Evidence map›Paper›PMID 29861849›Full record

ArticleOncotarget2018

Real-time scratch assay reveals mechanisms of early calcium signaling in breast cancer cells in response to wounding.

Stephen J P Pratt, Erick O Hernández-Ochoa, Rachel M Lee, Eleanor C Ory, James S Lyons, Humberto C Joca, Ashley Johnson, Keyata Thompson, Patrick Bailey, Cornell J Lee and 7 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
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  4. Nematic cell alignment directs calcium waves.bioRxiv : the preprint server for biology · 2025
    Article
  5. Review
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  13. Mechanoactivation of NOX2-generated ROS elicits persistent TRPM8 CaProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
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

17 authors at 2 institutions in 1 country.

Stephen J P PrattDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD, USA.
Erick O Hernández-OchoaDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD, USA.
Rachel M LeeDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Eleanor C OryDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
James S LyonsDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD, USA.
Humberto C JocaDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD, USA.
Ashley JohnsonDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Keyata ThompsonDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Patrick BaileyDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD, USA.
Cornell J LeeDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Trevor MathiasDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Michele I VitoloDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Matt TrudeauDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Joseph P StainsDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD, USA.
Christopher W WardDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD, USA.
Martin F SchneiderDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD, USA.
Stuart S MartinDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD, USA.
University of Maryland, Baltimore · USUNC Lineberger Comprehensive Cancer Center

Funding

Training Grant in Cancer BiologyT32CA154274 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI Toni M Antalis, CURT I CIVIN · 2011 to 2026
$6.8M
Tubulin microtentacles in detached mammary epithelial cellsR01CA124704 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI MARTIN, STUART S · 2007 to 2025
$5.7M
TRAINING PROGRAM IN INTEGRATIVE MEMBRANE BIOLOGYT32GM008181 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI RIZZO, MEGAN A, TRUDEAU, MATTHEW C · 1987 to 2022
$4.9M
Targeting microtubule stabilization to reduce breast tumor metastasisR01CA154624 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI MARTIN, STUART S · 2012 to 2023
$3.4M
Medical Scientist Training ProgramT32GM092237 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI ROGHMANN, MARY-CLAIRE · 2010 to 2019
$3.0M
Microtubule Regulated Mechanotransduction in Skeletal MuscleR01AR071618 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI WARD, CHRISTOPHER WILLIAM · 2017 to 2021
$2.6M
Osteocyte CaMKII as a Critical Regulator of Bone Physiology and AnabolismR01AR071614 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Joseph P. Stains · 2018 to 2026
$2.6M
PTEN loss increases efficiency of breast tumor metastasisK01CA166576 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI VITOLO, MICHELE I · 2013 to 2017
$524k
NCI NIH HHS K01 CA166576NCI NIH HHS R01 CA124704NCI NIH HHS R01 CA154624NCI NIH HHS T32 CA154274NIAMS NIH HHS R01 AR071614NIAMS NIH HHS R01 AR071618NIGMS NIH HHS T32 GM008181NIGMS NIH HHS T32 GM092237
6 · The paper itself

Abstract

Aggressive cellular phenotypes such as uncontrolled proliferation and increased migration capacity engender cellular transformation, malignancy and metastasis. While genetic mutations are undisputed drivers of cancer initiation and progression, it is increasingly accepted that external factors are also playing a major role. Two recently studied modulators of breast cancer are changes in the cellular mechanical microenvironment and alterations in calcium homeostasis. While many studies investigate these factors separately in breast cancer cells, very few do so in combination. This current work sets a foundation to explore mechano-calcium relationships driving malignant progression in breast cancer. Utilizing real-time imaging of an

Indexed as

calciumhuman breast cancerintercellular signalingmechanotransductionpurinergic receptor

Identifiers

PMID29861849
PMCPMC5982755
OpenAlexW2803395247

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.