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首页> 外文期刊>American Journal of Pathology: Official Publication of the American Association of Pathologists >Overexpression of pyruvate dehydrogenase kinase 3 increases drug resistance and early recurrence in colon cancer.
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Overexpression of pyruvate dehydrogenase kinase 3 increases drug resistance and early recurrence in colon cancer.

机译:丙酮酸脱氢酶激酶3的过度表达增加了结肠癌的耐药性和早期复发。

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摘要

The switch of cellular metabolism from mitochondrial respiration to glycolysis is the hallmark of cancer cells and is associated with tumor malignancy. Pyruvate dehydrogenase kinase-1 (PDK1) and PDK3 participate in the metabolic switch of cancer cells; however, the medical significance of PDK1 and PDK3 in cancer progression is not known. Here, we assessed the expression profiles of PDK1 and PDK3 in colorectal cancer. Western blot analysis (n = 74) demonstrated that PDK3 was markedly increased in colon cancer compared to that in adjacent normal tissues, whereas PDK1 was decreased in cancer cells. In addition, PDK3 expression was positively correlated with that of hypoxia inducible factor-1alpha (HIF-1alpha) in cancer cells. Further analysis using immunohistochemical staining revealed that PDK3 levels were positively associated with severity of cancer and negatively associated with disease-free survival. In vitro studies using several colon cancer cell lines showed that PDK3 expression was controlled by HIF-1alpha and contributed to hypoxia-induced increased drug resistance, perhaps explaining why patients with PDK3 overexpression have a greater incidence of treatment failure. Taken together, our findings suggest that PDK3 plays an important role in the metabolic switch and drug resistance of colon cancer and is potentially a novel target for cancer therapy.
机译:从线粒体呼吸到糖酵解的细胞代谢切换是癌细胞的标志,与肿瘤恶性肿瘤有关。丙酮酸脱氢酶激酶-1(PDK1)和PDK3参与癌细胞的代谢交换机;然而,癌症进展中PDK1和PDK3的医学意义尚不清楚。在这里,我们评估了结直肠癌中PDK1和PDK3的表达谱。与在相邻的正常组织中相比,蛋白质印迹分析(n = 74)证明了结肠癌的PDK3在结肠癌中显着增加,而PDK1在癌细胞中降低。此外,PDK3表达与癌细胞中的缺氧诱导因子-1Alpha(HIF-1α)正相关。通过免疫组织化学染色的进一步分析显示,PDK3水平与癌症的严重程度正相关,与无病生存率负相关。使用几种结肠癌细胞系的体外研究表明,PDK3表达由HIF-1αcread控制并导致缺氧诱导的耐药性增加,也许解释为什么PDK3过表达的患者具有更大的治疗失败发生率。我们的研究结果表明,PDK3在结肠癌的代谢开关和耐药性中起重要作用,并且是癌症治疗的新靶点。

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