| Literature DB >> 32446115 |
Yue-Tao Zhou1, Shuang-Shuang Li2, Min Ai2, Hong Chen2, Yi-Xiao Liu2, Bo-Yan Li2, Ye Zhao2, Wei-Wei Cai2, Bao Hou2, Lu-Lu Ni2, Fei Xu2, Li-Ying Qiu3.
Abstract
Cancer-related fatigue (CRF) is one of the most common and serious complications in cancer patients, which greatly reduces the quality of life. The mechanism induced fatigue may be diverse. In this study, we tried to investigate the effect of 1,25(OH)2D3, the active metabolite of vitamin D on CRF in Lewis lung cancer-bearing mice. Network pharmacological analysis, behavioral testing, western blotting, ELISA and flow cytometry were used. We found that there was an interaction between proteins related to the role of 1,25(OH)2D3 and CRF-related proteins. The results of animal model experiments showed that 1,25(OH)2D3 could mitigate the CRF behavior of tumor-bearing mice, and the treatment of 1,25(OH)2D3 reduced the levels of inflammatory factors, changed the tryptophan metabolism direction, and caused changes in immune cells. Collectively, 1,25(OH)2D3 might improve CRF in tumor-bearing mice by changing the direction of tryptophan metabolism and inflammatory factor levels. This study provided a possible solution for patients with clinical CRF.Entities:
Keywords: 1,25(OH)(2)D(3); Cancer-related fatigue; Network pharmacological analysis; Tumor-bearing mice
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Year: 2020 PMID: 32446115 DOI: 10.1016/j.biopha.2020.110256
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529