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- W1976466424 abstract "Research over the last decade has revealed that CYP11A1 can hydroxylate the side chain of vitamin D3 at carbons 17, 20, 22 and 23 to produce at least 10 metabolites, with 20(OH)D3, 20,23(OH)2D3, 20,22(OH)2D3, 17,20(OH)2D3 and 17,20,23(OH)3D3 being the main products. However, CYP11A1 does not act on 25(OH)D3. The placenta, adrenal glands and epidermal keratinocytes have been shown to metabolize vitamin D3 via this CYP11A1-mediated pathway that is modified by the activity of CYP27B1, with 20(OH)D3 (the major metabolite), 20,23(OH)2D3, 1,20(OH)2D3, 1,20,23(OH)3D3 and 17,20,23(OH)3D3 being detected, defining these secosteroids as endogenous regulators/natural products. This is supported by the detection of a mono-hydroxyvitamin D3 with the retention time of 20(OH)D3 in human serum. In new work presented here we demonstrate that the CYP11A1-initiated pathways also occurs in Caco-2 colon cells. Our previous studies show that 20(OH)D3 and 20,23(OH)2D3 are non-calcemic at pharmacological doses, dependent in part on their lack of a C1α hydroxyl group. In epidermal keratinocytes, 20(OH)D3, 20(OH)D2 and 20,23(OH)2D3 inhibited cell proliferation, stimulated differentiation and inhibited NF-κB activity with potencies comparable to 1,25(OH)2D3, acting as partial agonists on the VDR. 22(OH)D3 and 20,22(OH)2D3, as well as secosteroids with a short or no side chain, showed antiproliferative and prodifferentiation effects, however, with lower potency than 20(OH)D3 and 20,23(OH)2D3. The CYP11A1-derived secosteroids also inhibited melanocyte proliferation while having no effect on melanogenesis, and showed anti-melanoma activities in terms of inhibiting proliferation and the ability to grow in soft agar. Furthermore, 20(OH)D3 and 20,23(OH)2D3 showed anti-fibrosing effects in vitro, and also in vivo for the former. New data presented here shows that 20(OH)D3 inhibits LPS-induced production of TNFα in the J774 line, TNFα and IL-6 in peritoneal macrophages and suppresses the production of proinflammatory Th1/Th17-related cytokines, while promoting the production of the anti-inflammatory cytokine IL-10 in vivo. In summary, CYP11A1 initiates new pathways of vitamin D metabolism in a range of tissues and products could have important physiological roles at the local or systemic level. In the skin, CYP11A1-derived secosteroids could serve both as endogenous regulators of skin functions and as excellent candidates for treatment of hyperproliferative and inflammatory skin disorders, and skin cancer. This article is part of a Special Issue entitled '16th Vitamin D Workshop'." @default.
- W1976466424 created "2016-06-24" @default.
- W1976466424 creator A5000432967 @default.
- W1976466424 creator A5008065253 @default.
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- W1976466424 creator A5050860545 @default.
- W1976466424 creator A5053365826 @default.
- W1976466424 creator A5058359268 @default.
- W1976466424 date "2014-10-01" @default.
- W1976466424 modified "2023-10-16" @default.
- W1976466424 title "The role of CYP11A1 in the production of vitamin D metabolites and their role in the regulation of epidermal functions" @default.
- W1976466424 cites W139833353 @default.
- W1976466424 cites W1495372639 @default.
- W1976466424 cites W1523735757 @default.
- W1976466424 cites W1540236839 @default.
- W1976466424 cites W1543661309 @default.
- W1976466424 cites W1563558118 @default.
- W1976466424 cites W1882211948 @default.
- W1976466424 cites W1887054657 @default.
- W1976466424 cites W1965916393 @default.
- W1976466424 cites W1966414524 @default.
- W1976466424 cites W1970516100 @default.
- W1976466424 cites W1971273108 @default.
- W1976466424 cites W1971605460 @default.
- W1976466424 cites W1972743589 @default.
- W1976466424 cites W1973355249 @default.
- W1976466424 cites W1977233186 @default.
- W1976466424 cites W1982421644 @default.
- W1976466424 cites W1982557271 @default.
- W1976466424 cites W1988506918 @default.
- W1976466424 cites W1989168127 @default.
- W1976466424 cites W1995138037 @default.
- W1976466424 cites W1999178887 @default.
- W1976466424 cites W2000227232 @default.
- W1976466424 cites W2006784527 @default.
- W1976466424 cites W2008276067 @default.
- W1976466424 cites W2008297014 @default.
- W1976466424 cites W2009171847 @default.
- W1976466424 cites W2010930504 @default.
- W1976466424 cites W2011607277 @default.
- W1976466424 cites W2011645313 @default.
- W1976466424 cites W2012700441 @default.
- W1976466424 cites W2013252828 @default.
- W1976466424 cites W2013777284 @default.
- W1976466424 cites W2018517476 @default.
- W1976466424 cites W2020048876 @default.
- W1976466424 cites W2022074542 @default.
- W1976466424 cites W2024440231 @default.
- W1976466424 cites W2025627627 @default.
- W1976466424 cites W2027278752 @default.
- W1976466424 cites W2028177638 @default.
- W1976466424 cites W2028455155 @default.
- W1976466424 cites W2028875889 @default.
- W1976466424 cites W2033599074 @default.
- W1976466424 cites W2040722453 @default.
- W1976466424 cites W2042394868 @default.
- W1976466424 cites W2042794704 @default.
- W1976466424 cites W2043584813 @default.
- W1976466424 cites W2048531918 @default.
- W1976466424 cites W2052382142 @default.
- W1976466424 cites W2062933772 @default.
- W1976466424 cites W2064094052 @default.
- W1976466424 cites W2065938328 @default.
- W1976466424 cites W2066368067 @default.
- W1976466424 cites W2071882832 @default.
- W1976466424 cites W2072799292 @default.
- W1976466424 cites W2074330545 @default.
- W1976466424 cites W2076615170 @default.
- W1976466424 cites W2077590888 @default.
- W1976466424 cites W2082168591 @default.
- W1976466424 cites W2083203284 @default.
- W1976466424 cites W2083444816 @default.
- W1976466424 cites W2088149676 @default.
- W1976466424 cites W2090312069 @default.
- W1976466424 cites W2092118888 @default.
- W1976466424 cites W2102377211 @default.
- W1976466424 cites W2105892849 @default.
- W1976466424 cites W2106044877 @default.
- W1976466424 cites W2108296645 @default.
- W1976466424 cites W2114496307 @default.
- W1976466424 cites W2116100637 @default.
- W1976466424 cites W2118228269 @default.
- W1976466424 cites W2122507575 @default.
- W1976466424 cites W2125720142 @default.
- W1976466424 cites W2127898028 @default.
- W1976466424 cites W2127919481 @default.
- W1976466424 cites W2128830532 @default.
- W1976466424 cites W2139659644 @default.
- W1976466424 cites W2147452643 @default.
- W1976466424 cites W2148336091 @default.
- W1976466424 cites W2153488515 @default.
- W1976466424 cites W2154250040 @default.
- W1976466424 cites W2157471721 @default.
- W1976466424 cites W2158555665 @default.
- W1976466424 cites W2167997754 @default.
- W1976466424 cites W2169858408 @default.
- W1976466424 cites W4229927405 @default.
- W1976466424 doi "https://doi.org/10.1016/j.jsbmb.2013.10.012" @default.