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Irradiation-induced localization of IL-12-expressing mesenchymal stem cells to enhance the curative effect in murine metastatic hepatoma

DC Field Value Language
dc.contributor.author성진실-
dc.contributor.author이은정-
dc.contributor.author양승현-
dc.date.accessioned2016-02-04T11:21:02Z-
dc.date.available2016-02-04T11:21:02Z-
dc.date.issued2015-
dc.identifier.issn0020-7136-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/140229-
dc.description.abstractIrradiation in conjunction with gene therapy is considered for efficient cancer treatment. Mesenchymal stem cells (MSCs), due to their irradiation-promotable tumor tropism, are ideal delivery vehicles for gene therapy. In this study, we investigated whether treatment with radiation and interleukin (IL)-12-expressing MSCs (MSCs/IL-12) exerts improved antitumor effects on murine metastatic hepatoma. HCa-I and Hepa 1-6 cells were utilized to generate heterotopic murine hepatoma models. Tumor-bearing mice were treated with irradiation or MSCs/IL-12 alone, or a combination. Monocyte chemoattractant protein-1 (MCP-1/CCL2) expression was assessed in irradiated hepatoma tissues to confirm a chemotactic effect. Combination treatment strategies were established and their therapeutic efficacies were evaluated by monitoring tumor growth, metastasis and survival rate. IL-12 expression was assessed and the apoptotic activity and immunological alterations in the tumor microenvironment were examined. MCP-1/CCL2 expression and localization of MSCs/IL-12 increased in the irradiated murine hepatoma cells. The antitumor effects, including suppression of pulmonary metastasis and survival rate improvements, were increased by the combination treatment with irradiation and MSCs/IL-12. IL-12 expression was increased in tumor cells, causing proliferation of cluster of differentiation 8(+) T-lymphocytes and natural killer cells. The apoptotic activity increased, indicating that the cytotoxicity of immune cells was involved in the antitumor effect of the combined treatment. Treatment with irradiation and MSCs/IL-12 showed effectiveness in treating murine metastatic hepatoma. IL-12-induced proliferation of immune cells played an important role in apoptosis of tumor cells. Our results suggest that treatment with irradiation and MSCs/IL-12 may be a useful strategy for enhancing antitumor activity in metastatic hepatoma.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnimals-
dc.subject.MESHApoptosis/genetics-
dc.subject.MESHApoptosis/radiation effects-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHChemokine CCL2/genetics-
dc.subject.MESHChemokine CCL2/metabolism-
dc.subject.MESHDisease Models, Animal-
dc.subject.MESHGene Expression Regulation, Neoplastic/radiation effects-
dc.subject.MESHGenetic Therapy-
dc.subject.MESHInterleukin-12/genetics*-
dc.subject.MESHInterleukin-12/metabolism-
dc.subject.MESHKiller Cells, Natural/immunology-
dc.subject.MESHKiller Cells, Natural/metabolism-
dc.subject.MESHLiver Neoplasms/genetics-
dc.subject.MESHLiver Neoplasms/pathology*-
dc.subject.MESHLiver Neoplasms/therapy-
dc.subject.MESHMale-
dc.subject.MESHMesenchymal Stem Cell Transplantation*-
dc.subject.MESHMesenchymal Stromal Cells/metabolism*-
dc.subject.MESHMesenchymal Stromal Cells/radiation effects*-
dc.subject.MESHMice-
dc.subject.MESHMonocytes/metabolism-
dc.subject.MESHMonocytes/radiation effects-
dc.subject.MESHNeoplasm Metastasis-
dc.subject.MESHRadiation, Ionizing*-
dc.subject.MESHRadiotherapy-
dc.subject.MESHT-Lymphocyte Subsets/immunology-
dc.subject.MESHT-Lymphocyte Subsets/metabolism-
dc.titleIrradiation-induced localization of IL-12-expressing mesenchymal stem cells to enhance the curative effect in murine metastatic hepatoma-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Radiation Oncology (방사선종양학)-
dc.contributor.googleauthorKeun-Yeong Jeong-
dc.contributor.googleauthorEun-Jung Lee-
dc.contributor.googleauthorSu Jin Kim-
dc.contributor.googleauthorSeung-Hyun Yang-
dc.contributor.googleauthorYoung Chul Sung-
dc.contributor.googleauthorJinsil Seong-
dc.identifier.doi10.1002/ijc.29428-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA03047-
dc.contributor.localIdA01956-
dc.relation.journalcodeJ01092-
dc.identifier.eissn1097-0215-
dc.identifier.pmid25639194-
dc.identifier.urlhttp://onlinelibrary.wiley.com/doi/10.1002/ijc.29428/abstract-
dc.subject.keywordHCC-
dc.subject.keywordIL-12-
dc.subject.keywordgene therapy-
dc.subject.keywordirradiation-
dc.subject.keywordmesenchymal stem cell-
dc.subject.keywordmetastasis-
dc.contributor.alternativeNameSeong, Jin Sil-
dc.contributor.alternativeNameLee, Eun Jung-
dc.contributor.affiliatedAuthorLee, Eun Jung-
dc.contributor.affiliatedAuthorSeong, Jin Sil-
dc.rights.accessRightsnot free-
dc.citation.volume137-
dc.citation.startPage721-
dc.citation.endPage730-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF CANCER, Vol.137 : 721-730, 2015-
dc.identifier.rimsid50364-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Research Institute (부설연구소) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers

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