Histological and Molecular Biological Changes in Canine Skin Following Acute Radiation Therapy-Induced Skin Injury.
Sang-Yun LeeGunha HwangMoonyeong ChoiChan-Hee JoSeong-Ju OhYeung-Bae JinWon-Jae LeeGyu-Jin RhoHee-Chun LeeSung-Lim LeeTae Sung HwangPublished in: Animals : an open access journal from MDPI (2024)
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.
Keyphrases
- radiation therapy
- radiation induced
- wound healing
- soft tissue
- stem cells
- oxidative stress
- gestational age
- locally advanced
- endothelial cells
- poor prognosis
- randomized controlled trial
- cell death
- gene expression
- squamous cell carcinoma
- diabetic rats
- clinical trial
- intensive care unit
- study protocol
- preterm birth
- small molecule
- extracorporeal membrane oxygenation
- cell cycle arrest
- high glucose
- optical coherence tomography
- mesenchymal stem cells
- cancer stem cells
- embryonic stem cells
- placebo controlled