管生成的调节。

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摘要

Tissue factor (TF), an initiator of the extrinsic coagulation cascade, is expressed in a wide range of cancer cells and plays important roles in cancer progression and metastasis. We demonstrated between TF and vascular endothelial growth factor (VEGF) production differences in four human gastric cell lines. One of these cell lines, SGC-7901, a high TF and VEGF producer, was grown subcutaneously in severe combined immuno-deficient (SCID) mice. The SCID mice generated solid tumors characterized by intense vascularity. In contrast, SGC-7901 cells transfected with antisense TF cDNA generated relatively avascular tumors in SCID mice, as determined by immunohistochemical staining of tumor vascular endothelial cells with anti-VIII factor antibody. To investigate the structure-function relationship between TF and VEGF, the SGC-7901 cell line was transfected with antisense a full-length TF cDNA, a cytoplasmic deletion mutant lacking the distal three serine residues (potential substrates for protein kinase C), or an extracellular domain mutant, which has markedly diminished function for activation of factor X. Cells transfected with the full-length antisense TF sequence produced decreased levels of both TF and VEGF. Transfectants with the extracellular domain mutant produced high levels of VEGF mRNA. However, cells transfected with the cytoplasmic deletion mutant construct produced increased levels of TF, but little or no VEGF. Thus, the cytoplasmic tail of TF may signal VEGF expression in some tumor cells.
机译:组织因子(TF)是外在凝血级联反应的引发剂,在多种癌细胞中表达,并在癌症的进展和转移中起重要作用。我们证明了四种人胃细胞系中的TF和血管内皮生长因子(VEGF)的生产差异。这些细胞系之一SGC-7901是高TF和VEGF产生剂,在严重的联合免疫缺陷(SCID)小鼠中皮下生长。 SCID小鼠产生了以强烈血管为特征的实体瘤。相反,反义TF cDNA转染的SGC-7901细胞在SCID小鼠中产生了相对无血管的肿瘤,这是通过用抗VIII因子抗体对肿瘤血管内皮细胞进行免疫组织化学染色确定的。为了研究TF与VEGF之间的结构-功能关系,将STF-7901细胞系反义全长TF cDNA,缺少远端三个丝氨酸残基(蛋白激酶C的潜在底物)的细胞质缺失突变体,或胞外结构域突变体,其激活X因子的功能明显减弱。用全长反义TF序列转染的细胞产生的TF和VEGF含量均降低。具有细胞外结构域突变体的转染子产生高水平的VEGF mRNA。然而,用细胞质缺失突变体构建体转染的细胞产生增加的TF水平,但是很少或没有VEGF。因此,TF的细胞质尾巴可能在某些肿瘤细胞中表达VEGF的信号。

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