1,25-Dihydroxyvitamin D3 and a superagonistic analog in combination with paclitaxel or suberoylanilide hydroxamic acid have potent antiproliferative effects on anaplastic thyroid cancer

被引:32
作者
Clinckspoor, Isabelle [1 ]
Verlinden, Lieve [1 ]
Overbergh, Lutgart [1 ]
Korch, Christopher [2 ]
Bouillon, Roger [1 ]
Mathieu, Chantal [1 ]
Verstuyf, Annemieke [1 ]
Decallonne, Brigitte [1 ]
机构
[1] Catholic Univ Louvain, Lab Expt Geneeskunde & Endocrinol LEGENDO, Fac Med, B-3000 Louvain, Belgium
[2] Univ Colorado, Ctr Canc, DNA Sequencing & Anal Core, Aurora, CO 80045 USA
关键词
Thyroid; Cancer; Vitamin D; Nonsteroidal analog; SAHA; Paclitaxel; HISTONE DEACETYLASE INHIBITOR; VITAMIN-D; ANTITUMOR-ACTIVITY; BREAST-CANCER; IN-VITRO; PHASE-I; CARCINOMA; EXPRESSION; RECEPTOR; CELLS;
D O I
10.1016/j.jsbmb.2010.12.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Anaplastic thyroid cancer represents one of the most aggressive cancers. The active form of vitamin D, 1,25-dihydroxyvitamin D-3 (1,25(OH)(2)D-3), has been shown to have antiproliferative and/or redifferentiating properties in several malignancies, including thyroid cancer. The objective of this study was to investigate the effects of 1,25(OH)(2) D-3 and the superagonistic analog CD578 in anaplastic thyroid cancer, alone or in combination with paclitaxel, a taxane, and suberoylanilide hydroxamic acid (SAHA), a potent histone deacetylase inhibitor with promising effects in undifferentiated thyroid cancer. Four human thyroid cancer cell lines (FTC-133, C643, 8505C and HTh74) were treated with 1,25(OH)(2) D-3 or CD578, alone or in combination with paclitaxel or SAHA. Effects on cell growth and differentiation were evaluated. Clear effects on growth arrest were observed in a clonogenic assay, and absolute cell counts demonstrated a 24-36% reduction in all cell lines after 72 h treatment with 1,25(OH)(2)D-3 (10(-6) M) and a 60% inhibition after 120 h in the most sensitive cell line HTh74. A similar growth inhibition was shown after treatment with a 1000-fold lower concentration of analog CD578. This growth arrest was explained by antiproliferative effects, further supported by an increased % of cells in the G(0)-G(1) phase of the cell cycle and by a decreased transcription factor E2F1 mRNA expression. Combination treatments of 1,25(OH)(2)D-3 or CD578 with paclitaxel or SAHA resulted in an additive and in some conditions a synergistic effect on the inhibition of proliferation. Redifferentiation analysis revealed only a modest increase in sodium iodide symporter and thyroglobulin mRNA expression after treatment with 1,25(OH)(2)D-3, without additive effect after combination treatment. No effects were observed on TSH-receptor or thyroid peroxidase mRNA expression. Our in vitro findings demonstrate that the superagonistic vitamin D analog CD578 holds promise as adjuvant antiproliferative therapy of anaplastic thyroid cancer, especially in combination with other drugs such as paclitaxel or SAHA. (C) 2010 Elsevier Ltd. All rights reserved.
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页码:1 / 9
页数:9
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