Filip-Psurska Beata, Zachary Honorata, Strzykalska Aleksandra, Wietrzyk Joanna
Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Rudolfa Weigla St. 12, 53-114 Wroclaw, Poland.
Cancers (Basel). 2022 Jul 27;14(15):3649. doi: 10.3390/cancers14153649.
Vitamin D, which is well known to maintain calcium homeostasis, plays an important role in various cellular processes. It regulates the proliferation and differentiation of several normal cells, including immune and neoplastic cells, influences the cell cycle, and stimulates cell maturation and apoptosis through a mechanism dependent on the vitamin D receptor. The involvement of vitamin D in breast cancer development has been observed in numerous clinical studies. However, not all studies support the protective effect of vitamin D against the development of this condition. Furthermore, animal studies have revealed that calcitriol or its analogs may stimulate tumor growth or metastasis in some breast cancer models. It has been postulated that the effect of vitamin D on T helper (Th) 17 lymphocytes is one of the mechanisms promoting metastasis in these murine models. Herein we present a literature review on the existing data according to the interplay between vitamin D, Th17 cell and breast cancer. We also discuss the effects of this vitamin on Th17 lymphocytes in various disease entities known to date, due to the scarcity of scientific data on Th17 lymphocytes and breast cancer. The presented data indicate that the effect of vitamin D on breast cancer development depends on many factors, such as age, menopausal status, or obesity. According to that, more extensive clinical trials and studies are needed to assess the importance of vitamin D in breast cancer, especially when no correlations seem to be obvious.
Cancers (Basel). 2022-7-27
Recent Results Cancer Res. 2003
Endocr Relat Cancer. 2022-1-24
Clin Immunol. 2016-4-1
J Steroid Biochem Mol Biol. 2015-4
Ann N Y Acad Sci. 2014-3-26
Int J Mol Sci. 2025-7-22
Breast Cancer (Dove Med Press). 2024-4-12
Mol Biol Rep. 2024-1-25
Explor Target Antitumor Ther. 2023
Int J Mol Sci. 2021-11-25
Front Oncol. 2021-5-31
Front Immunol. 2021
Front Cell Dev Biol. 2021-2-4