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急性放射治疗诱导的犬皮肤损伤后皮肤的组织学和分子生物学变化

Histological and Molecular Biological Changes in Canine Skin Following Acute Radiation Therapy-Induced Skin Injury.

作者信息

Lee Sang-Yun, Hwang Gunha, Choi Moonyeong, Jo Chan-Hee, Oh Seong-Ju, Jin Yeung Bae, Lee Won-Jae, Rho Gyu-Jin, Lee Hee Chun, Lee Sung-Lim, Hwang Tae Sung

机构信息

College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, Republic of Korea.

Yangsan S Animal Cancer Center, Yangsan 50638, Republic of Korea.

出版信息

Animals (Basel). 2024 Aug 29;14(17):2505. doi: 10.3390/ani14172505.

DOI:10.3390/ani14172505
PMID:39272290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11394491/
Abstract

Radiation therapy is a crucial cancer treatment, but it can damage healthy tissues, leading to side effects like skin injuries and molecular alterations. This study aimed to elucidate histological and molecular changes in canine skin post-radiation therapy (post-RT) over nine weeks, focusing on inflammation, stem cell activity, angiogenesis, keratinocyte regeneration, and apoptosis. Four male beagles received a cumulative radiation dose of 48 Gy, followed by clinical observations, histological examinations, and an RT-qPCR analysis of skin biopsies. Histological changes correlated with clinical recovery from inflammation. A post-RT analysis revealed a notable decrease in the mRNA levels of Oct4, Sox2, and Nanog from weeks 1 to 9. VEGF 188 levels initially saw a slight increase at week 1, but they had significantly declined by week 9. Both mRNA and protein levels of COX-2 and Keratin 10 significantly decreased over the 9 weeks following RT, although COX-2 expression surged in the first 2 weeks, and Keratin 10 levels increased at weeks 4 to 5 compared to normal skin. Apoptosis peaked at 2 weeks and diminished, nearing normal by 9 weeks. These findings offer insights into the mechanisms of radiation-induced skin injury and provide guidance for managing side effects in canine radiation therapy.

摘要

放射治疗是一种关键的癌症治疗方法,但它会损害健康组织,导致皮肤损伤和分子改变等副作用。本研究旨在阐明犬类皮肤在放射治疗(放疗后)九周内的组织学和分子变化,重点关注炎症、干细胞活性、血管生成、角质形成细胞再生和细胞凋亡。四只雄性比格犬接受了48 Gy的累积辐射剂量,随后进行临床观察、组织学检查以及皮肤活检的RT-qPCR分析。组织学变化与炎症的临床恢复相关。放疗后分析显示,从第1周到第9周,Oct4、Sox2和Nanog的mRNA水平显著下降。VEGF 188水平在第1周最初略有上升,但到第9周时显著下降。放疗后9周内,COX-2和角蛋白10的mRNA和蛋白水平均显著下降,尽管COX-2表达在最初2周激增,与正常皮肤相比,角蛋白10水平在第4至5周有所增加。细胞凋亡在第2周达到峰值,随后减少,到第9周接近正常水平。这些发现为辐射诱导的皮肤损伤机制提供了见解,并为犬类放射治疗中的副作用管理提供了指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95bd/11394491/0ace7a25f5ba/animals-14-02505-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95bd/11394491/893db0ddb3f6/animals-14-02505-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95bd/11394491/cfcf60cb7d1a/animals-14-02505-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95bd/11394491/42e6bbef1199/animals-14-02505-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95bd/11394491/ee0af9014c50/animals-14-02505-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95bd/11394491/0ace7a25f5ba/animals-14-02505-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95bd/11394491/893db0ddb3f6/animals-14-02505-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95bd/11394491/cfcf60cb7d1a/animals-14-02505-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95bd/11394491/42e6bbef1199/animals-14-02505-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95bd/11394491/ee0af9014c50/animals-14-02505-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95bd/11394491/0ace7a25f5ba/animals-14-02505-g005.jpg

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本文引用的文献

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2
Adipose-derived stem cells alleviate radiation-induced dermatitis by suppressing apoptosis and downregulating cathepsin F expression.脂肪来源的干细胞通过抑制细胞凋亡和下调组织蛋白酶 F 的表达来缓解放射性皮炎。
Stem Cell Res Ther. 2021 Aug 9;12(1):447. doi: 10.1186/s13287-021-02516-1.
3
Mast cell degranulation and vascular endothelial growth factor expression in mouse skin following ionizing irradiation.
电离辐射后小鼠皮肤中的肥大细胞脱颗粒和血管内皮生长因子表达。
J Radiat Res. 2021 Sep 13;62(5):856-860. doi: 10.1093/jrr/rrab067.
4
Regulated Necrotic Cell Death in Alternative Tumor Therapeutic Strategies.肿瘤替代治疗策略中的程序性坏死性细胞死亡
Cells. 2020 Dec 17;9(12):2709. doi: 10.3390/cells9122709.
5
Radiation Induces Pulmonary Fibrosis by Promoting the Fibrogenic Differentiation of Alveolar Stem Cells.辐射通过促进肺泡干细胞的纤维化分化诱导肺纤维化。
Stem Cells Int. 2020 Sep 29;2020:6312053. doi: 10.1155/2020/6312053. eCollection 2020.
6
Dynamical reorganization of the pluripotency transcription factors Oct4 and Sox2 during early differentiation of embryonic stem cells.胚胎干细胞早期分化过程中多能转录因子 Oct4 和 Sox2 的动态重组织。
Sci Rep. 2020 Mar 23;10(1):5195. doi: 10.1038/s41598-020-62235-0.
7
Keratin 6, 16 and 17-Critical Barrier Alarmin Molecules in Skin Wounds and Psoriasis.角蛋白 6、16 和 17——皮肤创伤和银屑病中的关键屏障警报素分子。
Cells. 2019 Aug 1;8(8):807. doi: 10.3390/cells8080807.
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J Cell Mol Med. 2019 May;23(5):3178-3189. doi: 10.1111/jcmm.14174. Epub 2019 Feb 28.
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