Originally published as JHC exPRESS on November 28, 2005.
doi:10.1369/jhc.5A6734.2005
Journal of Histochemistry and Cytochemistry
Volume 54 (3): 355-361, 2006
Copyright ©The Histochemical Society, Inc.
25-Hydroxyvitamin D3 1
-Hydroxylase and Vitamin D Receptor Expression in Papillary Thyroid Carcinoma
K. Khadzkou,
P. Buchwald,
G. Westin,
H. Dralle,
G. Åkerström and
P. Hellman
Department of Surgical Sciences, University Hospital, Uppsala, Sweden (KK,PB,GW,GÅ,PH); Department of Surgery, Vitebsk State Medical University, Vitebsk, Belarus (KK); and Department of Surgery, Martin-Luther University, Halle-Wittenberg, Germany (HD)
Correspondence to: Per Hellman, MD, PhD, Department of Surgery, University Hospital, SE-751 85, Uppsala, Sweden. E-mail: per.hellman{at}surgsci.uu.se
Vitamin D receptor (VDR) and 25-hydroxyvitamin D3 1-
-hydroxylase expression have recently been shown to be upregulated in several tumors and thought to represent an important endogenous response to tumor progression. Little is known about the expression of these proteins in thyroid carcinoma, although previous reports have documented evidence of the biological effect of vitamin D in thyroid cells. Using paraffin-embedded and frozen sections of papillary thyroid carcinoma, we utilized real-time quantitative RT-PCR and immunohistochemistry to characterize the expression of VDR and 1-
-hydroxylase in thyroid follicular cells, with special emphasis on papillary thyroid carcinoma (PTC). VDR and 1-
-hydroxylase expression were increased in PTC compared with normal thyroid tissue and especially high in areas of lymphocyte infiltration. Expression of VDR and 1-
-hydroxylase in PTC may be compatible with an overall favorable prognosis for this tumor type and may constitute important prerequisites for using vitamin D and/or vitamin D analogs in the treatment of PTC. (J Histochem Cytochem 54:355361, 2006)
Key Words: thyroid carcinoma vitamin D 1-
-hydroxylase immunohistochemistry RT-PCR

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