Burstein D E, Reder I, Weiser K, Tong T, Pritsker A, Haber R S
Department of Pathology, and Derald H. Ruttenberg Cancer Center, Mount Sinai School of Medicine, New York, New York 10029, USA.
Mod Pathol. 1998 Apr;11(4):392-6.
Malignant cells exhibit increased rates of glycolysis and glucose uptake, and several types of cancer have been reported to overexpress the GLUT1 glucose transporter. The diagnosis of malignancy in body cavity effusions remains a dilemma in certain cases, despite recent progress in diagnostic immunocytochemistry. We used immunostaining to detect the facilitative glucose transporter, GLUT1, in cytologic preparations of body cavity effusions and washes. With the use of standard avidin-biotin immunostaining for GLUT1, we examined cell blocks of body cavity effusions or washings from 31 carcinomas, 1 lymphoma, and 25 benign effusions or washes. GLUT1 staining occurred in the malignant cell population in 29 (93.5%) of 31 carcinomatous effusions or washes. The characteristic staining pattern consisted of dense, linear staining of the plasma membrane, with accentuation at cell-cell borders, with or without cytoplasmic staining. Erythrocytes showed positive GLUT1 membrane staining, consistent with previous reports. Of 25 benign effusions, 20 were nonstaining (excepting erythrocytes), and 5 contained rare single mesothelial cells, with equivocal to very weak membrane staining. Staining of these cells was readily distinguishable from the characteristic strong staining of malignant cells, and these cells were easily distinguished from tumor cells by their benign morphologic characteristics. At least three of these latter five specimens were from patients with cirrhosis. In all of the other cases, mesothelial cells, histiocytes, and other inflammatory cells did not stain. These findings suggest that GLUT1 immunostaining could be useful in diagnostic cytopathology. The findings also suggest that enhanced glycolysis, which requires increased glucose transport, might be a survival adaptation for tumor cells in effusions, a significant number of which are hypoxic.
恶性细胞表现出糖酵解速率和葡萄糖摄取增加,并且据报道几种类型的癌症中葡萄糖转运蛋白1(GLUT1)过度表达。尽管诊断免疫细胞化学最近取得了进展,但体腔积液中恶性肿瘤的诊断在某些情况下仍然是一个难题。我们使用免疫染色在体腔积液和冲洗液的细胞学制剂中检测易化葡萄糖转运蛋白GLUT1。通过使用针对GLUT1的标准抗生物素蛋白-生物素免疫染色,我们检查了31例癌、1例淋巴瘤以及25例良性积液或冲洗液的体腔积液细胞块。在31例癌性积液或冲洗液中的29例(93.5%)的恶性细胞群体中出现了GLUT1染色。特征性染色模式包括质膜的密集线性染色,在细胞-细胞边界处增强,有或无细胞质染色。红细胞显示GLUT1膜染色阳性,与先前报道一致。在25例良性积液中,20例无染色(红细胞除外),5例含有罕见的单个间皮细胞,膜染色不明确至非常弱。这些细胞的染色很容易与恶性细胞的特征性强染色区分开来,并且这些细胞通过其良性形态特征很容易与肿瘤细胞区分开来。后五个标本中至少有三个来自肝硬化患者。在所有其他病例中,间皮细胞、组织细胞和其他炎症细胞均未染色。这些发现表明GLUT1免疫染色在诊断细胞病理学中可能有用。这些发现还表明,需要增加葡萄糖转运的糖酵解增强可能是积液中肿瘤细胞的一种生存适应,其中相当一部分处于缺氧状态。