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首页> 外文期刊>British Journal of Cancer >The key hypoxia regulated gene CAIX is upregulated in basal-like breast tumours and is associated with resistance to chemotherapy
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The key hypoxia regulated gene CAIX is upregulated in basal-like breast tumours and is associated with resistance to chemotherapy

机译:关键的低氧调节基因CAIX在基底样乳腺肿瘤中上调,并与化疗耐药相关

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摘要

Basal-like tumours account for 15% of invasive breast carcinomas and are associated with a poorer prognosis and resistance to therapy. We hypothesised that this aggressive phenotype is because of an intrinsically elevated hypoxic response. Microarrayed tumours from 188 patients were stained for hypoxia-inducible factor (HIF)-1α, prolyl hydroxylase (PHD)1, PHD2, PHD3 and factor inhibiting HIF (FIH)-1, and carbonic anhydrase (CA) IX stained in 456 breast tumours. Tumour subtypes were correlated with standard clincopathological parameters as well as hypoxic markers. Out of 456 tumours 62 (14%) tumours were basal-like. These tumours were positively correlated with high tumour grade (PPα, and more than half expressed at least one of the PHD enzymes and FIH-1. Basal-like tumours were nine times more likely to be associated with CAIX expression (PP=0.005), tumour grade (PPPP=0.03, respectively). The association between basal phenotype and CAIX suggests that the more aggressive behaviour of these tumours is partly due to an enhanced hypoxic response. Further, the association with chemoresistance in CAIX-positive breast tumours and basal-like tumours in particular raises the possibility that targeted therapy against HIF pathway or downstream genes such as CAs may be an approach to investigate for these patients.
机译:基底样肿瘤占浸润性乳腺癌的15%,并与预后较差和对治疗的抵抗力有关。我们假设这种积极的表型是由于内在缺氧反应的升高。对188位患者的微阵列肿瘤进行了缺氧诱导因子(HIF)-1α,脯氨酰羟化酶(PHD)1,PHD2,PHD3和抑制因子HIF(FIH)-1和碳酸酐酶(CA)IX染色的456例乳腺肿瘤。肿瘤亚型与标准临床病理参数以及低氧标志物相关。在456个肿瘤中,有62个(14%)肿瘤为基底样肿瘤。这些肿瘤与高肿瘤分级(PPα)呈正相关,一半以上表达至少一种PHD酶和FIH-1;基底样肿瘤与CAIX表达相关的可能性高9倍(PP = 0.005),肿瘤分级(分别为PPPP = 0.03)。基础表型与CAIX之间的相关性表明,这些肿瘤更具侵略性的行为部分是由于缺氧反应增强所致;此外,CAIX阳性乳腺肿瘤和基础-乳腺癌中与化学耐药性的相关性特别是像肿瘤这样的肿瘤,增加了针对HIF途径或下游基因(例如CAs)的靶向治疗可能是针对这些患者进行研究的一种方法。

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