4.3 Article

Quercetin Prevents Radiation-Induced Oral Mucositis by Upregulating BMI-1

Journal

OXIDATIVE MEDICINE AND CELLULAR LONGEVITY
Volume 2021, Issue -, Pages -

Publisher

HINDAWI LTD
DOI: 10.1155/2021/2231680

Keywords

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Funding

  1. National Natural Science Foundation of China [81272493, 81472213]
  2. Health Commission of Zhejiang Province [2019ZD010, 2019ZD029]
  3. Natural Science Foundation of Zhejiang Province [LY17H220001]
  4. Science Technology Department of Zhejiang Province [LGF20H220001]
  5. Zhejiang Provincial Administration of Traditional Chinese Medicine [2021ZA088]
  6. Basic Public Welfare Research Program of Zhejiang Province [LGD19H160005]

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Quercetin can prevent radiation-induced oral mucositis by reducing oxidative stress, inflammation, and DNA damage. It also contributes to ulcer repair and wound healing by promoting cell proliferation and repair mechanisms.
Radiation-induced oral mucositis is a major adverse event of radiotherapy. Severe oral mucositis may cause unwanted interruption in radiotherapy and reduce long-term survival in cancer patients receiving radiotherapy, but until now, there have been no effective options for preventing radiation-induced oral mucositis. Quercetin is a flavonoid that is widely found in food species and has anti-inflammatory, antioxidant, and anticancer activities. In this study, we investigated a new role of quercetin in preventing radiation-induced oral mucositis. Quercetin exerted preventive effects against radiation-induced oral mucositis induced by single-dose (25 Gy) ionizing radiation or fractionated ionizing radiation (8 Gy x 3) in C57BL/6 mice and maintained the proliferation ability of basal epithelial cells. Quercetin pretreatment alleviated reactive oxygen species generation, NF-xB pathway activation, and downstream proinflammatory cytokine production and reduced DNA double-strand breaks and cellular senescence induced by ionizing radiation. Quercetin also upregulated BMI-1 expression in oral epithelial cells and promoted ulcer repair. In addition, quercetin exerted similar radioprotective effects in irradiated primary cultured normal human keratinocytes, reduced reactive oxygen species generation and proinflammatory cytokine release, and promoted DNA double-strand break repair and wound healing by upregulating the expression of BMI-1, which is a polycomb group protein. Thus, quercetin can block multiple pathological processes of radiation-induced oral mucositis by targeting BMI-1 and may be a potential treatment option for preventing radiation-induced oral mucositis.

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