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Long non-coding RNA, steroid receptor RNA activator (SRA), induces tumor proliferation and invasion through the NOTCH pathway in cervical cancer cell lines

DC Field Value Language
dc.contributor.author김상운-
dc.contributor.author김영태-
dc.contributor.author어경진-
dc.contributor.author이상길-
dc.contributor.author이혜연-
dc.date.accessioned2018-07-20T08:33:48Z-
dc.date.available2018-07-20T08:33:48Z-
dc.date.issued2017-
dc.identifier.issn1021-335X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/161286-
dc.description.abstractContemporary research has focused on the function of long non-coding RNAs (lncRNAs) in carcinogenesis. However, the involvement of the lncRNA, steroid receptor RNA activator (SRA), in cervical carcinogenesis remains to be elucidated. In the present study, we investigated the bio-functional consequences of lncRNA SRA knockdown in vitro. To verify the role of lncRNA SRA in cell proliferation, migration, and invasion, lncRNA RNA interference was utilized to knock down lncRNA SRA expression in cervical cancer cell lines, resulting in our discovery that lncRNA SRA knockdown inhibited cell proliferation, cell migration and tumor invasion in the cervical cancer cell lines. Additionally, in vitro experiments using the lncRNA SRA-knockdown cervical cancer cell lines revealed that lncRNA SRA is a strong inducer and modulator of the expression of genes related to epithelial-mesenchymal transition and the NOTCH signaling pathway. In conclusion, our findings demonstrated that lncRNA SRA is highly correlated with cancer progression and cervical cancer cell proliferation and migration. Furthermore, these results indicate that lncRNA SRA may be a potential therapeutic target and prognostic marker for cervical malignancy.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherD.A. Spandidos-
dc.relation.isPartOfONCOLOGY REPORTS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleLong non-coding RNA, steroid receptor RNA activator (SRA), induces tumor proliferation and invasion through the NOTCH pathway in cervical cancer cell lines-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Obstetrics & Gynecology-
dc.contributor.googleauthorKyung Jin Eoh-
dc.contributor.googleauthorJiheum Paek-
dc.contributor.googleauthorSang Wun Kim-
dc.contributor.googleauthorHee Jung Kim-
dc.contributor.googleauthorHye Yeon Lee-
dc.contributor.googleauthorSang Kil Lee-
dc.contributor.googleauthorYoung Tae Kim-
dc.identifier.doi10.3892/or.2017.6023-
dc.contributor.localIdA00526-
dc.contributor.localIdA00729-
dc.contributor.localIdA04842-
dc.contributor.localIdA02812-
dc.contributor.localIdA03313-
dc.relation.journalcodeJ02419-
dc.identifier.eissn1791-2431-
dc.identifier.pmid29039612-
dc.contributor.alternativeNameKim, Sang Wun-
dc.contributor.alternativeNameKim, Young Tae-
dc.contributor.alternativeNameEoh, Kyung Jin-
dc.contributor.alternativeNameLee, Sang Kil-
dc.contributor.alternativeNameLee, Hye Yeon-
dc.contributor.affiliatedAuthorKim, Sang Wun-
dc.contributor.affiliatedAuthorKim, Young Tae-
dc.contributor.affiliatedAuthorEoh, Kyung Jin-
dc.contributor.affiliatedAuthorLee, Sang Kil-
dc.contributor.affiliatedAuthorLee, Hye Yeon-
dc.citation.volume38-
dc.citation.number6-
dc.citation.startPage3481-
dc.citation.endPage3488-
dc.identifier.bibliographicCitationONCOLOGY REPORTS, Vol.38(6) : 3481-3488, 2017-
dc.identifier.rimsid61208-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Anatomy (해부학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers

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