Barroeta J E, Baloch Z W, Lal P, Pasha T L, Zhang P J, LiVolsi V A
Department of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.
Endocr Pathol. 2006 Fall;17(3):225-34. doi: 10.1385/ep:17:3:225.
Several immunohistochemical markers have been used to aid in the diagnosis of follicular-derived lesions of the thyroid (FDLT). In this study we analyze the diagnostic efficacy of an immunopanel of antibodies to cytokeratin-19 (CK19), galectin-3 (GAL-3), HBME-1, anti-MAP kinase (ERK), ret-oncoprotein (RET), and p16 using a tissue microarray consisting of both benign and malignant FDLT.
The study cohort consisted of 90 cases of FDLT (53 benign, 37 malignant) embedded in a microarray and immunostained with antibodies to CK19, Gal-3, HMBE-1, ERK, RET, and p16. Staining was scored as positive when >25% of the lesional cells showed positive immunostaining.
HMBE-1 was expressed in 70% of malignant and 10% of benign FDLT (p value: <0.0001). CK19 and GAL-3 were positive in 70% and 73% of malignant lesions, respectively, and 34% of benign FDLT (p value 0.0005 and 0.0015, respectively). ERK was positive in 4% of the benign and 32% of the malignant cases (p value 0.0002). p16 was expressed in 2% and 46% of the benign and malignant lesions, respectively (p value 0.0001). RET positivity was identified in 15% of the benign lesions and 27% of the malignant cases (p value 0.0016).
HBME-1, ERK, and p16 were more specific for malignancy, whereas CK19 and GAL-3 stained benign lesions with a higher frequency and were not specific for malignant FDLT. RET-oncoprotein showed poor sensitivity and specificity.
几种免疫组化标志物已被用于辅助诊断甲状腺滤泡源性病变(FDLT)。在本研究中,我们使用包含良性和恶性FDLT的组织微阵列,分析了细胞角蛋白-19(CK19)、半乳糖凝集素-3(GAL-3)、HBME-1、抗丝裂原活化蛋白激酶(ERK)、原癌蛋白(RET)和p16抗体免疫组化面板的诊断效能。
研究队列包括90例嵌入微阵列的FDLT(53例良性,37例恶性),并用CK19、Gal-3、HMBE-1、ERK、RET和p16抗体进行免疫染色。当>25%的病变细胞显示阳性免疫染色时,染色被评为阳性。
HBME-1在70%的恶性FDLT和10%的良性FDLT中表达(p值:<0.0001)。CK19和GAL-3分别在70%和73%的恶性病变中呈阳性,在34%的良性FDLT中呈阳性(p值分别为0.0005和0.0015)。ERK在4%的良性病例和32%的恶性病例中呈阳性(p值0.0002)。p16分别在2%的良性病变和46%的恶性病变中表达(p值0.0001)。在15%的良性病变和27%的恶性病例中发现RET阳性(p值0.0016)。
HBME-1、ERK和p16对恶性肿瘤更具特异性,而CK19和GAL-3在良性病变中的染色频率更高,对恶性FDLT不具有特异性。原癌蛋白RET的敏感性和特异性较差。