Evidence map›Paper›PMID 25422049›Full record

ArticleOncology reports2015

BKCa channel inhibitor modulates the tumorigenic ability of hormone-independent breast cancer cells via the Wnt pathway.

Brandon M Schickling, Sarah K England, Nukhet Aykin-Burns, Lyse A Norian, Kimberly K Leslie, Victoria P Frieden-Korovkina

Open access · hybridAbstract read
In one paragraph

Article in Oncology reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 45% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. The journal of venomous animals and toxins including tropical diseases · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. From Channels to Canonical Wnt Signaling: A Pathological Perspective.International journal of molecular sciences · 2021
    Review
  8. Article
  9. Membrane Transporters and Channels in Melanoma.Reviews of physiology, biochemistry and pharmacology · 2021
    Review
  10. Review
  11. Voltage-Gated KFrontiers in pharmacology · 2020
    Review
  12. Article
  13. Review
  14. 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

6 authors at 3 institutions in 1 country.

Brandon M SchicklingDepartment of Obstetrics and Gynecology, University of Iowa, Iowa City, IA, USA.
Sarah K EnglandDivision of Basic Science Research, Washington University, St. Louis, MO, USA.
Nukhet Aykin-BurnsDivision of Radiation Health, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Lyse A NorianDepartment of Urology, University of Iowa, Iowa City, IA, USA.
Kimberly K LeslieDepartment of Obstetrics and Gynecology, University of Iowa, Iowa City, IA, USA.
Victoria P Frieden-KorovkinaDepartment of Obstetrics and Gynecology, University of Iowa, Iowa City, IA, USA.
University of Iowa · USUniversity of Arkansas for Medical Sciences · USWashington University in St. Louis · US

Funding

Targeted Therapy for Endometrial CancerR01CA099908 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI LESLIE, KIMBERLY K. · 2002 to 2023
$5.8M
The Use of 2-Deoxyglucose in Head and Neck Cancer TherapyR01CA133114 · NCI · UNIVERSITY OF IOWA · PI SPITZ, DOUGLAS ROBERT · 2009 to 2013
$1.5M
Sirt3: A Key Player Against PCB-Induced Mitochondrial InjuryR15ES022781 · NIEHS · UNIV OF ARKANSAS FOR MED SCIS · PI AYKIN-BURNS, NUKHET · 2013 to 2013
$443k
NCI NIH HHS R01 CA099908NCI NIH HHS R01 CA133114NCI NIH HHS R01-CA133114NCI NIH HHS R01CA99908NIEHS NIH HHS R15 ES022781
6 · The paper itself

Abstract

In breast cancers, the large conductance Ca2+ and voltage sensitive K+ (BKCa) channels have been hypothesized to function as oncoproteins, yet it remains unclear how inhibition of channel activity impacts oncogenesis. We demonstrated herein that iberiotoxin (IbTX), an inhibitor of BKCa channels, differentially modulated the in vitro tumorigenic activities of hormone-independent breast cancer cells. Specifically, in HER-2/neu-overexpressing UACC893 cells and triple‑negative MDA-MB-231 cells, IbTX selectively attenuated anchorage-independent growth with concomitant downregulation of β-catenin as well as total and phosphorylated Akt and HER-2/neu. By contrast, HER-2/neu-overexpressing SK-BR-3 cells were insensitive to IbTX. Molecular analyses showed an absence of β-catenin and a dose-dependent upregulation of total and phosphorylated Akt and HER-2/neu in these cells. Taken together, these studies identify β-catenin as a putative modulator of the inhibitory actions of IbTX in sensitive breast cancer cells.

Indexed as

Wnt Signaling PathwayAntineoplastic Agentsbeta CateninBreast NeoplasmsCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansLarge-Conductance Calcium-Activated Potassium Channel alpha SubunitsPeptidesAntineoplastic Agentsbeta CateniniberiotoxinKCNMA1 protein, humanLarge-Conductance Calcium-Activated Potassium Channel alpha SubunitsPeptides

Identifiers

PMID25422049
PMCPMC4306270
OpenAlexW2103870474

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.