Functional expression of voltage-gated calcium channels in human melanoma

被引:46
作者
Das, A. [1 ]
Pushparaj, C. [1 ]
Bahi, N. [1 ]
Sorolla, A. [1 ]
Herreros, J. [1 ]
Pamplona, R. [2 ]
Vilella, R. [3 ]
Matias-Guiu, X. [4 ]
Marti, R. M. [5 ]
Canti, C. [1 ]
机构
[1] Univ Lleida IRBLleida, Lab Invest, Lerida, Spain
[2] Univ Lleida IRBLleida, Dept Expt Med, Lerida, Spain
[3] Hosp Clin Barcelona, Serv Immunol, Barcelona, Spain
[4] Univ Lleida IRBLleida, Dept Pathol & Mol Genet, Hosp Univ Arnau de Vilanova, Lerida, Spain
[5] Univ Lleida IRBLleida, Dept Dermatol, Hosp Univ Arnau de Vilanova, Lerida, Spain
关键词
melanoma; voltage-gated calcium channels; PCR; calcium imaging; viability; cell cycle; pharmacology; siRNA; CA2+ CHANNELS; NEUROENDOCRINE DIFFERENTIATION; MESSENGER-RNA; CANCER; SUBUNITS; CELLS; OVEREXPRESSION; MIBEFRADIL; BLOCKADE; CURRENTS;
D O I
10.1111/j.1755-148X.2012.00978.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The expression of voltage-gated calcium channels (VGCCs) has not been reported previously in melanoma cells in spite of increasing evidence of a role of VGCCs in tumorigenesis and tumour progression. To address this issue we have performed an extensive RT-PCR analysis of VGCC expression in human melanocytes and a range of melanoma cell lines and biopsies. In addition, we have tested the functional expression of these channels using Ca2+ imaging techniques and examined their relevance for the viability and proliferation of the melanoma cells. Our results show that control melanocytes and melanoma cells express channel isoforms belonging to the Cav1 and Cav2 gene families. Importantly, the expression of low voltage-activated Cav3 (T-type) channels is restricted to melanoma. We have confirmed the function of T-type channels as mediators of constitutive Ca2+ influx in melanoma cells. Finally, pharmacological and gene silencing approaches demonstrate a role for T-type channels in melanoma viability and proliferation. These results encourage the analysis of T-type VGCCs as targets for therapeutic intervention in melanoma tumorigenesis and/or tumour progression.
引用
收藏
页码:200 / 212
页数:14
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