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Article

CYP24A1 Expression Inversely Correlates with Melanoma Progression: Clinic-Pathological Studies

1
Department of Tumor Pathology and Pathomorphology, the Ludwik Rydygier Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Torun, 85-796 Bygoszcz, Poland
2
Department of Tumor Pathology and Pathomorphology, Oncology Centre-Prof. Franciszek Łukaszczyk Memorial Hospital, 85-796 Bygoszcz, Poland
3
Departments of Pathology and Laboratory Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, USA
4
School of Chemistry and Biochemistry, the University of Western Australia, Crawley, WA 6009, Australia
5
Division of Rheumatology, Department of Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, USA
*
Authors to whom correspondence should be addressed.
Int. J. Mol. Sci. 2014, 15(10), 19000-19017; https://doi.org/10.3390/ijms151019000
Received: 16 September 2014 / Revised: 8 October 2014 / Accepted: 9 October 2014 / Published: 20 October 2014
(This article belongs to the Section Biochemistry)
The major role of 24-hydroxylase (CYP24A1) is to maintain 1,25-dihydroxyvitamin D3 (1,25(OH)2D3) homeostasis. Recently, it has been discovered that CYP24A1 also catalyses the hydroxylation of 20(OH)D3, producing dihydroxy-derivatives that show very effective antitumorigenic activities. Previously we showed a negative correlation of vitamin D receptor (VDR) and CYP27B1 expression with progression, aggressiveness and overall or disease-free survivals of skin melanomas. Therefore, we analyzed CYP24A1 expression in relation to clinicopathomorphological features of nevi, skin melanomas and metastases. In melanocytic tumors, the level of CYP24A1 was higher than in the normal epidermis. The statistically highest mean CYP24A1 level was found in nevi and early stage melanomas. With melanoma progression, CYP24A1 levels decreased and in advanced stages were comparable to the normal epidermis and metastases. Furthermore, the CYP24A1 expression positively correlated with VDR and CYP27B1, and negatively correlated with mitotic activity. Lower CYP24A1 levels correlated with the presence of ulceration, necrosis, nodular type and amelanotic phenotypes. Moreover, a lack of detectable CYP24A1 expression was related to shorter overall and disease-free survival. In conclusion, the local vitamin D endocrine system affects melanoma behavior and an elevated level of CYP24A1 appears to have an important impact on the formation of melanocytic nevi and melanomagenesis, or progression, at early stages of tumor development. View Full-Text
Keywords: skin melanoma; vitamin D; CYP24A1 skin melanoma; vitamin D; CYP24A1
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MDPI and ACS Style

Brożyna, A.A.; Jochymski, C.; Janjetovic, Z.; Jóźwicki, W.; Tuckey, R.C.; Slominski, A.T. CYP24A1 Expression Inversely Correlates with Melanoma Progression: Clinic-Pathological Studies. Int. J. Mol. Sci. 2014, 15, 19000-19017. https://doi.org/10.3390/ijms151019000

AMA Style

Brożyna AA, Jochymski C, Janjetovic Z, Jóźwicki W, Tuckey RC, Slominski AT. CYP24A1 Expression Inversely Correlates with Melanoma Progression: Clinic-Pathological Studies. International Journal of Molecular Sciences. 2014; 15(10):19000-19017. https://doi.org/10.3390/ijms151019000

Chicago/Turabian Style

Brożyna, Anna A., Cezary Jochymski, Zorica Janjetovic, Wojciech Jóźwicki, Robert C. Tuckey, and Andrzej T. Slominski 2014. "CYP24A1 Expression Inversely Correlates with Melanoma Progression: Clinic-Pathological Studies" International Journal of Molecular Sciences 15, no. 10: 19000-19017. https://doi.org/10.3390/ijms151019000

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