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首页> 外文期刊>Breast cancer research and treatment. >The presence of a fibrotic focus in invasive breast carcinoma correlates with the expression of carbonic anhydrase IX and is a marker of hypoxia and poor prognosis.
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The presence of a fibrotic focus in invasive breast carcinoma correlates with the expression of carbonic anhydrase IX and is a marker of hypoxia and poor prognosis.

机译:浸润性乳腺癌中纤维化病灶的存在与碳酸酐酶IX的表达相关,是缺氧和预后不良的标志。

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摘要

The value of the fibrotic focus (FF) as a marker of intra-tumoral hypoxia in invasive breast carcinoma was assessed by studying its relationship with the expression of the hypoxia-induced carbonic anhydrase IX (CA IX), angiogenesis indices and prognosis. CA IX expression was immunohistochemically detected in 2 independent study groups, totaling 184 patients, and correlated with tumor characteristics, angiogenesis related parameters and patient outcome by univariate analysis. CA IX immunostaining scores in carcinoma cells and in tumoral fibroblasts were significantly higher in expansively growing tumors (p = 0.0001 and p < 10(-4), respectively), containing an FF (p = 0.0004 and p < 10(-4)) and showing high histological grade (p = 0.016 and p = 0.0006). Microvessel density, quantified by Chalkley counting, was correlated with CA IX expression both in the carcinoma cells and in the fibroblasts (p = 0.0076 and p = 0.0025) and with the presence and relative size of an FF (p = 0.006). The fraction of proliferating endothelial cells was positively correlated with CA IX scores in the fibroblasts (r = 0.4, p = 0.02) and with the presence of an FF (p = 0.02). CA IX scores in the fibroblasts--and to a lesser extent in the carcinoma cells--were associated with a higher relapse rate (p = 0.006) and a worse overall survival (p = 0.003). The highest CA IX immunostaining scores were found in the fibroblasts of large FF occupying more than one-third of the tumor. A large FF was associated with worse overall survival in a consecutive patient group (p = 0.01) and with shorter disease-free (p = 0.02) and overall survival (p = 0.0005) in T1-2N0 breast cancer patients. The strong association of CA IX expression with the presence of an FF shows that the latter is a marker of intra-tumoral hypoxia. FF is useful as a surrogate marker of hypoxia-driven ongoing angiogenesis and is associated with a higher relapse rate and a worse overall survival.
机译:通过研究其与低氧诱导的碳酸酐酶IX(CA IX)的表达,血管生成指数和预后的关系,评估纤维化病灶(FF)作为浸润性乳腺癌中肿瘤内低氧的标志物的价值。在2个独立研究组中,共184例患者进行了免疫组化检测CA IX的表达,并通过单因素分析将其与肿瘤特征,血管生成相关参数和患者预后相关。癌细胞和肿瘤成纤维细胞中的CA IX免疫染色评分在肿瘤不断扩大的情况下分别显着较高(分别为p = 0.0001和p <10(-4)),并且含有FF(p = 0.0004和p <10(-4))并显示出较高的组织学等级(p = 0.016和p = 0.0006)。通过Chalkley计数量化的微血管密度与癌细胞和成纤维细胞中的CA IX表达(p = 0.0076和p = 0.0025)以及FF的存在和相对大小(p = 0.006)相关。增殖的内皮细胞分数与成纤维细胞中的CA IX分数呈正相关(r = 0.4,p = 0.02)和FF的存在(p = 0.02)。成纤维细胞中CA IX评分-癌细胞中CA IX评分较低-与较高的复发率(p = 0.006)和较差的总体存活率(p = 0.003)相关。在占肿瘤三分之一以上的大FF的成纤维细胞中发现最高的CA IX免疫染色评分。大的FF与连续患者组的总体生存较差(p = 0.01),T1-2N0乳腺癌患者的无病生存期较短(p = 0.02)和总体生存期较短(p = 0.0005)有关。 CA IX表达与FF的存在密切相关,表明后者是肿瘤内缺氧的标志。 FF可以作为缺氧驱动的正在进行的血管生成的替代指标,并且与更高的复发率和更差的总生存率相关。

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