Department of Immunology, Shandong University School of Medicine, Jinan, Shandong 250012, PR China.
Oncol Rep. 2011 Feb;25(2):353-8. doi: 10.3892/or.2010.1103. Epub 2010 Dec 13.
Programmed cell death 5 (PDCD5) is a novel apoptosis-promoting protein. Although the decreased expression of PDCD5 has been recently found in a few types of human tumors, the status and significance of PDCD5 in ovarian cancer has not been evaluated. In the present study, we detected PDCD5 expression in 20 normal human ovaries and 26 serous cystadenomas and 41 serous cystadenocarcinomas by RT-PCR, Western blotting and immunohistochemistry, and analyzed the relationship between PDCD5 expression and clinicopathological data or patient survival. PDCD5 was expressed in all normal ovaries and serous cystadenomas, 80% (16/20) of normal ovarian tissues and 76.9% (20/26) of serous cystadenomas with moderate or strong PDCD5 protein expression. In contrast, 22% (9/41) of serous cystadenocarcinomas had no detectable PDCD5 protein expression and 46.3% (19/41) exhibited weak PDCD5 expression. The overall expression of PDCD5 in serous cystadenocarcinoma was significantly lower compared with normal ovarian tissues or serous cystadenomas (p<0.01). Furthermore, lost or decreased PDCD5 expression in serous cystadenocarcinomas was associated significantly with FIGO stage (p<0.05) and poorer disease-specific survival of patients (p<0.05). In conclusion, our data suggest that lost or reduced PDCD5 expression may contribute to the pathogenesis of human serous cystadenocarcinomas.
程序性细胞死亡因子 5(PDCD5)是一种新型的促进细胞凋亡的蛋白。虽然最近在少数几种人类肿瘤中发现 PDCD5 的表达降低,但 PDCD5 在卵巢癌中的状态和意义尚未得到评估。在本研究中,我们通过 RT-PCR、Western blot 和免疫组织化学检测了 20 例正常卵巢、26 例浆液性囊腺瘤和 41 例浆液性囊腺癌中 PDCD5 的表达,并分析了 PDCD5 表达与临床病理数据或患者生存的关系。PDCD5 在所有正常卵巢和浆液性囊腺瘤中均有表达,80%(16/20)的正常卵巢组织和 76.9%(20/26)的浆液性囊腺瘤中 PDCD5 蛋白表达为中度或强阳性。相比之下,41 例浆液性囊腺癌中有 22%(9/41)无可检测的 PDCD5 蛋白表达,46.3%(19/41)表达弱 PDCD5。浆液性囊腺癌中 PDCD5 的总体表达明显低于正常卵巢组织或浆液性囊腺瘤(p<0.01)。此外,浆液性囊腺癌中 PDCD5 的缺失或减少与 FIGO 分期(p<0.05)和患者疾病特异性生存率降低显著相关(p<0.05)。综上所述,我们的数据表明,PDCD5 的缺失或减少可能有助于人类浆液性囊腺癌的发病机制。