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APE1 细胞质定位在人上皮性卵巢癌中的预后意义。

Prognostic significance of APE1 cytoplasmic localization in human epithelial ovarian cancer.

机构信息

Department of Gynecology and Obstetrics, Xijing Hospital, Fourth Military Medical University, 710032 Xi'an, People's Republic of China.

出版信息

Med Oncol. 2012 Jun;29(2):1265-71. doi: 10.1007/s12032-011-9931-y. Epub 2011 Apr 10.

Abstract

Cytoplasmic localization of apurinic/apyrimidinic endonuclease 1 (APE1) correlates with different tumorigenic processes and poor prognosis in several cancer types. However, rare investigation into the prognosis value of cytoplasmic localization of APE1 was provided in ovarian cancer. The present study examined for the first time the cytoplasmic localization of APE1 in epithelial ovarian cancer (EOC) by immunohistochemistry. The relationship between cytoplasmic localization of APE1 and clinicopathological parameters, as well as the correlation between cytoplasmic localization of APE1 and prognosis, was investigated. We found that cytoplasmic positivity was significantly higher in EOCs with low tumor differentiation (P = 0.002) and was significantly higher in advanced Federation International of Gynecology and Obstetrics (FIGO) stage (III + IV) patients compared to that in early FIGO stage (I + II) patients (40.7% vs. 11.8%; P = 0.002). No significant difference was observed in APE1 pattern referring to age, tumor size, family history, histological type, ascites, and lymphatic metastasis (P > 0.05). In addition, a lower survival rate was found in patients with cytoplasmic positive localization of APE1 compared to that in patients with cytoplasmic negative localization (P < 0.05). All these findings suggest that cytoplasmic localization of APE1 is associated with tumor progression and might be a valuable prognostic marker for EOC.

摘要

细胞质定位的脱嘌呤/脱嘧啶核酸内切酶 1(APE1)与几种癌症类型中的不同肿瘤发生过程和不良预后相关。然而,在卵巢癌中,对 APE1 细胞质定位的预后价值的研究很少。本研究首次通过免疫组织化学法检测上皮性卵巢癌(EOC)中 APE1 的细胞质定位。研究了 APE1 细胞质定位与临床病理参数之间的关系,以及 APE1 细胞质定位与预后之间的相关性。我们发现,在肿瘤分化程度低的 EOC 中,细胞质阳性率显著升高(P = 0.002),在晚期国际妇产科联合会(FIGO)分期(III+IV)患者中显著高于早期 FIGO 分期(I+II)患者(40.7% vs. 11.8%;P = 0.002)。APE1 模式与年龄、肿瘤大小、家族史、组织学类型、腹水和淋巴转移无关(P > 0.05)。此外,与细胞质阴性定位的患者相比,细胞质阳性定位的患者的生存率较低(P < 0.05)。所有这些发现表明,APE1 的细胞质定位与肿瘤进展有关,可能是 EOC 的一个有价值的预后标志物。

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