Evidence map›Paper›PMID 40110186›Full record

ReviewFrontiers in physiology2025

Review of electrophysiological models to study membrane potential changes in breast cancer cell transformation and tumor progression.

Chitaranjan Mahapatra, Arnaw Kishore, Jineetkumar Gawad, Ahmed Al-Emam, Riad Azzam Kouzeiha, Maher Ali Rusho

Abstract readReview
In one paragraph

Review in Frontiers in physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Cancer: A bioelectric disease?Clinical and translational medicine · 2026
    Review
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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.

Chitaranjan MahapatraParis Saclay Institute of Neuroscience, Paris Saclay University, Saclay, France.
Arnaw KishoreMicrobiology and Immunology, Xavier University School of Medicine, Aruba, Netherlands.
Jineetkumar GawadDepartment of Pharmaceutical Chemistry, VIVA Institute of Pharmacy, Virar, India.
Ahmed Al-EmamDepartment of Pathology, College of Medicine, King Khalid University, Asir, Saudi Arabia.
Riad Azzam KouzeihaFaculty of Medical Sciences, Lebanese University, Hadath Campus, Beirut, Lebanon.
Maher Ali RushoDepartment of Biomedical Engineering, University of Colorado Boulder, Boulder, CO, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transformation of normal breast cells into cancerous cells is a complex process influenced by both genetic and microenvironmental factors. Recent studies highlight the significant role of membrane potential (Vm) alterations in this transformation. Cancer cells typically exhibit a depolarized resting membrane potential (RMP) compared to normal cells, which correlates with increased cellular activity and more aggressive cancer behavior. These RMP and Vm changes are associated with altered ion channel activity, altered calcium dynamics, mitochondrial dysfunction, modified gap junction communication, and disrupted signaling pathways. Such fluctuations in RMP and Vm influence key processes in cancer progression, including cell proliferation, migration, and invasion. Notably, more aggressive subtypes of breast cancer cells display more frequent and pronounced Vm fluctuations. Understanding the electrical properties of cancer cells provides new insights into their behavior and offers potential therapeutic targets, such as ion channels and Vm regulation. This review synthesizes current research on how various factors modulate membrane potential and proposes an electrophysiological model of breast cancer cells based on experimental and clinical data from the literature. These findings may pave the way for novel pharmacological targets for clinicians, researchers, and pharmacologists in treating breast cancer.

Indexed as

breast cancercalcium dynamicselectrophysiological modelgap junctionion channelsmembrane potential

Identifiers

PMID40110186
PMCPMC11920174

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.