The Candidate Oncogene CYP24A1: A Potential Biomarker for Colorectal Tumorigenesis

被引:109
作者
Horvath, Henrik C. [2 ]
Lakatos, Peter [2 ]
Kosa, Janos P. [2 ]
Bacsi, Krisztian
Borka, Katalin
Bises, Giovanna [1 ]
Nittke, Thomas [1 ]
Hershberger, Pamela A. [3 ]
Speer, Gabor [2 ]
Kallay, Enikoe [1 ]
机构
[1] Med Univ Vienna, Dept Pathophysiol, A-1090 Vienna, Austria
[2] Semmelweis Univ, Dept Med 1, H-1085 Budapest, Hungary
[3] Univ Pittsburgh, Inst Canc, Pittsburgh, PA USA
关键词
colorectal cancer; CYP24A1; vitamin D receptor; vitamin D; proliferation; Ki-67; adenoma; polyp; adenocarcinoma; VITAMIN-D SYSTEM; COMPARATIVE GENOMIC HYBRIDIZATION; PROSTATE-CANCER CELLS; HUMAN COLON; 25-HYDROXYVITAMIN D-3-1-ALPHA-HYDROXYLASE; D HYDROXYLASES; MESSENGER-RNA; BREAST-CANCER; D METABOLISM; IN-VIVO;
D O I
10.1369/jhc.2009.954339
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The main autocrine/paracrine role of the active metabolite of vitamin D-3, 1 alpha,25-dihydroxyvitamin D-3 (1,25-D-3), is inhibition of cell growth and induction of cell differentiation and/or apoptosis. Synthesis and degradation of the secosteroid occurs not only in the kidney but also in normal tissue or malignant extrarenal tissues such as the colon. Because 25-hydroxyvitamin D-3 24-hydroxylase (CYP24A1) is considered to be the main enzyme determining the biological half-life of 1,25-D-3, we have examined expression of the CYP24A1 mRNA (by real-time RT-PCR) and protein (by immunohistochemistry) in normal human colon mucosa, colorectal adenomas, and adenocarcinomas in 111 patients. Although 76% of the normal and benign colonic tissue was either completely devoid of or expressed very low levels of CYP24A1, in the majority of the adenocarcinomas (69%), the enzyme was present at high concentrations. A parallel increased expression of the proliferation marker Ki-67 in the same samples suggests that overexpression of CYP24A1 reduced local 1,25-D-3 availability, decreasing its antiproliferative effect. (J Histochem Cytochem 58:277-285, 2010)
引用
收藏
页码:277 / 285
页数:9
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