Cited 7 times in
Focal exposure of limited lung volumes to high-dose irradiation down-regulated organ development-related functions and up-regulated the immune response in mouse pulmonary tissues.
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 조재호 | - |
dc.date.accessioned | 2017-02-24T03:19:08Z | - |
dc.date.available | 2017-02-24T03:19:08Z | - |
dc.date.issued | 2016 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/146309 | - |
dc.description.abstract | BACKGROUND: Despite the emergence of stereotactic body radiotherapy (SBRT) for treatment of medically inoperable early-stage non-small-cell lung cancer patients, the molecular effects of focal exposure of limited lung volumes to high-dose radiation have not been fully characterized. This study was designed to identify molecular changes induced by focal high-dose irradiation using a mouse model of SBRT. RESULTS: Central areas of the mouse left lung were focally-irradiated (3 mm in diameter) with a single high-dose of radiation (90 Gy). Temporal changes in gene expression in the irradiated and non-irradiated neighboring lung regions were analyzed by microarray. For comparison, the long-term effect (12 months) of 20 Gy radiation on a diffuse region of lung was also measured. The majority of genes were down-regulated in the focally-irradiated lung areas at 2 to 3 weeks after irradiation. This pattern of gene expression was clearly different than gene expression in the diffuse region of lungs exposed to low-dose radiation. Ontological and pathway analyses indicated these down-regulated genes were mainly associated with organ development. Although the number was small, genes that were up-regulated after focal irradiation were associated with immune-related functions. The temporal patterns of gene expression and the associated biological functions were also similar in non-irradiated neighboring lung regions, although statistical significance was greatly reduced when compared with those from focally-irradiated areas of the lung. From network analysis of temporally regulated genes, we identified inter-related modules associated with diverse functions, including organ development and the immune response, in both the focally-irradiated regions and non-irradiated neighboring lung regions. CONCLUSIONS: Focal exposure of lung tissue to high-dose radiation induced expression of genes associated with organ development and the immune response. This pattern of gene expression was also observed in non-irradiated neighboring areas of lung tissue, indicating a global lung response to focal high-dose irradiation. | - |
dc.description.statementOfResponsibility | open | - |
dc.format.extent | 1~21 | - |
dc.language | English | - |
dc.publisher | BioMed Central | - |
dc.relation.isPartOf | BMC GENETICS | - |
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 | Animals | - |
dc.subject.MESH | Dose-Response Relationship, Radiation | - |
dc.subject.MESH | Down-Regulation | - |
dc.subject.MESH | Gene Expression Profiling | - |
dc.subject.MESH | Gene Expression Regulation/radiation effects* | - |
dc.subject.MESH | Gene Ontology | - |
dc.subject.MESH | Immunity/genetics | - |
dc.subject.MESH | Immunity/radiation effects | - |
dc.subject.MESH | Lung/growth & development | - |
dc.subject.MESH | Lung/immunology | - |
dc.subject.MESH | Lung/radiation effects* | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Mice | - |
dc.subject.MESH | Pulmonary Fibrosis | - |
dc.subject.MESH | Radiosurgery | - |
dc.subject.MESH | Up-Regulation | - |
dc.title | Focal exposure of limited lung volumes to high-dose irradiation down-regulated organ development-related functions and up-regulated the immune response in mouse pulmonary tissues. | - |
dc.type | Article | - |
dc.publisher.location | England | - |
dc.contributor.college | College of Medicine | - |
dc.contributor.department | Dept. of Radiation Oncology | - |
dc.contributor.googleauthor | Bu-Yeo Kim | - |
dc.contributor.googleauthor | Hee Jin | - |
dc.contributor.googleauthor | Yoon-Jin Lee | - |
dc.contributor.googleauthor | Ga-Young Kang | - |
dc.contributor.googleauthor | Jaeho Cho | - |
dc.contributor.googleauthor | Yun-Sil Lee | - |
dc.identifier.doi | 10.1186/s12863-016-0338-9 | - |
dc.contributor.localId | A03901 | - |
dc.relation.journalcode | J02848 | - |
dc.identifier.eissn | 1471-2156 | - |
dc.identifier.pmid | 26818610 | - |
dc.subject.keyword | Stereotactic body radiotherapy | - |
dc.subject.keyword | Focal radiation | - |
dc.subject.keyword | Microarray | - |
dc.subject.keyword | Organ development | - |
dc.subject.keyword | Immune response | - |
dc.contributor.alternativeName | Cho, Jae Ho | - |
dc.contributor.affiliatedAuthor | Cho, Jae Ho | - |
dc.citation.volume | 17 | - |
dc.citation.number | 29 | - |
dc.citation.startPage | 1 | - |
dc.citation.endPage | 21 | - |
dc.identifier.bibliographicCitation | BMC GENETICS, Vol.17(29) : 1-21, 2016 | - |
dc.date.modified | 2017-02-24 | - |
dc.identifier.rimsid | 53053 | - |
dc.type.rims | ART | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.