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Differential effect of hypoxia and acidity on lung cancer cell and fibroblast metabolism

机译:缺氧与酸度对肺癌细胞和成纤维细胞代谢的差异效应

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This study examined the metabolic response of lung cancer cells and normal lung fibroblasts to hypoxia and acidity. GLUT1 and HXKII mRNA/protein expression was up-regulated under hypoxia in the MRC5 fibroblasts and in the A549 and H1299 lung cancer cell lines, indicating intensified glucose absorption and glycolysis. Under hypoxia, the LDHA mRNA and LDH5 protein levels increased in the cancer cells but not in the fibroblasts. Acidity suppressed the above-mentioned hypoxia effect. PDH-kinase-1 (PDK1 mRNA and protein) and inactive phosphorylated-PDH protein levels were induced under hypoxia in the cancer cells, whereas these were reduced in the MRC5 lung fibroblasts. In human tissue sections, the prevalent expression patterns supported the contrasting metabolic behavior of cancer cells vs. tumor fibroblasts. The monocarboxylate/lactate transporter 1 (MCT1) was up-regulated in all the cell lines under hypoxic conditions, but it was suppressed under acidic conditions. The mitochondrial DNA (mtDNA) content per cell decreased significantly in the A549 cancer cell line under hypoxia, but it increased in the MRC5 fibroblasts. Taking into account these findings, we suggest that, under hypoxia, cancer cells intensify the anaerobic direction in glycolysis, while normal fibroblasts prefer to seek energy by intensifying the aerobic use of the available oxygen.
机译:该研究检测了肺癌细胞和正常肺成纤维细胞对缺氧和酸度的代谢反应。在MRC5成纤维细胞和A549和H1299肺癌细胞系中,在缺氧下抑制无菌1和HXKII mRNA /蛋白表达,表明加强葡萄糖吸收和糖酵解。在缺氧下,癌细胞中的LDHA mRNA和LDH5蛋白水平增加但不在成纤维细胞中增加。酸度抑制了上述缺氧效应。在癌细胞的缺氧下诱导PDH-激酶-1(PDK1 mRNA和蛋白)和无活性磷酸化-PDH蛋白水平,而这些在MRC5肺成纤维细胞中降低。在人体组织切片中,普遍的表达模式支持癌细胞与肿瘤成纤维细胞的对比代谢行为。在缺氧条件下,单羧酸/乳酸转运蛋白1(MCT1)上调,但在酸性条件下抑制它。在缺氧下A549癌细胞系中,每种细胞的线粒体DNA(MTDNA)含量显着下降,但在MRC5成纤维细胞中增加。考虑到这些发现,我们建议,在缺氧下,癌细胞在糖醇分解中加剧了厌氧方向,而正常成纤维细胞更倾向于通过强化可用氧气的有氧用途寻求能量。

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