Howell Viive M, Gill Anthony, Clarkson Adele, Nelson Anne E, Dunne Robert, Delbridge Leigh W, Robinson Bruce G, Teh Bin T, Gimm Oliver, Marsh Deborah J
Kolling Institute of Medical Research, University of Sydney, Royal North Shore Hospital, St. Leonards, New South Wales 2065, Australia.
J Clin Endocrinol Metab. 2009 Feb;94(2):434-41. doi: 10.1210/jc.2008-1740. Epub 2008 Nov 18.
Parafibromin, encoded by HRPT2, is the first marker with significant benefit in the diagnosis of parathyroid carcinoma. However, because parafibromin is only involved in up to 70% of parathyroid carcinomas and loss of parafibromin immunoreactivity may not be observed in all cases of HRPT2 mutation, a complementary marker is needed.
We sought to determine the efficacy of increased expression of protein gene product 9.5 (PGP9.5), encoded by ubiquitin carboxyl-terminal esterase L1 (UCHL1) as an additional marker to loss of parafibromin immunoreactivity for the diagnosis of parathyroid carcinoma.
In total, 146 parathyroid tumors and nine normal tissues were analyzed for the expression of parafibromin and PGP9.5 by immunohistochemistry and for UCHL1 by quantitative RT-PCR. These samples included six hyperparathyroidism-jaw tumor syndrome-related tumors and 24 sporadic carcinomas.
In tumors with evidence of malignancy, strong staining for PGP9.5 had a sensitivity of 78% for the detection of parathyroid carcinoma and/or HRPT2 mutation and a specificity of 100%. Complete lack of nuclear parafibromin staining had a sensitivity of 67% and a specificity of 100%. PGP9.5 was positive in a tumor with the HRPT2 mutation L64P that expressed parafibromin. Furthermore, UCHL1 was highly expressed in the carcinoma/hyperparathyroidism-jaw tumor syndrome group compared to normal (P < 0.05) and benign specimens (P < 0.001).
These results suggest that positive staining for PGP9.5 has utility as a marker for parathyroid malignancy, with a slightly superior sensitivity (P = 0.03) and similar high specificity to that of parafibromin.
由HRPT2编码的 parafibromin是甲状旁腺癌诊断中首个具有显著诊断价值的标志物。然而,由于parafibromin仅在高达70%的甲状旁腺癌中出现,且并非在所有HRPT2突变病例中都能观察到parafibromin免疫反应性缺失,因此需要一种互补性标志物。
我们试图确定由泛素羧基末端酯酶L1(UCHL1)编码的蛋白基因产物9.5(PGP9.5)表达增加作为parafibromin免疫反应性缺失的附加标志物用于甲状旁腺癌诊断的有效性。
通过免疫组织化学分析了总共146个甲状旁腺肿瘤和9个正常组织中parafibromin和PGP9.5的表达,并通过定量逆转录聚合酶链反应分析了UCHL1的表达。这些样本包括6个与甲状旁腺功能亢进-颌骨肿瘤综合征相关的肿瘤和24个散发性癌。
在有恶性证据的肿瘤中,PGP9.5强染色对甲状旁腺癌和/或HRPT2突变检测的敏感性为78%,特异性为100%。完全缺乏核parafibromin染色的敏感性为67%,特异性为100%。PGP9.5在一个携带HRPT2突变L64P且表达parafibromin的肿瘤中呈阳性。此外,与正常样本(P < 0.05)和良性样本(P < 0.001)相比,UCHL1在癌/甲状旁腺功能亢进-颌骨肿瘤综合征组中高表达。
这些结果表明,PGP9.5阳性染色可作为甲状旁腺恶性肿瘤的标志物,其敏感性略高(P = 0.03),特异性与parafibromin相似且较高。