THE EXPRESSION ANALYSIS OF SPECIFIC GENES IN OVARIAN CANCER

Ece GÜMÜŞOĞLU-ACAR, Berkcan DOĞAN, Mehmet Ulaş BİLİR, Tugce SENTURK-KİRMİZİTAS, Samet TOPUZ, Tuba GUNEL
{"title":"THE EXPRESSION ANALYSIS OF SPECIFIC GENES IN OVARIAN CANCER","authors":"Ece GÜMÜŞOĞLU-ACAR, Berkcan DOĞAN, Mehmet Ulaş BİLİR, Tugce SENTURK-KİRMİZİTAS, Samet TOPUZ, Tuba GUNEL","doi":"10.59312/ebshealth.1367196","DOIUrl":null,"url":null,"abstract":"Aim: Ovarian cancer (OC) is the most lethal gynecologic malignancy and frequently diagnosed at an advanced stage because of the inadequate number of biomarkers. Therefore, identification of OC specific biological markers is a vital step for diagnosis and treatment response. Our goal is to examine functional gene sets which are possibly markers for ovarian cancer and their expression profiles in OC patients. We also aim to determine the potential genes for therapeutic targets for OC patients. 
 Method: The expression levels of seven genes (FOS, FOSL2, JUN, MMP-2, MMP-9, TIMP-2, and VEGFA) were identified by qRT-PCR. The tumor-free control group consisted of total abdominal hysterectomy (n=1) and bilateral salpingo-oophorectomy (n=9) patients who underwent gynecologic procedures. High-grade serous OC epithelial samples (n=10) were used for the experiment group. 
 Results and Conclusions: According to the qRT-PCR data, there is an increased expression of FOS (p=0.0089), MMP-9 (p=0.0029), VEGFA (p=0.0434) and decreased expression of FOSL2 (p=0.0271), JUN (p=0.0041), TIMP-2 (p=0.0062). In conclusion, the results can indicate the new perspective for OC pathogenesis and treatment. For future studies, these genes can be used in personalized diagnosis and therapy of OC.","PeriodicalId":474982,"journal":{"name":"Doğu Karadeniz Sağlık Bilimleri Dergisi","volume":"4 8","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Doğu Karadeniz Sağlık Bilimleri Dergisi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.59312/ebshealth.1367196","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Aim: Ovarian cancer (OC) is the most lethal gynecologic malignancy and frequently diagnosed at an advanced stage because of the inadequate number of biomarkers. Therefore, identification of OC specific biological markers is a vital step for diagnosis and treatment response. Our goal is to examine functional gene sets which are possibly markers for ovarian cancer and their expression profiles in OC patients. We also aim to determine the potential genes for therapeutic targets for OC patients. Method: The expression levels of seven genes (FOS, FOSL2, JUN, MMP-2, MMP-9, TIMP-2, and VEGFA) were identified by qRT-PCR. The tumor-free control group consisted of total abdominal hysterectomy (n=1) and bilateral salpingo-oophorectomy (n=9) patients who underwent gynecologic procedures. High-grade serous OC epithelial samples (n=10) were used for the experiment group. Results and Conclusions: According to the qRT-PCR data, there is an increased expression of FOS (p=0.0089), MMP-9 (p=0.0029), VEGFA (p=0.0434) and decreased expression of FOSL2 (p=0.0271), JUN (p=0.0041), TIMP-2 (p=0.0062). In conclusion, the results can indicate the new perspective for OC pathogenesis and treatment. For future studies, these genes can be used in personalized diagnosis and therapy of OC.
卵巢癌特异性基因的表达分析
目的:卵巢癌(OC)是最致命的妇科恶性肿瘤,由于生物标志物数量不足,经常在晚期诊断。因此,识别卵巢癌特异性生物标志物是诊断和治疗反应的重要步骤。我们的目标是研究可能作为卵巢癌标志物的功能基因集及其在卵巢癌患者中的表达谱。我们还旨在确定卵巢癌患者治疗靶点的潜在基因。& # x0D;方法:采用qRT-PCR法检测7个基因(FOS、FOSL2、JUN、MMP-2、MMP-9、TIMP-2、VEGFA)的表达水平。无肿瘤对照组包括接受妇科手术的全腹子宫切除术(n=1)和双侧输卵管卵巢切除术(n=9)患者。实验组采用高级别浆液性OC上皮样本(n=10)。& # x0D;结果与结论:qRT-PCR数据显示,FOS (p=0.0089)、MMP-9 (p=0.0029)、VEGFA (p=0.0434)表达升高,FOSL2 (p=0.0271)、JUN (p=0.0041)、TIMP-2 (p=0.0062)表达降低。本研究结果可为卵巢癌的发病机制及治疗提供新的思路。在未来的研究中,这些基因可用于卵巢癌的个性化诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信