Evidence map›Paper›PMID 25829491›Full record

ArticleThe Journal of biological chemistry2015

Nuclear localization and functional characteristics of voltage-gated potassium channel Kv1.3.

Soo Hwa Jang, Jun Kyu Byun, Won-Il Jeon, Seon Young Choi, Jin Park, Bo Hyung Lee, Ji Eun Yang, Jin Bong Park, Scott M O'Grady, Dae-Yong Kim and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 52 citations in OpenAlex.

  1. Identification of Novel Kv1.3 Channel-Interacting Proteins Using Proximity Labelling in T-Cells.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2025
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Targeting Ion Channels for Cancer Treatment: Current Progress and Future Challenges.Reviews of physiology, biochemistry and pharmacology · 2022
    Review
  9. Review
  10. Article
  11. Article
  12. Discovery of KMedicinal research reviews · 2021
    Review
  13. Article
  14. Article
  15. Pharmacological modulation of mitochondrial ion channels.British journal of pharmacology · 2019
    Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Targeting Mitochondrial Ion Channels to Fight Cancer.International journal of molecular sciences · 2018
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 2 countries.

Soo Hwa JangFrom the Laboratories of Veterinary Pharmacology and the Biomedical Research Center, School of Biological Sciences, University of Ulsan, Ulsan 680-749, Korea.
Jun Kyu ByunFrom the Laboratories of Veterinary Pharmacology and.
Won-Il JeonFrom the Laboratories of Veterinary Pharmacology and.
Seon Young ChoiFrom the Laboratories of Veterinary Pharmacology and.
Jin Parkthe Department of Chemistry, Soongsil University, Seoul 156-743, Korea.
Bo Hyung LeeFrom the Laboratories of Veterinary Pharmacology and.
Ji Eun YangFrom the Laboratories of Veterinary Pharmacology and.
Jin Bong Parkthe Department of Physiology, School of Medicine, Chungnam National University, Daejeon 305-764, Korea, and.
Scott M O'Gradythe Department of Animal Science and Integrative Biology and Physiology, University of Minnesota, St. Paul, Minnesota 55455.
Dae-Yong KimVeterinary Pathology, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University, Seoul 151-742, Korea.
Pan Dong RyuFrom the Laboratories of Veterinary Pharmacology and.
Sang-Woo Joothe Department of Chemistry, Soongsil University, Seoul 156-743, Korea.
So Yeong LeeFrom the Laboratories of Veterinary Pharmacology and leeso@snu.ac.kr.
Seoul National University · KRSoongsil University · KRChungnam National University · KRUniversity of Minnesota · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is widely known that ion channels are expressed in the plasma membrane. However, a few studies have suggested that several ion channels including voltage-gated K(+) (Kv) channels also exist in intracellular organelles where they are involved in the biochemical events associated with cell signaling. In the present study, Western blot analysis using fractionated protein clearly indicates that Kv1.3 channels are expressed in the nuclei of MCF7, A549, and SNU-484 cancer cells and human brain tissues. In addition, Kv1.3 is located in the plasma membrane and the nucleus of Jurkat T cells. Nuclear membrane hyperpolarization after treatment with margatoxin (MgTX), a specific blocker of Kv1.3 channels, provides evidence for functional channels at the nuclear membrane of A549 cells. MgTX-induced hyperpolarization is abolished in the nuclei of Kv1.3 silenced cells, and the effects of MgTX are dependent on the magnitude of the K(+) gradient across the nuclear membrane. Selective Kv1.3 blockers induce the phosphorylation of cAMP response element-binding protein (CREB) and c-Fos activation. Moreover, Kv1.3 is shown to form a complex with the upstream binding factor 1 in the nucleus. Chromatin immunoprecipitation assay reveals that Sp1 transcription factor is directly bound to the promoter region of the Kv1.3 gene, and the Sp1 regulates Kv1.3 expression in the nucleus of A549 cells. These results demonstrate that Kv1.3 channels are primarily localized in the nucleus of several types of cancer cells and human brain tissues where they are capable of regulating nuclear membrane potential and activation of transcription factors, such as phosphorylated CREB and c-Fos.

Indexed as

BrainCell MembraneCell NucleusCyclic AMP Response Element-Binding ProteinGene SilencingHumansJurkat CellsKv1.3 Potassium ChannelMembrane PotentialsPhosphorylationScorpion VenomsSerum Response FactorSp1 Transcription FactorCREB1 protein, humanCyclic AMP Response Element-Binding ProteinKv1.3 Potassium ChannelmargatoxinScorpion VenomsSerum Response FactorSP1 protein, humanSp1 Transcription FactorcAMP response element-binding protein (CREB)cell fractionationc-Fosion channelKv channelsnuclear membrane potentialnucleusspecificity protein 1 (Sp1)UBF1

Identifiers

PMID25829491
PMCPMC4432276
OpenAlexW2026597643

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.