Tominaga Yoshihiro, Tsuzuki Toyonori, Matsuoka Susumu, Uno Nobuaki, Sato Tetsuhiko, Shimabukuro Syuichi, Goto Norihiko, Nagasaka Takaharu, Uchida Kazuharu
Department of Transplant and Endocrine Surgery, Nagoya Second Red Cross Hospital, 2-9 Myoken-cho, Showa-ku, Nagoya 4668650, Japan.
World J Surg. 2008 May;32(5):815-21. doi: 10.1007/s00268-007-9458-8.
Recently, somatic inactivating mutations in HRPT2 have been reported in the majority of sporadic parathyroid carcinoma in primary hyperparathyroidism (HPT). Parafibromin is a tumor suppressor protein encoded by HRPT2, and loss of nuclear expression of parafibromin was found in approximately 70% of the carcinoma. In secondary HPT due to chronic kidney disease (CKD), parathyroid carcinoma is very rare and whether HRPT2 plays a role in the carcinogenesis in these cases is not clear. We evaluated the expression of parafibromin in hemodialysis patients with distant metastatic parathyroid tumors.
Between June 1973 and December 2006, 2,142 patients underwent parathyroidectomy (PTx) for secondary HPT in our department. We encountered five (0.23%) patients with distant metastatic parathyroid tumors. We evaluated the immunohistochemistry for parafibromin in eight primary parathyroid glands removed from the neck at the initial operation and/or at reoperation and seven distant metastatic tumors resected at reoperation.
In only one lung metastatic parathyroid tumor, negative staining for parafibromin was detected. In the other three lung, two regional node, and one chest wall metastatic parathyroid tumor, parafibromin was strongly stained in the nuclei of the parathyroid cells. Among eight primary glands, except for one with weakly positive staining, the expression of parafibromin was detected diffusely and strongly.
We conclude that the inactivating mutations and/or allelic loss of the HRPT2 gene may not play a major role in parathyroid carcinogenesis in secondary HPT due to CKD, but in these cases cancer development may be associated with a heterogeneous genetic disorder.
最近,在大多数原发性甲状旁腺功能亢进症(HPT)的散发性甲状旁腺癌中已报道HRPT2存在体细胞失活突变。 parafibromin是由HRPT2编码的一种肿瘤抑制蛋白,在大约70%的癌组织中发现parafibromin的核表达缺失。在慢性肾脏病(CKD)所致的继发性HPT中,甲状旁腺癌非常罕见,尚不清楚HRPT2在这些病例的致癌过程中是否起作用。我们评估了远处转移性甲状旁腺肿瘤的血液透析患者中parafibromin的表达情况。
1973年6月至2006年12月期间,我们科室有2142例患者因继发性HPT接受了甲状旁腺切除术(PTx)。我们遇到了5例(0.23%)有远处转移性甲状旁腺肿瘤的患者。我们评估了在初次手术和/或再次手术时从颈部切除的8个原发性甲状旁腺以及在再次手术时切除的7个远处转移瘤中parafibromin的免疫组化情况。
仅在1例肺转移性甲状旁腺肿瘤中检测到parafibromin染色阴性。在其他3例肺、2例区域淋巴结和1例胸壁转移性甲状旁腺肿瘤中,parafibromin在甲状旁腺细胞的细胞核中呈强染色。在8个原发性腺体中,除1例弱阳性染色外,均弥漫性强表达parafibromin。
我们得出结论,HRPT2基因的失活突变和/或等位基因缺失可能在CKD所致继发性HPT的甲状旁腺癌发生中不起主要作用,但在这些病例中癌症发展可能与一种异质性遗传疾病有关。