Evidence map›Paper›PMID 31069318›Full record

ArticleAPL bioengineering2018

The effect of mechanosensitive channel MscL expression in cancer cells on 3D confined migration.

Johanna Heureaux-Torres, Kathryn E Luker, Henry Haley, Matthew Pirone, Lap Man Lee, Yoani Herrera, Gary D Luker, Allen P Liu

Open access · goldAbstract read
In one paragraph

Article in APL bioengineering, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Johanna Heureaux-TorresDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.
Kathryn E LukerDepartment of Radiology, Center for Molecular Imaging, University of Michigan, Ann Arbor, Michigan 48109, USA.
Henry HaleyDepartment of Radiology, Center for Molecular Imaging, University of Michigan, Ann Arbor, Michigan 48109, USA.
Matthew PironeDepartment of Radiology, Center for Molecular Imaging, University of Michigan, Ann Arbor, Michigan 48109, USA.
Lap Man LeeDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.ORCID 0000-0003-2506-4329
Yoani HerreraDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.
Gary D Luker
University of Michigan · US

Funding

Repurposing mechanosensitive channels to disrupt the osmotic engine during 3D migrationR21CA198404 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, ALLEN PO-CHIH · 2015 to 2016
$349k
NCI NIH HHS R21 CA198404
6 · The paper itself

Abstract

Metastatic cancer cells migrate through constricted spaces and experience significant compressive stress, but mechanisms enabling migration in confined geometries remain unclear. Cancer cell migration within confined 3-dimensional (3D) microfluidic channels has been shown to be distinct from 2D cell migration. However, whether 3D confined migration can be manipulated by mechanosensory components has not been examined in detail. In this work, we exogenously introduced a mechanosensitive channel of large conductance (MscL) into metastatic breast cancer cells MDA-MB-231. We discovered that inducing expression of a gain-of-function G22S mutant of MscL in MDA-MB-231 cells significantly reduced spontaneous lung metastasis without affecting the growth of orthotopic tumor implants. To further investigate the effects of G22S MscL on cell migration, we designed a microfluidic device with channels of various cross-sections ranging from a 2D planar environment to narrow 3D constrictions. Both MscL G22S and control breast cancer cells migrated progressively slower in more constricted environments. Migration of cells expressing MscL G22S did not differ from control cells, even though MscL was activated in cells in constricted channels of 3

Identifiers

PMID31069318
PMCPMC6324216
OpenAlexW2806390280

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.