Wang Kai, Guan Chenan, Fang Chenyan, Jin Xiaoxiao, Yu Junhui, Zhang Yuquan, Zheng Lingzhi
Department of Obstetrics and Gynecology, Taizhou Hospital of Zhejiang Province, Wenzhou Medical University, Linhai, Zhejiang 317000, P.R. China.
Department of Kidney Internal Medicine, Taizhou Hospital of Zhejiang Province, Wenzhou Medical University, Linhai, Zhejiang 317000, P.R. China.
Oncol Lett. 2018 Apr;15(4):4457-4462. doi: 10.3892/ol.2018.7899. Epub 2018 Jan 29.
Forkhead box (FOX) A1 is a member of the FOX family of transcription factors, which serve a function in numerous types of tumor. The present study assessed the potential role of FOXA1 in human epithelial ovarian carcinoma (EOC). Total RNA was isolated from 16 fresh-frozen EOC tumors with paired corresponding non-malignant ovarian epithelium tissues, and FOXA1 expression was analyzed using reverse transcription-quantitative polymerase chain reaction. Immunohistochemical analysis was performed to evaluate FOXA1 expression in 110 epithelial ovarian carcinoma tissue specimens (including 80 serous papillary adenocarcinoma, 9 clear cell carcinoma, 12 endometrioid adenocarcinoma, 5 mucinous carcinoma and 4 transitional cell carcinoma specimens), 24 benign ovarian tumor surface epithelium tissues and 10 normal ovarian tissue samples. The present study analyzed the association between FOXA1 expression and clinical characteristics in patients with EOC. The Kaplan-Meier method was used for survival analysis. The results of the present study revealed that FOXA1 mRNA expression was significantly increased in EOC tissues compared with paired normal ovarian samples (P=0.014). The immunohistochemical expression of FOXA1 in EOC tissues was associated with the FIGO grade, differentiation status and overall survival time (all P<0.05). Finally, the significance of FOXA1 expression in the prognosis of the patients was evaluated. The results of Kaplan-Meier survival curve revealed that high FOXA1 expression was associated with decreased overall survival time in the patients, relative to low FOXA1 expression (P=0.0132). In conclusion, FOXA1 is overexpressed in EOC and associated with clinicopathological features, including overall survival time. FOXA1 potentially represents a novel biomarker and therapeutic target for EOC.
叉头框(FOX)A1是转录因子FOX家族的成员之一,其在多种类型的肿瘤中发挥作用。本研究评估了FOXA1在人上皮性卵巢癌(EOC)中的潜在作用。从16例新鲜冷冻的EOC肿瘤及其配对的相应非恶性卵巢上皮组织中分离总RNA,并使用逆转录-定量聚合酶链反应分析FOXA1表达。进行免疫组织化学分析以评估110例上皮性卵巢癌组织标本(包括80例浆液性乳头状腺癌、9例透明细胞癌、12例子宫内膜样腺癌、5例黏液性癌和4例移行细胞癌标本)、24例良性卵巢肿瘤表面上皮组织和10例正常卵巢组织样本中FOXA1的表达。本研究分析了EOC患者中FOXA1表达与临床特征之间的关联。采用Kaplan-Meier法进行生存分析。本研究结果显示,与配对的正常卵巢样本相比,EOC组织中FOXA1 mRNA表达显著增加(P = 0.014)。EOC组织中FOXA1的免疫组织化学表达与国际妇产科联盟(FIGO)分级、分化状态和总生存时间相关(均P < 0.05)。最后,评估了FOXA1表达在患者预后中的意义。Kaplan-Meier生存曲线结果显示,与低FOXA1表达相比,高FOXA1表达与患者总生存时间缩短相关(P = 0.0132)。总之,FOXA1在EOC中过表达,并与包括总生存时间在内的临床病理特征相关。FOXA1可能是EOC的一种新型生物标志物和治疗靶点。