Oncogenic potential of EAG K+ channels
Open accessAbstract
We have investigated the possible implication of the cell cycle-regulated K(+) channel ether à go-go (EAG) in cell proliferation and transformation. We show that transfection of EAG into mammalian cells confers a transformed phenotype. In addition, human EAG mRNA is detected in several somatic cancer cell lines, despite being preferentially expressed in brain among normal tissues. Inhibition of EAG expression in several of these cancer cell lines causes a significant reduction of cell proliferation. Moreover, the expression of EAG favours tumour progression when transfected cells are injected into immune-depressed mice. These data provide evidence for the oncogenic potential of EAG.
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Inhibition of EAG channel expression reduces proliferation in several cancer cell lines, whereas implantation of CHO cells over-expressing EAG channels in mice induces tumors.
“Inhibition of EAG channel expression reduces proliferation in several cancer cell lines, whereas implantation of CHO cells over-expressing EAG channels in mice induces tumors (Pardo et al., 1999).”
From Membrane potential and cancer progression (2013) · cites this paper as Pardo et al., 1999
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- Authors
- Pardo, L. A., del Camino, D., Sánchez, A., Alves, F., Brüggemann, A., Beckh, S., & Stühmer, W.
- Affiliations
- Max Planck Institute of Experimental Medicine (DE)
- Universitätsmedizin Göttingen (DE)
- Corresponding author
- Pardo, Luis A.
- Venue
- The EMBO Journal
- Published
- 1999-10-15
- Volume
- 18
- Issue
- 20
- Pages
- 5540-5547
- ISSN
- 0261-4189 (ISSN-L)
- 1460-2075
- PMC
- PMC1171622
- OpenAlex
- W1970120474
- Cited by
- 446
- References
- 0
- Citations by year
- 2026: 9 · 2025: 6 · 2024: 11 · 2023: 12 · 2022: 13 · 2021: 12 · 2020: 22 · 2019: 13 · 2018: 7 · 2017: 22 · 2016: 27 · 2015: 20 · 2014: 24 · 2013: 24 · 2012: 30
- FWCI
- 2.53
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The EMBO Journal (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Keywords
- ether-a-go-go potassium channel, oncogenicity, cell transformation, cell proliferation, tumor progression, tumor xenografts
- MeSH terms
- Animals, Base Sequence, Cell Division, Cell Transformation, Neoplastic, Cloning, Molecular, Humans, Molecular Sequence Data, Neoplasms, Experimental, Phenotype, RNA, Messenger, Tumor Cells, Cultured, Potassium Channels, Gene Expression, Mice, SCID, In Situ Hybridization, Fluorescence, DNA Primers, Oligodeoxyribonucleotides, Antisense, Mice, Ether-A-Go-Go Potassium Channels
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