Evidence map›Paper›PMID 30374465›Full record

ArticleCommunications biology2018

Modified cantilever arrays improve sensitivity and reproducibility of nanomechanical sensing in living cells.

Samadhan B Patil, Rajai M Al-Jehani, Hashem Etayash, Valerian Turbe, Keren Jiang, Joe Bailey, Walid Al-Akkad, Rania Soudy, Kamaljit Kaur, Rachel A McKendry and 2 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-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

7 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. 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

12 authors at 4 institutions in 4 countries.

Samadhan B PatilLondon Centre for Nanotechnology, 17-19 Gordon Street, WC1H 0AH and Division of Medicine, 5 University Street, WC1E 6JF, University College London, London, UK.
Rajai M Al-JehaniUCL Institute for Liver and Digestive Health, Royal Free Hospital and NHS Foundation Trust, London, NW3 2QG, UK.
Hashem EtayashDepartment of Chemical and Materials Engineering, University of Alberta, Edmonton, AB, T6G 2V4, Canada.
Valerian TurbeLondon Centre for Nanotechnology, 17-19 Gordon Street, WC1H 0AH and Division of Medicine, 5 University Street, WC1E 6JF, University College London, London, UK.
Keren JiangDepartment of Chemical and Materials Engineering, University of Alberta, Edmonton, AB, T6G 2V4, Canada.ORCID http://orcid.org/0000-0001-6389-9875
Joe BaileyLondon Centre for Nanotechnology, 17-19 Gordon Street, WC1H 0AH and Division of Medicine, 5 University Street, WC1E 6JF, University College London, London, UK.ORCID http://orcid.org/0000-0002-1067-6560
Walid Al-AkkadUCL Institute for Liver and Digestive Health, Royal Free Hospital and NHS Foundation Trust, London, NW3 2QG, UK.
Rania SoudyDepartment of Medicine, Neuroscience and Mental Health Institute, University of Alberta, 530 Heritage Medical Research Centre, Edmonton, AB, T6G 2S2, Canada.
Kamaljit KaurChapman University School of Pharmacy (CUSP), Harry and Diane Rinker Health Science Campus, Chapman University, Irvine, CA, 92618-1908, USA.
Rachel A McKendryLondon Centre for Nanotechnology, 17-19 Gordon Street, WC1H 0AH and Division of Medicine, 5 University Street, WC1E 6JF, University College London, London, UK.
Thomas ThundatDepartment of Chemical and Materials Engineering, University of Alberta, Edmonton, AB, T6G 2V4, Canada.
Joseph W NdieyiraLondon Centre for Nanotechnology, 17-19 Gordon Street, WC1H 0AH and Division of Medicine, 5 University Street, WC1E 6JF, University College London, London, UK. j.ndieyira@ucl.ac.uk.
London Centre for Nanotechnology · GBUniversity of Alberta · CARoyal Free London NHS Foundation Trust · GBChapman University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanical signaling involved in molecular interactions lies at the heart of materials science and biological systems, but the mechanisms involved are poorly understood. Here we use nanomechanical sensors and intact human cells to provide unique insights into the signaling pathways of connectivity networks, which deliver the ability to probe cells to produce biologically relevant, quantifiable and reproducible signals. We quantify the mechanical signals from malignant cancer cells, with 10 cells per ml in 1000-fold excess of non-neoplastic human epithelial cells. Moreover, we demonstrate that a direct link between cells and molecules creates a continuous connectivity which acts like a percolating network to propagate mechanical forces over both short and long length-scales. The findings provide mechanistic insights into how cancer cells interact with one another and with their microenvironments, enabling them to invade the surrounding tissues. Further, with this system it is possible to understand how cancer clusters are able to co-ordinate their migration through narrow blood capillaries.

Identifiers

PMID30374465
PMCPMC6200835
OpenAlexW2897791953

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.