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An answer to colon cancer treatment by mesenchymal stem cell originated from adipose tissue

dc.contributor.author Iplik, Elif Sinem
dc.contributor.author Ertugrul, Baris
dc.contributor.author Kozanoglu, Ilknur
dc.contributor.author Baran, Yusuf
dc.contributor.author Cakmakoglu, Bedia
dc.contributor.author Baran, Yusuf
dc.date.accessioned 2023-11-18T10:06:20Z
dc.date.available 2023-11-18T10:06:20Z
dc.date.issued 2018
dc.description Kozanoglu, Ilknur/0000-0002-5268-1210; Cakmakoglu, Bedia/0000-0001-7960-9131; Bireller, Sinem/0000-0003-3465-1808; Ertugrul, Baris/0000-0003-3878-1829; Baran, Yusuf/0000-0002-1056-4673 en_US
dc.description.abstract Objective(s): Colon cancer is risen up with its complex mechanism that directly impacts on its treatment as well as its common prevalence. Mesenchymal stem cells (MSCs) have been considered as a therapeutic candidate for conventional disease including cancer. In this research, we have focused on apoptotic effects of adipose tissue-derived MSCs in colon cancer. Materials and Methods: MSCs were obtained from adipose tissue and characterized by Flowcytometer using suitable antibodies. MSCs, HT-29, HCT-116, RKO and healthy cell line MRC5 were cultured by different seeding procedure. After cell viability assay, changes in caspase 3 enzyme activity and the level of phosphatidylserine were measured. Results: For cell viability assay, a 48 hr incubation period was chosen to seed all cells together. There was a 1.36-fold decrease in caspase 3 enzyme activity by co-treatment of RKO and MSCs in addition to 2.02-fold decrease in HT-29 and MSCs co-treatment, and 1.103-fold increase in HCT-116 and MSCs. The results demonstrated that HCT-116 led to the highest rate of apoptotic cell death (7.5%) compared with other cells. Conclusion: We suggest that MSCs might remain a new treatment option for cancer by its differentiation and repair capacity. en_US
dc.description.sponsorship Istanbul University Scientific Research Project [39247] en_US
dc.description.sponsorship This work was funded by Istanbul University Scientific Research Project number 39247. We would like to thank Mr David F. Chapman for editing the manuscript. en_US
dc.identifier.citation 8
dc.identifier.doi 10.22038/IJBMS.2018.26152.6420
dc.identifier.issn 2008-3866
dc.identifier.issn 2008-3874
dc.identifier.uri https://doi.org/10.22038/IJBMS.2018.26152.6420
dc.identifier.uri http://standard-demo.gcris.com/handle/123456789/6981
dc.language.iso en en_US
dc.publisher Mashhad Univ Med Sciences en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Apoptosis en_US
dc.subject Colon cancer en_US
dc.subject Stem cells en_US
dc.subject Cell death en_US
dc.title An answer to colon cancer treatment by mesenchymal stem cell originated from adipose tissue en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Kozanoglu, Ilknur/0000-0002-5268-1210
gdc.author.id Cakmakoglu, Bedia/0000-0001-7960-9131
gdc.author.id Bireller, Sinem/0000-0003-3465-1808
gdc.author.id Ertugrul, Baris/0000-0003-3878-1829
gdc.author.id Baran, Yusuf/0000-0002-1056-4673
gdc.description.department Izmir Institute of Technology İYTE en_US
gdc.description.departmenttemp [Iplik, Elif Sinem] Istanbul Yeni Yuzyil Univ, Fac Pharm, Dept Pharmaceut Microbiol, Istanbul, Turkey; [Ertugrul, Baris; Cakmakoglu, Bedia] Istanbul Univ, Aziz Sancar Inst Expt Med, Dept Mol Med, Istanbul, Turkey; [Kozanoglu, Ilknur] Baskent Univ, Dept Hematol, Adana, Turkey; [Baran, Yusuf] Abdullah Gul Univ, Fac Life & Nat Sci, Kayseri, Turkey; [Baran, Yusuf] Izmir Inst Technol, Dept Mol Biol & Genet, Izmir, Turkey en_US
gdc.description.issue 5 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.volume 21 en_US
gdc.description.wosquality Q3
gdc.identifier.pmid 29922425
gdc.identifier.wos WOS:000433360100004
gdc.opencitations.count 5
gdc.plumx.mendeley 8
gdc.plumx.pubmedcites 5
gdc.plumx.scopuscites 9
gdc.wos.citedbycount 8
relation.isAuthorOfPublication 284ecb77-30bf-4d4d-a1b9-c35c6e2c8434
relation.isAuthorOfPublication.latestForDiscovery 284ecb77-30bf-4d4d-a1b9-c35c6e2c8434

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