Kim Jo-Heon, Choi Yoo Duk, Lee Ji Shin, Lee Jae Hyuk, Nam Jong Hee, Choi Chan
Department of Pathology, Chonnam National University Medical School and Hospital, Gwangju, Republic of Korea.
Acta Cytol. 2010 May-Jun;54(3):277-82. doi: 10.1159/000325035.
To evaluate the usefulness of thyroid transcription factor-1 (TTF-1) and CDX-2 in determining the primary tumor site of metastatic adenocarcinomas (ACs) in serous effusions.
Cell blocks were constructed from cells in metastatic AC effusion fluids (n = 97) that had been previously stained with a panel of antibodies against MOC-31, D2-40 and calretinin. Primary tumor sites included the lungs (n = 52), ovaries (n = 6), pancreas (n = 4), breasts (n = 3), bile duct (n = 2) and gastrointestinal (GI) tract (30), including stomach (n = 28) and colon (n = 2). Primary sites were determined by tissue confirmation of the original tumor or review of the clinical charts. Immunocytochemical staining was performed with antibodies against TTF-1 and CDX-2.
The lung ACs showed TTF-1 positivity in 58% (30/52) of cases. All nonpulmonary ACs lacked TTF-1 staining. Among the 30 GI ACs, 9 (30%) (7 from the stomach and 2 from the colon) showed CDX-2 positivity. All non-GI ACs lacked CDX-2 staining. Specificities and positive predictive values for TTF-1 and CDX-2 equaled 100% for metastatic pulmonary and GI ACs, respectively.
Our results suggested that TTF-1 and CDX-2 are specific markers to separate metastatic pulmonary and GI ACs, respectively, from other metastatic ACs in serous effusions. However, sensitivity values of these markers were low.
评估甲状腺转录因子-1(TTF-1)和尾型同源盒转录因子2(CDX-2)在确定浆液性积液中转移性腺癌(AC)原发肿瘤部位的作用。
从转移性AC积液(n = 97)中的细胞构建细胞块,这些积液先前已用一组抗MOC-31、D2-40和钙视网膜蛋白的抗体染色。原发肿瘤部位包括肺(n = 52)、卵巢(n = 6)、胰腺(n = 4)、乳腺(n = 3)、胆管(n = 2)和胃肠道(GI)(30例),包括胃(n = 28)和结肠(n = 2)。通过对原发肿瘤的组织确认或临床病历回顾确定原发部位。用抗TTF-1和CDX-2的抗体进行免疫细胞化学染色。
肺AC病例中58%(30/52)显示TTF-1阳性。所有非肺AC均无TTF-1染色。在30例GI AC中,9例(30%)(7例来自胃,2例来自结肠)显示CDX-2阳性。所有非GI AC均无CDX-2染色。TTF-1和CDX-2对转移性肺和GI AC的特异性和阳性预测值分别为100%。
我们的结果表明,TTF-1和CDX-2分别是区分浆液性积液中转移性肺和GI AC与其他转移性AC的特异性标志物。然而,这些标志物的敏感性值较低。