Metabolic alteration of urinary steroids in pre- and post-menopausal women, and men with papillary thyroid carcinoma

Authors
Choi, Man HoMoon, Ju-YeonCho, Sung-HeeChung, Bong ChulLee, Eun Jig
Issue Date
2011-08-08
Publisher
BIOMED CENTRAL LTD
Citation
BMC CANCER, v.11
Abstract
Background: To evaluate the metabolic changes in urinary steroids in pre- and post-menopausal women and men with papillary thyroid carcinoma (PTC). Methods: Quantitative steroid profiling combined with gas chromatography-mass spectrometry was used to measure the urinary concentrations of 84 steroids in both pre- (n = 21, age: 36.95 +/- 7.19 yr) and post-menopausal female (n = 19, age: 52.79 +/- 7.66 yr), and male (n = 16, age: 41.88 +/- 8.48 yr) patients with PTC. After comparing the quantitative data of the patients with their corresponding controls (pre-menopause women: n = 24, age: 33.21 +/- 10.48 yr, post-menopause women: n = 16, age: 49.67 +/- 8.94 yr, male: n = 20, age: 42.75 +/- 4.22 yr), the levels of steroids in the patients were normalized to the mean concentration of the controls to exclude gender and menopausal variations. Results: Many urinary steroids were up-regulated in all PTC patients compared to the controls. Among them, the levels of three active androgens, androstenedione, androstenediol and 16 alpha-hydroxy DHEA, were significantly higher in the pre-menopausal women and men with PTC. The corticoid levels were increased slightly in the PTC men, while progestins were not altered in the post-menopausal PTC women. Estrogens were up-regulated in all PTC patients but 2-hydroxyestrone and 2-hydroxy-17 beta-estradiol were remarkably changed in both pre-menopausal women and men with PTC. For both menopausal and gender differences, the 2-hydroxylation, 4-hydroxylation, 2-methoxylation, and 4-methoxylation of estrogens and 16 alpha-hydroxylation of DHEA were differentiated between pre- and post-menopausal PTC women (P < 0.001). In particular, the metabolic ratio of 2-hydroxyestrone to 2-hydroxy-17 beta-estradiol, which could reveal the enzyme activity of 17 beta-hydroxysteroid dehydrogenase, showed gender differences in PTC patients (P < 1 x 10(-7)). Conclusions: These results are expected be helpful for better understanding the pathogenic differences in PTC according to gender and menopausal conditions.
Keywords
ESTROGEN-RECEPTOR; MOLECULAR MECHANISMS; ANDROGEN RECEPTORS; POOLED ANALYSIS; BREAST-CANCER; DNA-DAMAGE; CELLS; GROWTH; TUMORS; RISK; ESTROGEN-RECEPTOR; MOLECULAR MECHANISMS; ANDROGEN RECEPTORS; POOLED ANALYSIS; BREAST-CANCER; DNA-DAMAGE; CELLS; GROWTH; TUMORS; RISK; Steroids; Thyroid cancer; Menopause; Gender difference; GC-MS
ISSN
1471-2407
URI
https://pubs.kist.re.kr/handle/201004/130079
DOI
10.1186/1471-2407-11-342
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KIST Article > 2011
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