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Expression of the pro-angiogenic factors vascular endothelial growth factor and interleukin-8/CXCL8 by human breast carcinomas is responsive to nutrient deprivation and endoplasmic reticulum stress

机译:人乳腺癌中促血管生成因子血管内皮生长因子和白介素8 / CXCL8的表达对营养缺乏和内质网应激有反应

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摘要

BackgroundThe expression of pro-angiogenic cytokines, such as vascular endothelial growth factor (VEGF) and interleukin-8/CXCL8 (IL-8), plays an important role in tumor growth and metastasis. Low oxygen tension within poorly-vascularized tumors is thought to be the prime stimulus causing the secretion of VEGF. The expression of IL-8 by solid tumors is thought to be primarily due to intrinsic influences, such as constitutive activation of nuclear factor kappa B (NF-κB). However, VEGF expression is responsive to glucose deprivation, suggesting that low concentrations of nutrients other than oxygen may play a role in triggering the pro-angiogenic phenotype. Glucose deprivation causes endoplasmic reticulum (ER) stress and alters gene expression through the unfolded protein response (UPR) signaling pathway. A branch of the UPR, known as the ER overload response (EOR), can cause NF-κB activation. Thus, we hypothesized that treatments that cause ER stress and deprivation of other nutrients, such as amino acids, would trigger the expression of angiogenic cytokines by breast cancer cell lines.
机译:背景促血管生成细胞因子的表达,例如血管内皮生长因子(VEGF)和白介素8 / CXCL8(IL-8),在肿瘤的生长和转移中起着重要的作用。血管生成不良的肿瘤中的低氧张力被认为是引起VEGF分泌的主要刺激因素。实体瘤中IL-8的表达被认为主要是由于内在影响,例如核因子κB(NF-κB)的组成性激活。然而,VEGF的表达对葡萄糖的缺乏有反应,表明低浓度的除氧以外的营养物质可能在触发促血管生成表型中起作用。葡萄糖剥夺引起内质网(ER)应激,并通过未折叠的蛋白应答(UPR)信号传导途径改变基因表达。 UPR的一个分支称为ER过载响应(EOR),可引起NF-κB激活。因此,我们假设引起内质网应激和剥夺其他营养物质(例如氨基酸)的治疗将触发乳腺癌细胞系表达血管生成细胞因子。

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