{"title":"LncRNA TTC28-AS1 promotes the progression of cervical cancer by targeting miR-377-3p","authors":"Nianhong Yang, Tingting Xia, Ying Huang","doi":"10.1111/jog.16331","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Aim</h3>\n \n <p>Cervical cancer (CC) is the fourth most common malignancy affecting women worldwide and has a poor prognosis. The aim of this study was to investigate the clinical significance and mechanism of TTC28-AS1 in CC.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>A total of 120 individuals suffering from CC were included in this study. RT-qPCR was used to detect the level of TTC28-AS1, and the prognostic value of TTC28-AS1 was analyzed by Kaplan–Meier curve and Cox regression analyses. Dual-Luciferase reporter assay was used to verify the targeting relationship between TTC28-AS1 and miR-377-3p. The proliferative ability of CC cells was detected by CCK-8 kit. The migration and invasion of CC cells were detected by transwell system.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The expression level of TTC28-AS1 was elevated in patients with CC, serving as an indicator of unfavorable clinical outcome. TTC28-AS1 may promote the proliferation, migration, and invasion of CC cells by targeting miR-377-3p.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>TTC28-AS1 has the potential to promote the malignant progression of CC by targeting miR-377-3p, thus emerging as a promising therapeutic target for the treatment of CC.</p>\n </section>\n </div>","PeriodicalId":16593,"journal":{"name":"Journal of Obstetrics and Gynaecology Research","volume":"51 6","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2025-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Obstetrics and Gynaecology Research","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jog.16331","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Aim
Cervical cancer (CC) is the fourth most common malignancy affecting women worldwide and has a poor prognosis. The aim of this study was to investigate the clinical significance and mechanism of TTC28-AS1 in CC.
Methods
A total of 120 individuals suffering from CC were included in this study. RT-qPCR was used to detect the level of TTC28-AS1, and the prognostic value of TTC28-AS1 was analyzed by Kaplan–Meier curve and Cox regression analyses. Dual-Luciferase reporter assay was used to verify the targeting relationship between TTC28-AS1 and miR-377-3p. The proliferative ability of CC cells was detected by CCK-8 kit. The migration and invasion of CC cells were detected by transwell system.
Results
The expression level of TTC28-AS1 was elevated in patients with CC, serving as an indicator of unfavorable clinical outcome. TTC28-AS1 may promote the proliferation, migration, and invasion of CC cells by targeting miR-377-3p.
Conclusions
TTC28-AS1 has the potential to promote the malignant progression of CC by targeting miR-377-3p, thus emerging as a promising therapeutic target for the treatment of CC.
期刊介绍:
The Journal of Obstetrics and Gynaecology Research is the official Journal of the Asia and Oceania Federation of Obstetrics and Gynecology and of the Japan Society of Obstetrics and Gynecology, and aims to provide a medium for the publication of articles in the fields of obstetrics and gynecology.
The Journal publishes original research articles, case reports, review articles and letters to the editor. The Journal will give publication priority to original research articles over case reports. Accepted papers become the exclusive licence of the Journal. Manuscripts are peer reviewed by at least two referees and/or Associate Editors expert in the field of the submitted paper.