BRM270 suppresses cervical cancer stem cell characteristics and progression by inhibiting SOX2

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dc.contributor.authorN Chandimali-
dc.contributor.authorH N Sun-
dc.contributor.authorY H Park-
dc.contributor.authorTaeho Kwon-
dc.date.accessioned2020-09-24T03:03:19Z-
dc.date.available2020-09-24T03:03:19Z-
dc.date.issued2020-
dc.identifier.issn0258-851X-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/22622-
dc.description.abstractBackground/Aim: Cervical cancer is one of the leading causes of cancer death in women worldwide. BRM270 (BRMLife) has therapeutic potential for cancer treatment owing to its ability to inhibit cell proliferation, and expression of cluster of differentiation (CD) 133 in CD133+ cancer cells. This study was designed to evaluate the therapeutic effects of plant extract formulation BRM270 against cervical cancer progression. Materials and Methods: The expression of sex-determining region Y-box 2 (SOX2) was tested in four different cervical cancer cell lines, HeLA, SiHa, Caski and C33A. SOX2-expressing SiHa and C33A cell lines were selected for further experiments on the in vitro and in vivo effects of BRM270 on cervical cancer progression using western blotting, flow cytometry, sphere-formation assay, magnetic-activated cell sorting of CD133+ cervical cancer cells, and xenografts in female athymic BALB/c nude mice. Results: In the present study, in cervical cancer stem cells (CSCs), we found that BRM270 inhibited expression of SOX2, which is associated with cervical cancer initiation and metastasis. BRM270 also inhibited CD133 expression and induced apoptosis of CSCs and suppressed CD133+ CSC proliferation and sphere formation in vitro as well as SiHa and C33A cell xenograft tumor growth in vivo. This was accompanied by down-regulation of markers of epithelial-to-mesenchymal transition. Conclusion: BRM270 might be an effective agent for cervical cancer treatment. ⓒ 2020 International Institute of Anticancer Research.-
dc.publisherInt Inst Anticancer Research-
dc.titleBRM270 suppresses cervical cancer stem cell characteristics and progression by inhibiting SOX2-
dc.title.alternativeBRM270 suppresses cervical cancer stem cell characteristics and progression by inhibiting SOX2-
dc.typeArticle-
dc.citation.titlein Vivo-
dc.citation.number0-
dc.citation.endPage1094-
dc.citation.startPage1085-
dc.citation.volume34-
dc.contributor.affiliatedAuthorTaeho Kwon-
dc.contributor.alternativeNameChandimali-
dc.contributor.alternativeNameSun-
dc.contributor.alternativeName박양호-
dc.contributor.alternativeName권태호-
dc.identifier.bibliographicCitationin Vivo, vol. 34, pp. 1085-1094-
dc.identifier.doi10.21873/invivo.11879-
dc.subject.keywordBRM270-
dc.subject.keywordCancer stem cells-
dc.subject.keywordCervical cancer-
dc.subject.keywordEpithelial-to-mesenchymal transition-
dc.subject.keywordSOX2-
dc.subject.localBRM270-
dc.subject.localcancer stem cell-
dc.subject.localCancer stem cell (CSC)-
dc.subject.localCancer stem cell-
dc.subject.localCancer stem cells-
dc.subject.localCancer Stem Cells-
dc.subject.localCervical caner-
dc.subject.localCervical Cancer-
dc.subject.localcervical cancer-
dc.subject.localCervical cancer-
dc.subject.localEpithelial-to-mesenchymal transition-
dc.subject.localSOX2-
dc.description.journalClassY-
Appears in Collections:
Jeonbuk Branch Institute > Primate Resources Center > 1. Journal Articles
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