Evaluation of MicroRNA Expressions in Ovarian Cancer

husnu tore yavuzsen
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Abstract

com-Objectives: The present study aims to evaluate the relationship between microribonucleic acid (miRNA) and target gene expressions with clinical and histopathological data in ovarian cancer. Methods: We evaluated 96 archival samples of paraffin-embedded tissue. Some potentially significant miRNA and target gene expressions were evaluated in different histopathological characteristics. These were quantified using real-time–polymerase chain reaction (RT–PCR) in tumor and normal tissue. In miRNA expressions, twofold changes are accepted as significant. Results: According to histopathological groups, 38 (39.6%) were endometroid adenocarcinoma, 11 (11.5%) were borderline serous, 29 (30.2%) were serous, and 18 (18.8%) were mucinous carcinoma. When evaluated according to their stages, 26 (27.1%) patients were stage 1A/1B. A relationship was found between miR200a and miR200c and histopathologic groups, between miR141 and estrogen receptors, between CXCL1 and survival status, and between KEAP1 and ki67. Additionally, miR200a in endometrial and miR200c in mucinous adenocarcinoma were overexpressed. When the relationship between all miRNAs and histopathological groups was evaluated, a significant change was found only in miR200c expression. It was significantly higher in serous than endometrial tumors and significantly higher in mucinous than endometroid tumors. Conclusion: These suggested that miR200a and 200c expressions might be useful for the evaluation of histopathological subgroups of ovarian cancer.
卵巢癌中MicroRNA表达的评价
目的:本研究旨在探讨卵巢癌中miRNA和靶基因表达与临床和组织病理学的关系。方法:对96份石蜡包埋组织档案标本进行评价。在不同的组织病理特征中评估一些潜在的显著miRNA和靶基因表达。在肿瘤和正常组织中使用实时聚合酶链反应(RT-PCR)进行定量。在miRNA表达中,双重变化被认为是显著的。结果:按组织病理学分组,子宫内膜样腺癌38例(39.6%),交界性浆液癌11例(11.5%),浆液癌29例(30.2%),黏液癌18例(18.8%)。根据分期进行评估时,26例(27.1%)患者为1A/1B期。miR200a和miR200c与组织病理组、miR141与雌激素受体、CXCL1与生存状态、KEAP1与ki67之间存在相关性。此外,子宫内膜miR200a和粘液腺癌miR200c过表达。当评估所有mirna与组织病理组之间的关系时,发现只有miR200c表达有显著变化。浆液性肿瘤明显高于子宫内膜瘤,黏液性肿瘤明显高于子宫内膜瘤。结论:miR200a和200c的表达可用于卵巢癌组织病理亚组的评估。
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CiteScore
5.60
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