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Immune Response: A Missed Opportunity Between Vitamin D and Radiotherapy

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出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2021.646981

关键词

vitamin D; calcitriol; radiation; radiotherapy; immune response; tumor microenvironment

资金

  1. National Natural Science Foundation of China [82073331, 82003208]
  2. Jilin Province Science and Technology Development Plan Project [20200201599JC]
  3. Project of Science and Technology Department of Jilin Province [20190303151SF]

向作者/读者索取更多资源

Radiotherapy is a key treatment for various types of cancer, but enhancing its effectiveness remains a challenge. Radiation resistance is a major factor in cancer progression, making overcoming treatment resistance a top challenge for clinicians. Vitamin D can synergistically enhance the effects of radiotherapy, potentially contributing to improved treatment outcomes.
Radiotherapy (RT) is a mainstay treatment in several types of cancer and acts by mediating various forms of cancer cell death, although it is still a large challenge to enhance therapy efficacy. Radiation resistance represents the main cause of cancer progression, therefore, overcoming treatment resistance is now the greatest challenge for clinicians. Increasing evidence indicates that immune response plays a role in reprogramming the radiation-induced tumor microenvironment (TME). Intriguingly, radiation-induced immunosuppression possibly overwhelms the ability of immune system to ablate tumor cells. This induces an immune equilibrium, which, we hypothesize, is an opportunity for radiosensitizers to make actions. Vitamin D has been reported to act in synergistic with RT by potentiating antiproliferative effect induced by therapeutics. Additionally, vitamin D can also regulate the TME and may even lead to immunostimulation by blocking immunosuppression following radiation. Previous reviews have focused on vitamin D metabolism and epidemiological trials, however, the synergistic effect of vitamin D and existing therapies remains unknown. This review summarizes vitamin D mediated radiosensitization, radiation immunity, and vitamin D-regulated TME, which may contribute to more successful vitamin D-adjuvant radiotherapy.

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