Voltage-Dependent Potassium Channels Kv1.3 and Kv1.5 in Human Cancer

被引:83
作者
Bielanska, J.
Hernandez-Losa, J. [2 ]
Perez-Verdaguer, M.
Moline, T. [2 ]
Somoza, R. [2 ]
Ramon y Cajal, S. [2 ]
Condom, E. [3 ]
Ferreres, J. C. [2 ]
Felipe, A. [1 ]
机构
[1] Univ Barcelona, Fac Biol, Dept Bioquim & Biol Mol, Inst Biomed,Mol Physiol Lab, E-08028 Barcelona, Spain
[2] Hosp Univ Vall Hebron, Dept Anat Patol, Barcelona, Spain
[3] Hosp Univ Bellvitge, IDIBELL, Dept Patol & Terapeut Expt, Barcelona, Spain
关键词
Potassium channels; cancer; Kv1.3; Kv1.5; human tumors; TUMOR-CELL PROLIFERATION; K+ CHANNEL; ION CHANNELS; DELAYED RECTIFIER; MALIGNANT PROGRESSION; SKELETAL-MUSCLE; GENE PROMOTER; EXPRESSION; MACROPHAGES; ETHER;
D O I
10.2174/156800909790192400
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Membrane ion channels participate in cancerous processes such as proliferation, migration and invasion, which contribute to metastasis. Increasing evidence indicates that voltage-dependent K+ (Kv) channels are involved in the proliferation of many types of cells, including tumor cells. Kv channels have generated immense interest as a promising tool for developing new anti-tumor therapies. Therefore, the identification of potential biomarkers and therapeutic targets in specific cancers is an important prerequisite for the treatment. Since Kv1.3 and Kv1.5 are involved in the proliferation of many mammalian cells, we aimed to study the expression of Kv1.3 and Kv1.5 in a plethora of human cancers. Thus, tissues from breast, stomach, kidney, bladder, lung, skin, colon, ovary, pancreas, brain, lymph node, skeletal muscle and some of their malignant counterparts have been analyzed. Whereas Kv1.3 expression was either decreased or did not change in most tumors, Kv1.5 was overexpressed. However, the presence of Kv1.3 was mostly associated with inflammatory lymphoplasmocytic cells. Independent of the suitability of individual channels as therapeutic targets, the identification of a Kv phenotype from tumor specimens could have a diagnostic value of its own. Our results demonstrate that Kv1.5, and to some extent Kv1.3, are aberrantly expressed in a number of human cancers. These channels could serve both as novel markers of the metastatic phenotype and as potential new therapeutic targets. The concept of Kv channels as therapeutic targets or prognostic biomarkers attracts increasing interest and warrants further investigation.
引用
收藏
页码:904 / 914
页数:11
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