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dc.contributor.author조용우-
dc.date.accessioned2019-11-26T06:52:49Z-
dc.date.available2019-11-26T06:52:49Z-
dc.date.issued2019-05-
dc.identifier.citationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v. 512, No. 3, Page. 511-516en_US
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0006291X19304553-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/114707-
dc.description.abstractCancer stem cells (CSCs) are a small population of cells with stem cell-like properties found in tumors. CSCs are closely associated with tumor heterogeneity, which influences tumor progress, metastasis, and drug resistance. Here, we propose a concept to enhance efficacy of cancer therapy through CSC reprogramming into non-tumorigenic cells using stem cell -derived exosomes with osteoinductive potential. We hypothesized that exosomes derived from osteogenic differentiating human adipose-derived stem cells (0D-EX0s) contain specific cargos capable of inducing osteogenic differentiation of CSCs. Quantitative RT-PCR analysis revealed that OD-EXO5 enhanced the expression of osteogenic-related genes, such as alkaline phosphatase (ALPL), osteocalcin (BGLAP), and runt-related transcription factor 2 (RUNX2). In addition, expression of drug-resistance genes such as ATP binding cassette (ABC) transporter, the breast cancer gene family (BCRA1 and BCRA2), and the ErbB gene family were significantly decreased in OD-EXO-treated CSCs. Our findings suggest that OD-EXOs function as a biochemical cue for CSC reprogramming and contribute to overcoming therapeutic resistance. (C) 2019 Elsevier Inc. All rights reserved.en_US
dc.description.sponsorshipThis research was supported by the Bio & Medical Technology Development Program of the National Research Foundation (NRF) funded by the Ministry of Science & Id (NRF-2018M3A9H1023767). This research was also supported by the Basic Science Research Program through a National Research Foundation of Korea grant funded by the Korean Government (MEST) (NRF-2017R1A5A1070259).en_US
dc.language.isoen_USen_US
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCEen_US
dc.subjectExosomesen_US
dc.subjectCancer stem cellsen_US
dc.subjectReprogrammingen_US
dc.subjectDrug resistanceen_US
dc.titleReprogramming of cancer stem cells into non-tumorigenic cells using stem cell exosomes for cancer therapyen_US
dc.typeArticleen_US
dc.relation.no3-
dc.relation.volume512-
dc.identifier.doi10.1016/j.bbrc.2019.03.072-
dc.relation.page511-516-
dc.relation.journalBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.contributor.googleauthorLee, Kyoung Soo-
dc.contributor.googleauthorChoi, Ji Suk-
dc.contributor.googleauthorCho, Yong Woo-
dc.relation.code2019001376-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF ENGINEERING SCIENCES[E]-
dc.sector.departmentDEPARTMENT OF MATERIALS SCIENCE AND CHEMICAL ENGINEERING-
dc.identifier.pidywcho7-
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COLLEGE OF ENGINEERING SCIENCES[E](공학대학) > MATERIALS SCIENCE AND CHEMICAL ENGINEERING(재료화학공학과) > Articles
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