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Differential prognostic impact of hypoxia induced and diffuse HIF-1α expression in invasive breast cancer

机译:低氧诱导的弥漫性HIF-1α在浸润性乳腺癌中的预后影响

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摘要

>Background: Intratumorous hypoxia triggers a broad cellular response mediated by the transcription factor hypoxia inducible factor 1 (HIF-1). HIF-1α concentrations increase during breast carcinogenesis, and are associated with poor prognosis. An earlier study noted two HIF-1α overexpression patterns: diffuse scattered throughout the tissue and confined to perinecrotic cells.>Aims: To investigate the prognostic impact of these different HIF-1α overexpression patterns in relation to its downstream effectors carbonic anhydrase (CA) IX and glucose transporter 1 (GLUT-1).>Methods: HIF-1α, CA IX, and GLUT-1 expression was studied by immunohistochemistry, including double staining for CA IX and HIF-1α. Clinical data included disease free survival, lymph node status, and tumour size.>Results: HIF-1α overexpression (44% of cases) had a perinecrotic (13.5%) or diffuse staining pattern (30.5%). CA IX expression was detectable in 12.5% of breast cancers, whereas GLUT-1 expression was seen in 29%, with both showing perinecrotic membrane staining. Perinecrotic HIF-1α overexpression was highly associated with CA IX and GLUT-1 overexpression, and double staining for HIF-1α and CA IX showed strong expression in the same cells. Diffusely overexpressed HIF-1α was not associated with CA IX or GLUT-1 expression. Patients with diffuse HIF-1α staining had a significantly better prognosis than patients with perinecrotically overexpressed HIF-1α.>Conclusions: Different regulation pathways of HIF-1α overexpression exist in breast cancer: (1) hypoxia induced, perinecrotic HIF-1α overexpression with strong expression of hypoxia associated genes (CA IX and GLUT-1), which is associated with a poor prognosis; and (2) diffuse HIF-1α overexpression lacking major hypoxia associated downstream effects, resulting in a more favourable prognosis.
机译:>背景:瘤内低氧触发由转录因子低氧诱导因子1(HIF-1)介导的广泛细胞反应。 HIF-1α浓度在乳腺癌发生过程中增加,并与不良预后相关。较早的一项研究指出了两种HIF-1α过表达模式:散布在整个组织中并局限于坏死性坏死细胞。>目的:研究这些不同的HIF-1α过表达模式对其下游效应子的预后影响。碳酸酐酶(CA)IX和葡萄糖转运蛋白1(GLUT-1)。>方法:通过免疫组化研究了HIF-1α,CA IX和GLUT-1的表达,包括对CA IX和HIF的双重染色-1α。临床数据包括无病生存期,淋巴结状态和肿瘤大小。>结果:HIF-1α过表达(占病例的44%)有坏死性坏死(13.5%)或弥漫性染色(30.5%)。在12.5%的乳腺癌中可检测到CA IX表达,而在29%的患者中可检测到GLUT-1表达,两者均显示出坏死膜染色。坏死性HIF-1α过表达与CA IX和GLUT-1过表达高度相关,HIF-1α和CA IX的双重染色在同一细胞中强表达。弥漫性过表达的HIF-1α与CA IX或GLUT-1表达无关。 HIF-1α弥漫性染色的患者预后明显高于癌旁高表达的HIF-1α。>结论:乳腺癌中存在HIF-1α高表达的不同调节途径:(1)缺氧诱导的股骨头坏死HIF-1α过度表达与缺氧相关基因(CA IX和GLUT-1)的表达强相关,预后不良; (2)弥漫性HIF-1α过表达缺乏严重的缺氧相关的下游作用,从而预后更好。

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