Intragland Expression of the Shh Gene Alleviates Irradiation-Induced Salivary Gland Injury through Microvessel Protection and the Regulation of Oxidative Stress.
Meijun HuLiang HuTao YangBowen ZhouXuanhe FengZhipeng FanZhaochen ShanPublished in: Antioxidants (Basel, Switzerland) (2024)
Radiation-induced salivary gland injury (RISGI) is a common complication of radiotherapy in patients with head and neck cancer. Intragland expression of the Sonic Hedgehog (Shh) gene may partially rescue irradiation (IR)-induced hyposalivation by preserving salivary stem/progenitor cells and parasympathetic innervation, maintaining resident macrophages, and maintaining microvascular density. Previous studies have revealed that Ad-Rat Shh transduction through the salivary glands of miniature pigs can ameliorate oxidative stress-induced microvascular dysfunction after radiotherapy. Changes in the parotid salivary flow rate were analyzed, and the parotid tissue was collected at 5 and 20 weeks after IR. Changes in the Hedgehog pathway and vascular function-related markers (vascular endothelial growth factor (VEGF) and CD31) and oxidative stress-related markers were detected via immunohistochemistry, immunofluorescence, and Western blotting. A stable Shh-overexpressing cell line was generated from human umbilical vein endothelial cells (HUVECs) and exposed to 10 Gy X-ray irradiation, after which endothelial cell proliferation, senescence, apoptosis, and vascular function were evaluated. We found that intragland expression of the Shh gene efficiently alleviated IR-induced parotid gland injury in a miniature pig model. Our results indicate that the antioxidative stress and microvascular-protective effects of the Hh pathway are regulated by nuclear factor-erythroid 2-related factor 2 (Nrf2).
Keyphrases
- oxidative stress
- radiation induced
- endothelial cells
- diabetic rats
- high glucose
- vascular endothelial growth factor
- poor prognosis
- dna damage
- nuclear factor
- radiation therapy
- cell proliferation
- early stage
- copy number
- genome wide
- drug induced
- toll like receptor
- binding protein
- magnetic resonance imaging
- induced apoptosis
- long non coding rna
- gene expression
- dna methylation
- genome wide identification
- cell cycle
- heart rate variability
- magnetic resonance
- stress induced
- immune response
- computed tomography
- genome wide analysis