Lagana Stephen M, Salomao Marcela, Remotti Helen E, Knisely A S, Moreira Roger K
Department of Pathology and Cell Biology, Columbia University/New York Presbyterian Hospital, New York, NY, USA.
Histopathology. 2015 Mar;66(4):598-602. doi: 10.1111/his.12601. Epub 2015 Jan 23.
Bile salt export pump (BSEP) is a transporter expressed exclusively at hepatic canaliculi and drives bile-salt efflux. Minimal data exist about BSEP expression in tumours. We hypothesized that BSEP immunohistochemistry would be specific for hepatocellular carcinoma (HCC).
Tissue microarrays, including 48 HCC, 41 cholangiocarcinomas and 24 metastatic tumours in liver, were immunostained for BSEP. Expression was compared with common markers of hepatocytic differentiation including CD10, hepatocyte paraffin-1 antigen (HepPar-1), carcinoembryonic antigen, arginase-1 (ARG) and glypican-3 (GPC-3). BSEP expression was assessed in normal tissues. Special attention was given to adrenal gland (normal and neoplasia). BSEP was easy to interpret and showed no background staining. Canalicular expression was seen in all normal livers, but not in other normal tissue. BSEP was 90% sensitive and 100% specific for HCC (canalicular in 33 of 43 positive cases). The sensitivity of ARG was slightly higher, but specificity was slightly lower (94% for both). HepPar-1 was 90% sensitive and 97% specific. CD10, polyclonal carcinoembryonic antigen (pCEA) and GPC-3 all had lower sensitivity (74, 81 and 54%, respectively).
In malignant tumours in the liver, BSEP marking was 100% specific and 90% sensitive for HCC. The specificity of BSEP for HCC obviates the need to identify a 'canalicular' pattern, which can limit the utility of other canalicular markers.
胆盐输出泵(BSEP)是一种仅在肝小管表达的转运蛋白,可驱动胆盐流出。关于BSEP在肿瘤中的表达数据极少。我们推测BSEP免疫组化对肝细胞癌(HCC)具有特异性。
对包含48例HCC、41例胆管癌和24例肝脏转移瘤的组织芯片进行BSEP免疫染色。将其表达与肝细胞分化的常见标志物进行比较,这些标志物包括CD10、肝细胞石蜡-1抗原(HepPar-1)、癌胚抗原、精氨酸酶-1(ARG)和磷脂酰肌醇蛋白聚糖-3(GPC-3)。在正常组织中评估BSEP表达。特别关注肾上腺(正常和肿瘤)。BSEP易于解读且无背景染色。在所有正常肝脏中可见胆小管表达,但在其他正常组织中未见。BSEP对HCC的敏感性为90%,特异性为100%(43例阳性病例中有33例呈胆小管表达)。ARG的敏感性略高,但特异性略低(两者均为94%)。HepPar-1的敏感性为90%,特异性为97%。CD10、多克隆癌胚抗原(pCEA)和GPC-3的敏感性均较低(分别为74%、81%和54%)。
在肝脏恶性肿瘤中,BSEP标记对HCC的特异性为100%,敏感性为90%。BSEP对HCC所具有的特异性使得无需识别“胆小管”模式,而这种模式可能会限制其他胆小管标志物的效用。