Youn Bo Sung, Kim Dong-Su, Kim Jae Wook, Kim Young Tae, Kang Suki, Cho Nam Hoon
Department of Obstetric Gynecology, Kangnam CHA Hospital, Seoul, Korea.
Mod Pathol. 2008 Jul;21(7):885-92. doi: 10.1038/modpathol.2008.64. Epub 2008 Apr 11.
The nm23 gene is a reported metastasis suppressor gene. Recent studies have shown that its expression has tissue specificity. The role of nm23 in human ovarian cancer is still controversial. This study examines the prognostic significance of nm23 expression in patients with serous ovarian carcinoma. Following comparative proteomics in 13 fresh frozen ovarian serous cancer tissues with other histological types of ovarian cancers, validation was performed using immunohistochemistry on clinically well-designed 73 ovarian serous carcinoma microarray samples that were retrieved from ovarian cancer patients from 1990 to 2003. Statistical analysis of the results was performed using chi(2) test, Cox proportional regression, the Kaplan-Meier method and log-rank test. We found that the expression of nm23 inversely correlated with peritoneal seeding (P=0.009). However, strong nm23 expression was associated with mortality in patients with ovarian carcinoma in univariate analysis (P=0.04). Poor prognostic factors of disease-free survival included tumor residue more than 2 cm (P=0.02), bilaterality (P=0.01) and peritoneal seeding (P<0.01), whereas poor prognostic factors affecting overall survival included peritoneal seeding (P=0.05). In Kaplan-Meier analysis, strong nm23 immunoreactivity correlates with poor overall survival (P=0.04) but not with poor disease-free survival. In conclusion, overexpression of nm23 is independently associated with decreased overall survival in patients with ovarian carcinoma and also significantly correlates with mortality. Nm23 may have a biological function that leads to poor clinical outcomes in ovarian carcinoma.
nm23基因是一种已报道的转移抑制基因。最近的研究表明,其表达具有组织特异性。nm23在人类卵巢癌中的作用仍存在争议。本研究探讨nm23表达在浆液性卵巢癌患者中的预后意义。在对13例新鲜冷冻的卵巢浆液性癌组织与其他组织学类型的卵巢癌进行比较蛋白质组学研究后,对1990年至2003年从卵巢癌患者中获取的73例临床设计良好的卵巢浆液性癌微阵列样本进行免疫组织化学验证。使用卡方检验、Cox比例回归、Kaplan-Meier方法和对数秩检验对结果进行统计分析。我们发现nm23的表达与腹膜种植呈负相关(P=0.009)。然而,在单因素分析中,nm23的强表达与卵巢癌患者的死亡率相关(P=0.04)。无病生存的不良预后因素包括肿瘤残留超过2 cm(P=0.02)、双侧性(P=0.01)和腹膜种植(P<0.01),而影响总生存的不良预后因素包括腹膜种植(P=0.05)。在Kaplan-Meier分析中,nm23的强免疫反应性与总生存不良相关(P=0.04),但与无病生存不良无关。总之,nm23的过表达与卵巢癌患者总生存降低独立相关,且与死亡率也显著相关。Nm23可能具有导致卵巢癌临床结局不良的生物学功能。