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

dc.author.wosidKozanoglu, Ilknur/AAE-1241-2021
dc.author.wosidCakmakoglu, Bedia/G-9683-2017
dc.author.wosidBireller, Sinem/S-9157-2017
dc.author.wosidErtugrul, Baris/AAB-7579-2020
dc.authoridKozanoglu, Ilknur/0000-0002-5268-1210
dc.authoridCakmakoglu, Bedia/0000-0001-7960-9131
dc.authoridBireller, Sinem/0000-0003-3465-1808
dc.authoridErtugrul, Baris/0000-0003-3878-1829
dc.authoridBaran, Yusuf/0000-0002-1056-4673
dc.contributor.authorIplik, Elif Sinem
dc.contributor.authorErtugrul, Baris
dc.contributor.authorKozanoglu, Ilknur
dc.contributor.authorBaran, Yusuf
dc.contributor.authorCakmakoglu, Bedia
dc.contributor.authorBaran, Yusuf
dc.date.accessioned2023-11-18T10:06:20Z
dc.date.available2023-11-18T10:06:20Z
dc.date.issued2018
dc.departmentIzmir Institute of Technology İYTEen_US
dc.department-temp[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, Turkeyen_US
dc.descriptionKozanoglu, 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/0000-0002-1056-4673en_US
dc.description.abstractObjective(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.sponsorshipIstanbul University Scientific Research Project [39247]en_US
dc.description.sponsorshipThis 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.citation8
dc.identifier.doi10.22038/IJBMS.2018.26152.6420
dc.identifier.endpage468en_US
dc.identifier.issn2008-3866
dc.identifier.issn2008-3874
dc.identifier.issue5en_US
dc.identifier.pmid29922425
dc.identifier.scopusqualityQ3
dc.identifier.startpage465en_US
dc.identifier.urihttps://doi.org/10.22038/IJBMS.2018.26152.6420
dc.identifier.urihttp://standard-demo.gcris.com/handle/123456789/6981
dc.identifier.volume21en_US
dc.identifier.wosWOS:000433360100004
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.opencitations.citationcount5
dc.plumx.mendeleyreaders8
dc.plumx.pubmedcitations5
dc.plumx.scopuscitations9
dc.publisherMashhad Univ Med Sciencesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectApoptosisen_US
dc.subjectColon canceren_US
dc.subjectStem cellsen_US
dc.subjectCell deathen_US
dc.titleAn answer to colon cancer treatment by mesenchymal stem cell originated from adipose tissueen_US
dc.typeArticleen_US
dc.wos.citedbyCount8
dspace.entity.typePublication
relation.isAuthorOfPublication284ecb77-30bf-4d4d-a1b9-c35c6e2c8434
relation.isAuthorOfPublication.latestForDiscovery284ecb77-30bf-4d4d-a1b9-c35c6e2c8434

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