上皮性卵巢癌患者肿瘤叉头盒Q1升高,与肿瘤大小增大、国际妇产联合会分期相关,但总生存率较差

Cancer biotherapy & radiopharmaceuticals Pub Date : 2022-11-01 Epub Date: 2021-03-23 DOI:10.1089/cbr.2020.4444
Xiaoyi Wang, Xiaowu Zhu
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引用次数: 1

摘要

背景:叉头盒Q1 (FOXQ1)调控上皮性卵巢癌(EOC)细胞的增殖、迁移和侵袭;然而,其对EOC患者预后的影响尚不清楚。本研究通过免疫组化(IHC)染色和逆转录-定量聚合酶链反应(RT-qPCR)检测FOXQ1在EOC患者中的表达,分析其与EOC患者临床特征及预后的相关性。材料与方法:采用免疫组化染色法检测173例切除的EOC患者肿瘤及癌旁组织中FOXQ1蛋白水平,并采用半定量评分法进行评分;同时,采用RT-qPCR检测173例EOC患者(有新鲜冷冻组织)中105例肿瘤及癌旁组织中FOXQ1 mRNA水平。收集EOC患者的临床特征及生存资料。结果:肿瘤组织中FOXQ1蛋白(n = 173)和mRNA (n = 105)水平均高于癌旁组织(p = 0.005)和FIGO分期(p = 0.037),而EOC患者FOXQ1肿瘤mRNA水平仅与肿瘤大小呈正相关(p = 0.015);但与其他临床特征如组织学亚型、肿瘤分化、腹膜细胞学等无相关性(均p > 0.05)。此外,肿瘤中FOXQ1蛋白(p = 0.030)和mRNA (p = 0.011)水平均与EOC患者总生存期(OS)降低相关。结论:FOXQ1在肿瘤组织中表达升高,其高表达与EOC患者肿瘤大小增大、FIGO分期升高、OS恶化有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumor Forkhead Box Q1 Is Elevated, Correlates with Increased Tumor Size, International Federation of Gynecology and Obstetrics Stage but Worse Overall Survival in Epithelial Ovarian Cancer Patients.

Background: Forkhead box Q1 (FOXQ1) regulates epithelial ovarian cancer (EOC) cell proliferation, migration, and invasion; however, its prognostic effect in EOC patients is unclear. This study assessed FOXQ1 expression in EOC patients by immunohistochemical (IHC) staining and reverse transcription-quantitative polymerase chain reaction (RT-qPCR) and to analyze its correlation with EOC patients' clinical features and prognosis. Materials and Methods: FOXQ1 protein level in tumor and adjacent tissues from 173 EOC patients who underwent resection was detected by IHC staining and further scored by a semiquantitative scoring method; meanwhile, FOXQ1 mRNA level in tumor and adjacent tissues from 105 out of 173 EOC patients (whose fresh-frozen tissues were available) was detected by RT-qPCR. Besides, EOC patients' clinical features and survival data were collected. Results: Both FOXQ1 protein (n = 173) and mRNA (n = 105) levels were increased in tumor tissues compared with adjacent tissues (both p < 0.001) in EOC patients. Meanwhile, tumor FOXQ1 protein level was positively correlated with tumor size (p = 0.005) and International Federation of Gynecology and Obstetrics (FIGO) stage (p = 0.037), while FOXQ1 tumor mRNA level was only positively correlated with tumor size (p = 0.015) in EOC patients; however, they were not correlated with other clinical features such as histological subtypes, tumor differentiation, peritoneal cytology, and so on (all p > 0.05). Moreover, FOXQ1 protein (p = 0.030) and mRNA (p = 0.011) levels in tumors were both correlated with worse overall survival (OS) in EOC patients. Conclusion: FOXQ1 is elevated in tumor tissues, and its high tumor expression correlates with increased tumor size, elevated FIGO stage, and worse OS in EOC patients.

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