首页> 外文期刊>Modern Pathology >BRAFV600E mutation influences hypoxia-inducible factor-1|[alpha]| expression levels in papillary thyroid cancer
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BRAFV600E mutation influences hypoxia-inducible factor-1|[alpha]| expression levels in papillary thyroid cancer

机译:BRAFV600E突变影响缺氧诱导因子-1 |α|在甲状腺乳头状癌中的表达水平

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Hypoxia-inducible factor-1α is found frequently overexpressed in solid tumors cells, exerting an important role in angiogenesis, glucose metabolism, cell proliferation, survival and invasion. In thyroid carcinomas, hypoxia-inducible factor-1α expression was found increased in differentiated, poorly differentiated, medullary and anaplastic variants. Hypoxia represents the principal stimulus responsible for hypoxia-inducible factor-1α induction. Other nonhypoxic stimuli increase hypoxia-inducible factor-1α synthesis through the activation of phosphatidylinositol 3-kinase and mitogen-activated protein kinase pathways in a cell-type-specific manner. We have previously shown the role of BRAFV600E mutation in papillary thyroid cancer cells as a factor that facilitates tumor cell growth and progression. In this study, we tested the hypothesis that BRAFV600E mutation influences hypoxia-inducible factor-1α expression in papillary thyroid carcinoma cells. We analyzed 27 papillary thyroid carcinomas, 13 of which presented BRAFV600E mutation. In tumor tissues, immunoreactivity for hypoxia-inducible factor-1α was detected in the majority of analyzed BRAFV600E mutated cases. Transcriptional analyses revealed elevated hypoxia-inducible factor-1α levels with significant differences between wild-type and mutated group. A BRAF wild-type papillary thyroid carcinoma cell line and a BRAFV600E mutated papillary thyroid carcinoma cell line were selected to study the effects of BRAF mutation on hypoxia-inducible factor-1α expression in vitro. Knockdown of mutant BRAFV600E or both the wild type and the BRAFV600E by RNA interference induced a significant reduction of hypoxia-inducible factor-1α expression at mRNA and protein levels. Pharmacological inhibition of BRAF significantly reduces hypoxia-inducible factor-1α expression levels in papillary thyroid carcinoma cell line harboring BRAFV600E mutation. Our results suggest that hypoxia-inducible factor-1α is expressed in papillary thyroid carcinomas and is regulated not only by hypoxia but also by BRAFV600E-mediated signaling pathway.
机译:缺氧诱导因子-1α在实体瘤细胞中经常过度表达,在血管生成,葡萄糖代谢,细胞增殖,存活和侵袭中发挥重要作用。在甲状腺癌中,发现缺氧诱导因子-1α在分化,低分化,髓样和间变性变体中表达增加。缺氧代表负责缺氧诱导因子-1α诱导的主要刺激。其他非缺氧刺激通过以细胞类型特异性方式激活磷脂酰肌醇3激酶和促分裂原活化的蛋白激酶途径来增加缺氧诱导因子1α的合成。我们先前已经显示出BRAFV600E突变在甲状腺乳头状癌细胞中的作用,作为促进肿瘤细胞生长和发展的因素。在这项研究中,我们测试了BRAFV600E突变影响甲状腺乳头状癌细胞中缺氧诱导因子1α表达的假说。我们分析了27例甲状腺乳头状癌,其中13例呈现BRAFV600E突变。在肿瘤组织中,大多数分析过的BRAFV600E突变病例中都检测到了缺氧诱导因子-1α的免疫反应性。转录分析显示缺氧诱导因子-1α水平升高,野生型和突变组之间存在显着差异。选择BRAF野生型甲状腺乳头状癌细胞株和BRAFV600E突变型甲状腺乳头状癌细胞株,以研究BRAF突变对缺氧诱导因子-1α表达的影响。 RNA干扰抑制突变型BRAFV600E或野生型和BRAFV600E均可在mRNA和蛋白水平上显着降低缺氧诱导因子-1α的表达。在含有BRAFV600E突变的甲状腺乳头状癌细胞系中,BRAF的药理抑制作用显着降低了缺氧诱导因子1α的表达水平。我们的结果表明,低氧诱导因子-1α在甲状腺乳头状癌中表达,不仅受低氧调控,而且受BRAFV600E介导的信号通路调控。

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