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Glucose transporter protein 1 expression in mucoepidermoid carcinoma of salivary gland: correlation with grade of malignancy

机译:涎腺粘液表皮样癌中葡萄糖转运蛋白1的表达与恶性程度的关系

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摘要

Mucoepidermoid carcinoma (MEC), the most common primary salivary malignancy, shows great variability in clinical behaviour, thus demanding investigation to identify of prognostic markers. Since Warburg's studies, unrestricted cell growth during tumorigenesis has been linked to altered metabolism, implying hypoxic stimulation of glycolysis and diminished contribution of mitochondrial oxidative phosphorylation to cellular ATP supply. Hypothesizing that the study of MEC metabolic status could lead to the discovery of prognostic markers, we investigated by immunohistochemistry the expression of glucose transporter 1 (Glut-1), mitochondrial antigen and peroxiredoxin I (Prx I) in samples of MEC from different histological grades. Our results showed that mitochondrial antigen and Prx I were expressed in the majority of the MEC cases independent of the histological grade. In contrast Glut-1 expression increased significantly as the tumours became more aggressive. These results suggested that oxidative phosphorylation may contribute to ATP supply in all stages of MEC progression, and that the relative contribution of glycolysis over mitochondria for cellular ATP supply increases during MEC progression, favouring growth under low oxygen concentration. In addition, the observed high Prx I protein levels could provide protection to tumour cells against reactive oxygen species generated as a consequence of mitochondrial function and hypoxia-reoxygenation cycling. Altogether our findings suggest that upregulation of Glut-1 and Prx I constitute successful adaptive strategies of MEC cells conferring a growth advantage over normal salivary gland cells in the unstable oxygenation tumour environment.
机译:黏液表皮样癌(MEC)是最常见的原发性涎腺恶性肿瘤,在临床表现上表现出很大的变异性,因此需要进行研究以鉴定预后指标。自Warburg进行研究以来,肿瘤发生过程中不受限制的细胞生长与代谢改变有关,这暗示了糖酵解的低氧刺激和线粒体氧化磷酸化对细胞ATP供应的贡献减少。推测MEC代谢状态的研究可能导致发现预后标志物,我们通过免疫组化研究了不同组织学级别的MEC样品中葡萄糖转运蛋白1(Glut-1),线粒体抗原和过氧化物酶I(Prx I)的表达。 。我们的结果表明,线粒体抗原和Prx I在大多数MEC病例中表达,与组织学等级无关。相反,随着肿瘤变得更具侵略性,Glut-1表达显着增加。这些结果表明,氧化磷酸化可能在MEC进展的所有阶段均有助于ATP的供应,而糖酵解对线粒体的细胞ATP供应的相对贡献在MEC进展期间增加,有利于低氧浓度下的生长。此外,观察到的高Prx I蛋白水平可以为肿瘤细胞提供保护,使其免受线粒体功能和缺氧-复氧循环所产生的活性氧的影响。总的来说,我们的发现表明,在不稳定的氧合肿瘤环境中,Glut-1和Prx I的上调构成了MEC细胞成功的适应策略,赋予了其比正常唾液腺细胞更大的生长优势。

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