Effect of 1α,25(OH)2D3-Treated M1 and M2 Macrophages on Cell Proliferation and Migration Ability in Ovarian Cancer
The biological active form of vitamin D3, 1α,25-dehydroxyvitamin D3 [1α,25(OH) 2 D 3 ], exerts pleiotropic effects including bone mineralization, anti-tumor, as well as immunomodulator. This study aimed to explore the potential impact of 1α,25(OH) 2 D 3 on tumor-associated macrophages (TAMs) infiltr...
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Published in | Nutrition and cancer Vol. 74; no. 7; pp. 2632 - 2643 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Mahwah
Taylor & Francis
2022
Taylor & Francis Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | The biological active form of vitamin D3, 1α,25-dehydroxyvitamin D3 [1α,25(OH)
2
D
3
], exerts pleiotropic effects including bone mineralization, anti-tumor, as well as immunomodulator. This study aimed to explore the potential impact of 1α,25(OH)
2
D
3
on tumor-associated macrophages (TAMs) infiltration in ovarian cancer. Firstly, human monocytic THP-1 cells were differentiated into macrophages (M0) in the presence of phorbol 12-myristate 13-acetate (PMA). In Vivo, 1α,25(OH)
2
D
3
not only reversed the polarization of M2 macrophages, but also decreased the proliferation and migration abilities of ovarian cancer cells induced by M2 macrophages supernatant. Furthermore, 1α,25(OH)
2
D
3
dramatically decreased the secretion of TGF-β1 and MMP-9 in M2 macrophages. However, no significant effect was observed in 1α,25(OH)
2
D
3
treated M1 macrophages. In Vivo, vitamin D3 had an inhibitive effect of 1α,25(OH)
2
D
3
-treated M2 macrophages on tumorigenesis. In addition, we conducted the association of TAMs with the poor prognosis of patients with ovarian cancer by meta-analysis, which suggested the higher proportion of M2 macrophages was related to the poorer prognosis in ovarian cancer. Collectively, these results identified distinct roles of 1α,25(OH)
2
D
3
treated M1 and M2 macrophages on cell proliferation and migration abilities in ovarian cancer. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0163-5581 1532-7914 |
DOI: | 10.1080/01635581.2021.2014903 |