Cited 33 times in
A novel combination treatment of armed oncolytic adenovirus expressing IL-12 and GM-CSF with radiotherapy in murine hepatocarcinoma
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 금웅섭 | - |
dc.contributor.author | 김원우 | - |
dc.contributor.author | 성진실 | - |
dc.contributor.author | 오해진 | - |
dc.contributor.author | 최경주 | - |
dc.date.accessioned | 2014-12-20T17:18:37Z | - |
dc.date.available | 2014-12-20T17:18:37Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 0449-3060 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/94357 | - |
dc.description.abstract | In this study, a novel combination treatment of armed oncolytic adenovirus expressing interleukin 12 (IL-12) and granulocyte-macrophage colony-stimulating factor (GM-CSF) with radiation was investigated for antitumor and antimetastatic effect in a murine hepatic cancer (HCa-I) model. Tumor bearing syngeneic mice were treated with radiation, armed oncolytic virus Ad-ΔE1Bmt7 (dB7) expressing both IL-12 and GM-CSF (armed dB7), or a combination of both. The adenovirus was administered by intratumoral injection 1 × 10(8) PFU per tumor in 50 µl of PBS four times every other day. Tumor response to treatment was determined by a tumor growth delay assay. Metastatic potential was evaluated by a lung metastasis model. To understand the underlying mechanism, the level of apoptosis was examined as well as the change in microvessel density and expression of immunological markers: CD4+, CD8+ and Cd11c. The combination of armed dB7 and radiation resulted in significant growth delay of murine hepatic cancer, HCa-1, with an enhancement factor of 4.3. The combination treatment also resulted in significant suppression of lung metastasis. Increase of apoptosis level as well as decrease of microvessel density was shown in the combination treatment, suggesting an underlying mechanism for the enhancement of antitumor effect. Expression of immunological markers: CD4+, CD8+ and Cd11c also increased in the combination treatment. This study showed that a novel combination treatment of radiotherapy with armed oncolytic adenovirus expressing IL-12 and GM-CSF was effective in suppressing primary tumor growth. | - |
dc.description.statementOfResponsibility | open | - |
dc.format.extent | 646~654 | - |
dc.relation.isPartOf | JOURNAL OF RADIATION RESEARCH | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Adenoviridae/genetics | - |
dc.subject.MESH | Adenoviridae/pathogenicity | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Apoptosis | - |
dc.subject.MESH | Combined Modality Therapy | - |
dc.subject.MESH | Dendritic Cells/immunology | - |
dc.subject.MESH | Dendritic Cells/pathology | - |
dc.subject.MESH | Granulocyte-Macrophage Colony-Stimulating Factor/genetics | - |
dc.subject.MESH | Interleukin-12/genetics | - |
dc.subject.MESH | Liver Neoplasms, Experimental/pathology | - |
dc.subject.MESH | Liver Neoplasms, Experimental/radiotherapy* | - |
dc.subject.MESH | Liver Neoplasms, Experimental/secondary | - |
dc.subject.MESH | Liver Neoplasms, Experimental/therapy* | - |
dc.subject.MESH | Lung Neoplasms/secondary | - |
dc.subject.MESH | Lymphocytes, Tumor-Infiltrating/immunology | - |
dc.subject.MESH | Lymphocytes, Tumor-Infiltrating/pathology | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Mice | - |
dc.subject.MESH | Mice, Inbred C3H | - |
dc.subject.MESH | OncolyticVirotherapy* | - |
dc.subject.MESH | OncolyticViruses/genetics | - |
dc.subject.MESH | OncolyticViruses/pathogenicity | - |
dc.title | A novel combination treatment of armed oncolytic adenovirus expressing IL-12 and GM-CSF with radiotherapy in murine hepatocarcinoma | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Radiation Oncology (방사선종양학) | - |
dc.contributor.googleauthor | Wonwoo KIM | - |
dc.contributor.googleauthor | Jinsil SEONG | - |
dc.contributor.googleauthor | Hae Jin OH | - |
dc.contributor.googleauthor | Woong Sub KOOM | - |
dc.contributor.googleauthor | Kyung-Joo CHOI | - |
dc.contributor.googleauthor | Chae-Ok YUN | - |
dc.identifier.doi | 10.1269/jrr.10185 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A00273 | - |
dc.contributor.localId | A00768 | - |
dc.contributor.localId | A01956 | - |
dc.contributor.localId | A02413 | - |
dc.contributor.localId | A04034 | - |
dc.relation.journalcode | J01727 | - |
dc.identifier.eissn | 1349-9157 | - |
dc.identifier.pmid | 21952320 | - |
dc.subject.keyword | Oncolytic adenovirus | - |
dc.subject.keyword | Interleukin 12 | - |
dc.subject.keyword | Granulocyte-macrophage colony-stimulating factor | - |
dc.subject.keyword | Radiation | - |
dc.subject.keyword | Apoptosis | - |
dc.contributor.alternativeName | Koom, Woong Sub | - |
dc.contributor.alternativeName | Kim, Won Woo | - |
dc.contributor.alternativeName | Seong, Jin Sil | - |
dc.contributor.alternativeName | Oh, Hae Jin | - |
dc.contributor.alternativeName | Choi, Kyung Ju | - |
dc.contributor.affiliatedAuthor | Koom, Woong Sub | - |
dc.contributor.affiliatedAuthor | Kim, Won Woo | - |
dc.contributor.affiliatedAuthor | Seong, Jin Sil | - |
dc.contributor.affiliatedAuthor | Oh, Hae Jin | - |
dc.contributor.affiliatedAuthor | Choi, Kyung Ju | - |
dc.rights.accessRights | free | - |
dc.citation.volume | 52 | - |
dc.citation.number | 5 | - |
dc.citation.startPage | 646 | - |
dc.citation.endPage | 654 | - |
dc.identifier.bibliographicCitation | JOURNAL OF RADIATION RESEARCH, Vol.52(5) : 646-654, 2011 | - |
dc.identifier.rimsid | 27569 | - |
dc.type.rims | ART | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.