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An immunohistochemical evaluation of c-erbB-2 expression in human breast carcinoma.

机译:对人乳腺癌中c-erbB-2表达的免疫组织化学评估。

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摘要

The c-erbB-2 gene codes for a putative transmembrane protein, similar in structure to the epidermal growth factor (EGF) receptor. Amplification of the gene has been described in a variety of human adenocarcinomas and is particularly well documented in breast carcinoma. It has been suggested that amplification is indicative of poor prognosis and, as such, is comparable with lymph node status as a predictor of clinical outcome. This study examines the suggestion indirectly by an immunohistochemical technique. Archival tissue from 195 patients with primary breast carcinoma was stained with the polyclonal antibody 21N, raised to amino acids 1243-1255, the C-terminus of the predicted amino acid sequence of the c-erbB-2 protein. Up to 10 year verified follow-up data were available on all patients. Staining compatible with significant amplification was observed in 17 patients. Using the chi-squared test for trend a significant correlation was found between staining and grade (P = 0.04) but not with either node or receptor status. No significant association was found between staining and clinical outcome although there was a tendency for patients with stained tumours to have a worse prognosis. A Cox regression analysis was used to adjust for node status and grade and still no correlation was revealed between staining and prognosis. However a study of this size in which only a small number of patients have been found to have stained tumours does have wide confidence limits. Comparable staining observed in in situ and infiltrating components of tumours suggests that amplification is an early event in carcinogenesis. Similar staining in primary and subsequent metastatic lesions was also noted. It is considered that further studies at both the DNA/mRNA and protein levels are required to confirm the significance of c-erbB-2 amplification in human breast carcinoma.
机译:c-erbB-2基因编码一种假定的跨膜蛋白,其结构与表皮生长因子(EGF)受体相似。该基因的扩增已在多种人类腺癌中进行了描述,在乳腺癌中尤其有据可查。已经提出,扩增指示不良的预后,因此,其可与淋巴结状态相比作为临床结果的预测指标。这项研究通过免疫组织化学技术间接检查了该建议。用多克隆抗体21N对来自195例原发性乳腺癌患者的档案组织进行染色,并将其克隆至氨基酸1243-1255(c-erbB-2蛋白的预测氨基酸序列的C端)。所有患者均可获得长达10年的经过验证的随访数据。在17名患者中观察到与显着扩增相容的染色。使用卡方检验趋势,发现染色和等级之间存在显着相关性(P = 0.04),但与淋巴结或受体状态无关。尽管存在染色肿瘤患者预后较差的趋势,但在染色与临床结果之间未发现显着关联。使用Cox回归分析调整结节状态和等级,但仍未发现染色与预后之间的相关性。但是,只有如此之少的研究发现,只有少数患者的肿瘤被染色,确实有很大的置信度限制。在肿瘤的原位和浸润成分中观察到的可比染色表明,扩增是致癌作用的早期事件。在原发性和随后的转移性病变中也发现了类似的染色。认为需要在DNA / mRNA和蛋白质水平上进行进一步研究,以证实c-erbB-2扩增在人乳腺癌中的重要性。

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