Ether à go-go Potassium Channels as Human Cervical Cancer Markers

Ether à go-go (EAG) potassium channels display oncogenic properties. In normal tissues, EAG mRNA is almost exclusively expressed in brain, but it is expressed in several somatic cancer cell lines, including HeLa, from cervix. Antisense experiments against eag reduce cell proliferation in some cancer cell lines, and inhibition of EAG-mediated currents has been suggested to decrease cell proliferation in a melanoma cell line. Because of the potential clinical relevance of EAG, we investigated EAG mRNA expression in the following fresh samples from human uterine cervix: 5 primary cultures obtained from cancerous biopsies, 1 cancerous fresh tissue, and 12 biopsies of control normal tissue. All of the control cervical samples came from patients with negative pap smears. Reverse transcription-PCR and Southern-blot experiments revealed eag expression in 100% of the cancerous samples and in 33% of the normal biopsies. Immunochemistry experiments showed the presence of EAG channel protein in cells from the primary cultures and in cervical cancer biopsies sections from the same patients. In addition, we looked for EAG-mediated currents in the cultures from cervical cancer cells. Here we show for the first time EAG channel activity in human tumors. Patch-clamp recordings showed typical EAG-mediated currents modulated by magnesium and displaying a pronounced Cole-Moore shift. Because EAG expression and channel activity have been suggested to be important in cell proliferation, our findings strongly support the idea of considering EAG as a tumor marker as well as a potential membrane therapeutic target for cervical cancer.

[1]  B. Sakmann,et al.  Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches , 1981, Pflügers Archiv.

[2]  S. Bellone,et al.  Selection of HER-2/neu-positive tumor cells in early stage cervical cancer: implications for Herceptin-mediated therapy. , 2003, Gynecologic oncology.

[3]  E. Wanke,et al.  Cell Cycle-dependent Expression of HERG1 and HERG1B Isoforms in Tumor Cells* , 2003, The Journal of Biological Chemistry.

[4]  M. Brizzi,et al.  HERG potassium channels are constitutively expressed in primary human acute myeloid leukemias and regulate cell proliferation of normal and leukemic hemopoietic progenitors , 2002, Leukemia.

[5]  S. Heinemann,et al.  Effects of Imipramine on Ion Channels and Proliferation of IGR1 Melanoma Cells , 2002, The Journal of Membrane Biology.

[6]  E. Newell,et al.  Functional Up-regulation of HERG K+ Channels in Neoplastic Hematopoietic Cells* , 2002, The Journal of Biological Chemistry.

[7]  R. Toillon,et al.  Changes in the K+ current-density of MCF-7 cells during progression through the cell cycle: possible involvement of a h-ether.a-gogo K+ channel. , 2001, Receptors & channels.

[8]  L. Pardo,et al.  Cytoskeletal interactions determine the electrophysiological properties of human EAG potassium channels , 2000, Pflügers Archiv.

[9]  E. Wanke,et al.  HERG potassium channels are more frequently expressed in human endometrial cancer as compared to non-cancerous endometrium , 2000, British Journal of Cancer.

[10]  L. Pardo,et al.  Oncogenic potential of EAG K+ channels , 1999, The EMBO journal.

[11]  S. Heinemann,et al.  Identification of Ether à Go-Go and Calcium-Activated Potassium Channels in Human Melanoma Cells , 1999, The Journal of Membrane Biology.

[12]  L. Pardo,et al.  Cell Cycle–related Changes in the Conducting Properties of r-eag K+ Channels , 1998, The Journal of cell biology.

[13]  C. Bader,et al.  An ether ‐à‐go‐go K+ current, Ih‐eag, contributes to the hyperpolarization of human fusion‐competent myoblasts , 1998, The Journal of physiology.

[14]  C. Bader,et al.  Cloning of a human ether‐a‐go‐go potassium channel expressed in myoblasts at the onset of fusion , 1998, FEBS letters.

[15]  S. Heinemann,et al.  Characterization of an eag‐like potassium channel in human neuroblastoma cells , 1998, The Journal of physiology.

[16]  L. Bianchi,et al.  herg encodes a K+ current highly conserved in tumors of different histogenesis: a selective advantage for cancer cells? , 1998, Cancer research.

[17]  L. Pardo,et al.  Mitosis-promoting factor-mediated suppression of a cloned delayed rectifier potassium channel expressed in Xenopus oocytes. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[18]  J. Ruppersberg Ion Channels in Excitable Membranes , 1996 .