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Radiation-induced esophagitis in vivo and in vitro reveals that epidermal growth factor (EGF) is a potential candidate for therapeutic intervention strategy : 방사선유발 식도염의 in vivo, in vitro 모델에서 표피성장인자(epidermal growth factor)의 효능 연구

DC Field Value Language
dc.contributor.advisor김학재-
dc.contributor.author김경수-
dc.date.accessioned2017-07-14T01:36:37Z-
dc.date.available2017-07-14T01:36:37Z-
dc.date.issued2016-08-
dc.identifier.other000000136030-
dc.identifier.urihttps://hdl.handle.net/10371/122155-
dc.description학위논문 (박사)-- 서울대학교 대학원 : 의학과 방사선종양학과, 2016. 8. 김학재.-
dc.description.abstractPurpose: To establish and characterize radiation-induced esophagitis (RIE) in vivo and in vitro.
Materials and Methods: Fractionated thoracic irradiation at 0, 8, 12, or 15 Gy was given daily for 5 days to Balb/c or C57Bl/6 mice. Changes in the body weight gain and daily food intake were assessed. At the end of the study, we harvested the esophagus and examined: (i) histology by H&E staining
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dc.description.abstract(ii) immune cell infiltration and apoptosis by Fluorescent activated cell sorting (FACS)-
dc.description.abstract(iii) gene expression changes by qRT-PCR. Het-1A human esophageal epithelial cells were irradiated at 6 Gy, treated with recombinant human growth factors, and examined for gene expression changes, apoptosis, proliferation, and signal transduction pathways.
Results: We observed that irradiation at 12 Gy or 15 Gy per fraction produced a significant body weight reduction and decreased food intake in Balb/c mice, but not so much in C57Bl/6 mice. Further analyses of Balb/c mice irradiated at 12 Gy/fraction revealed an attenuated epithelium, inflamed mucosa, and increased number of infiltrating CD4+ helper T cells and apoptotic cells. Moreover we found that expressions of tissue inhibitor for metalloproteinase-1, plasminogen activator inhibitor-1, granulocyte macrophage-colony stimulating factor, vascular endothelial growth factor, and stromal-derived factor-1 were increased while epidermal growth factor (Egf) was decreased. Irradiated Het-1A cells similarly showed a significant decrease in EGF and connective tissue growth factor (CTGF) expression. Treatment of EGF but not CTGF partially protected Het-1A cells from radiation-induced apoptosis and revealed phosphorylation of EGFR, AKT and ERK signaling pathways.
Conclusions: We established a mouse model of RIE in Balb/c mice with 12 Gy × 5 fractions, which exhibited reduced body weight gain, food intake, and histopathologic features similar to human esophagitis. Decreased EGF expression in the irradiated esophagus suggests that EGF may be a potential therapeutic intervention strategy to treat RIE.
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dc.description.tableofcontentsIntroduction 1

Materials and Methods 4

Results 10

Discussion 24

References 30

국문 초록 38
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dc.formatapplication/pdf-
dc.format.extent964815 bytes-
dc.format.mediumapplication/pdf-
dc.language.isoko-
dc.publisher서울대학교 대학원-
dc.subjectRadiation-induced esophagitis-
dc.subjectmouse model-
dc.subjectepidermal growth factor-
dc.subject.ddc610-
dc.titleRadiation-induced esophagitis in vivo and in vitro reveals that epidermal growth factor (EGF) is a potential candidate for therapeutic intervention strategy-
dc.title.alternative방사선유발 식도염의 in vivo, in vitro 모델에서 표피성장인자(epidermal growth factor)의 효능 연구-
dc.typeThesis-
dc.contributor.AlternativeAuthorKyung Su Kim-
dc.description.degreeDoctor-
dc.citation.pages40-
dc.contributor.affiliation의과대학 의학과-
dc.date.awarded2016-08-
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