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p16INK4a expression in idiopathic guttate hypomelanosis and subgroup analysis comparison with senile lentigo
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.advisor | 강희영 | - |
| dc.contributor.author | 김태형 | - |
| dc.date.accessioned | 2022-11-29T02:32:52Z | - |
| dc.date.available | 2022-11-29T02:32:52Z | - |
| dc.date.issued | 2021-08 | - |
| dc.identifier.other | 31188 | - |
| dc.identifier.uri | https://dspace.ajou.ac.kr/handle/2018.oak/20419 | - |
| dc.description | 학위논문(석사)--아주대학교 일반대학원 :의학과,2021. 8 | - |
| dc.description.tableofcontents | 제1장 INTRODUCTION 1 제2장 MATERIAL AND METHODS 2 제1절 Patients 2 제2절 Stain and immunohistochemistry 2 제3절 Imaging analysis 2 제4절 Cell counting 3 제5절 Statistical analysis 4 제6절 Ethics declaration 4 제3장 RESULTS 5 제4장 DISCUSSION 15 제5장 CONCLUSION 18 제6장 REFERENCES 19 | - |
| dc.language.iso | eng | - |
| dc.publisher | The Graduate School, Ajou University | - |
| dc.rights | 아주대학교 논문은 저작권에 의해 보호받습니다. | - |
| dc.title | p16INK4a expression in idiopathic guttate hypomelanosis and subgroup analysis comparison with senile lentigo | - |
| dc.type | Thesis | - |
| dc.contributor.affiliation | 아주대학교 일반대학원 | - |
| dc.contributor.alternativeName | Tae Hyung Kim | - |
| dc.contributor.department | 일반대학원 의학과 | - |
| dc.date.awarded | 2021. 8 | - |
| dc.description.degree | Master | - |
| dc.identifier.localId | 1227967 | - |
| dc.identifier.uci | I804:41038-000000031188 | - |
| dc.identifier.url | https://dcoll.ajou.ac.kr/dcollection/common/orgView/000000031188 | - |
| dc.subject.keyword | idiopathic guttate hypomelanosis | - |
| dc.subject.keyword | melanocytes | - |
| dc.subject.keyword | senescence | - |
| dc.subject.keyword | senile lentigo | - |
| dc.description.alternativeAbstract | Background: The role of the senescent cells in pigmentary disorders such as melasma, senile lentigo, and vitiligo has been studied. However, the status of cellular senescence in idiopathic guttate hypomelanosis (IGH) in vivo has not been proved. Objective: We investigated p16INK4a positivity in paired normal and lesional skin in the IGH and senile lentigo patients to evaluate cellular senescence. Materials and methods: Fiftyeight patients with IGH and 5 patients with senile lentigo were enrolled. Immunohistochemical stain using p16INK4a and MART-1 was performed and the p16INK4a positive melanocytes and fibroblasts were counted. The IGH skins were classified by sun-exposed and unexposed skin; 44 were sun exposed skin such as face, neck, arm, and legs, and 14 were unexposed skin of trunk. Five patients with senile lentigo were biopsied in face. Results: Expression of p16INK4a on melanocytes and fibroblasts showed age-dependent increase in both normal and lesion skins. There were significant increase in the number of p16INK4a positive melanocytes in the lesion compared to the normal skin (mean ± SD, 12.3±23.9 vs 3.4±6.6 per 100 melanocytes, p=0.005). Subgroup analysis of sun exposed group revealed that there were more p16INK4a positive melanocytes in lesion than the normal skin (15.3±26.4 vs 4.5±7.3 per 100 melanocytes, p=0.01). Whereas, there was no statistically significant difference p16INK4a melanocytes in unexposed skin. Conclusion: p16INK4a positive melanocytes were observed in the sun-exposed skin by age dependent manner. The number of p16INK4a positive melanocytes was increased in the lesional skin of IGH, suggesting a role of senescent melanocytes in the development of IGH. Further study in the role of p16INK4a melanocytes on regulation of skin pigmentation would be necessary. | - |
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- Graduate School of Ajou University > Department of Medicine > 3. Theses(Master)
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