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Variable sensitivity and specificity of TTF-1 antibodies in lung metastatic adenocarcinoma of colorectal origin

机译:TTF-1抗体在大肠源性肺转移性腺癌中的可变敏感性和特异性

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Thyroid transcription factor-1 (TTF-1) is considered as a reliable marker for differential diagnosis in distinguishing primary adenocarcinomas of the lung from extrathoracic origins. We previously reported the first case of lung metastasis of colorectal origin, with nuclear expression of TTF-1. As most previous studies were performed on series of extrathoracic primary tumors, we raised the question of a possible role of lung microenviroment in TTF-1 expression. We investigated the rate of TTF-1 expression in lung metastases of extrathoracic adenocarcinomas and compared results of immunohistochemistry performed with different primary antibodies. Two different clones of antibodies (8G7G1/1 from Dako, SPT24 from Novocastra) raised against TTF-1 were used on 56 lung-metastatic malignant tumors, 41 from colorectal origin. A series of primary colorectal (90 cases) and primary pulmonary adenocarcinomas (86 cases) were also investigated. Four of 41 (10%) lung metastases of colorectal adenocarcinomas displayed a nuclear staining for TTF-1 with SPT24 clone. Three of the four positive cases displayed similar nuclear staining in primary and/or other extrathoracic metastatic sites as well as four of 90 (5%) primary colorectal adenocarcinomas, ruling out the role of lung microenvironment. None of them was positive with 8G7G1/1 clone. Sensitivity between two sets of antibodies was compared in 86 primary pulmonary adenocarcinomas. Nuclear staining was detected in 72 cases (84%) with Novocastra's antibody and 56 cases (65%) with Dako's. Significant discordance was observed (P< 0.01). These results suggest that the diagnostic virtue of TTF-1 detection depends on the used antibody's clone. The SPT24 clone seems to have a stronger affinity for TTF-1 protein but may lead to a few positive colorectal adenocarcinomas.
机译:甲状腺转录因子-1(TTF-1)被认为是鉴别诊断的可靠标志物,可将肺原发性腺癌与胸外起源区分开。我们先前曾报道第一例大肠起源的肺转移,并伴有TTF-1的核表达。由于大多数先前的研究是针对一系列胸外原发肿瘤进行的,因此我们提出了肺微环境在TTF-1表达中可能发挥作用的问题。我们调查了胸外腺癌肺转移中TTF-1表达的速率,并比较了用不同的一抗进行的免疫组织化学结果。针对TTF-1产生的两种不同的抗体克隆(来自Dako的8G7G1 / 1,来自Novocastra的SPT24)被用于56例肺转移性恶性肿瘤,其中41例来自结直肠。还研究了一系列原发性大肠癌(90例)和原发性肺腺癌(86例)。大肠腺癌的41个(10%)肺转移中有四个显示了SPT24克隆对TTF-1的核染色。四例阳性病例中的三例在原发和/或其他胸外转移部位显示相似的核染色,以及90例(5%)原发性结肠直肠腺癌中的四例,排除了肺微环境的作用。他们都没有对8G7G1 / 1克隆呈阳性。在86例原发性肺腺癌中比较了两组抗体之间的敏感性。用Novocastra抗体检出72例(84%)核染色,用Dako检出56例(65%)。观察到显着不一致(P <0.01)。这些结果表明,TTF-1检测的诊断价值取决于所用抗体的克隆。 SPT24克隆似乎对TTF-1蛋白具有更强的亲和力,但可能导致一些阳性的结直肠腺癌。

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