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Topoisomerase IIalpha gene amplification in gastric carcinomas: correlation with the HER2 gene. An immunohistochemical, immunoblotting, and multicolor fluorescence in situ hybridization study.

机译:胃癌拓扑异构酶IIalpha基因扩增:与HER2基因的相关性。免疫组织化学,免疫印迹和多色荧光原位杂交研究。

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摘要

Topoisomerase IIalpha (topoIIalpha) is an enzyme required for DNA replication and a molecular target for drugs called anthracyclines. The topoIIalpha gene (TOP2A) is located close to the HER-2eu oncogene (HER2). We assessed gastric cancers to (1) clarify the relationship between gene amplification and protein overexpression of topoIIalpha and HER2; (2) evaluate the correlation between gene amplification and protein overexpression of topoIIalpha; and (3) examine the relationship between the results of immunohistochemistry and Western blot analysis for topoIIalpha. In a combined analysis of immunohistochemistry and fluorescence in situ hybridization on 552 formalin-fixed and paraffin-embedded gastric cancer tissues, 38 cases were found to have HER2 amplification. Further examination by fluorescence in situ hybridization revealed amplification of TOP2A in 13 of the 38 cases. No aberrations in the TOP2A gene were observed in cases without HER2 overexpression, except for one containing a gene deletion. The TopoIIalpha protein-labeling index was not correlated with TOP2A amplification. Fluorescence in situ hybridization was performed on nuclear imprint specimens obtained from 9 cases using simultaneous probes for TOP2A, HER2, and centromere 17. Of these 9 cases, 3 displayed coamplification of TOP2A and HER2, and only 1 of the 3 cases revealed a high expression of topoIIalpha in Western blot. Although patients having gastric adenocarcinoma with TOP2A amplification could be considered suitable for clinical trials, information involving anthracycline therapy is not firmly understood in regards to the status of TOP2A amplification or protein overexpression. Therefore, results of the current study will provide further insight for the clinical application of anthracycline in gastric cancers.
机译:拓扑异构酶IIalpha(topoIIalpha)是DNA复制所需的酶,是蒽环类药物的分子靶标。 topoIIalpha基因(TOP2A)靠近HER-2 / neu癌基因(HER2)。我们评估了胃癌,以(1)阐明topoIIalpha和HER2的基因扩增与蛋白质过度表达之间的关系; (2)评估topoIIalpha基因扩增与蛋白质过度表达之间的相关性; (3)研究了topoIIalpha的免疫组化结果和Western blot分析之间的关系。在对552份福尔马林固定和石蜡包埋的胃癌组织进行免疫组织化学和荧光原位杂交的组合分析中,发现38例HER2扩增。通过荧光原位杂交进一步检查发现38例中有13例TOP2A扩增。在没有HER2过表达的情况下,除了一个含有基因缺失的病例外,未观察到TOP2A基因异常。 TopoIIalpha蛋白标记指数与TOP2A扩增无关。使用TOP2A,HER2和着丝粒17的同时探针对9例获得的核印迹标本进行荧光原位杂交。这9例中,有3例显示TOP2A和HER2的共扩增,只有3例显示高表达免疫印迹中topoIIalpha的表达。尽管具有TOP2A扩增的胃腺癌患者可能被认为适合进行临床试验,但是关于TOP2A扩增或蛋白过表达的状态,尚不完全了解涉及蒽环类药物治疗的信息。因此,本研究的结果将为蒽环类药物在胃癌中的临床应用提供进一步的认识。

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