Evidence map›Paper›PMID 29755635›Full record

ArticleBiomicrofluidics2018

Microfluidic platform for probing cancer cells migration property under periodic mechanical confinement.

Dongce Ma, Ran Wang, Shuxun Chen, Tao Luo, Yu-Ting Chow, Dong Sun

Open access · bronzeAbstract read
In one paragraph

Article in Biomicrofluidics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. The Cancer Microenvironment: Mechanical Challenges of the Metastatic Cascade.Frontiers in bioengineering and biotechnology · 2021
    Review
  8. Article
  9. 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 1 institution in 1 country.

Dongce MaDepartment of Mechanical and Biomedical Engineering, City University of Hong Kong, Kowloon Tong, Hong Kong.
Ran WangDepartment of Mechanical and Biomedical Engineering, City University of Hong Kong, Kowloon Tong, Hong Kong.
Shuxun ChenDepartment of Mechanical and Biomedical Engineering, City University of Hong Kong, Kowloon Tong, Hong Kong.ORCID 0000-0003-1113-2693
Tao LuoDepartment of Mechanical and Biomedical Engineering, City University of Hong Kong, Kowloon Tong, Hong Kong.
Yu-Ting ChowDepartment of Mechanical and Biomedical Engineering, City University of Hong Kong, Kowloon Tong, Hong Kong.ORCID 0000-0001-9851-6459
Dong SunDepartment of Mechanical and Biomedical Engineering, City University of Hong Kong, Kowloon Tong, Hong Kong.ORCID 0000-0003-3945-4037
City University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer cell migration and invasion, which are involved in tumour metastasis, are hard to predict and control. Numerous studies have demonstrated that physical cues influence cancer cell migration and affect tumour metastasis. In this study, we proposed the use of a microchannel chip equipped with a number of vertical constrictions to produce periodic compression forces on cells passing through narrow channels. The chip with repeated vertical confinement was applied on adherent MHCC-97L liver cancer cells and suspended OCI-AML leukaemia cells to determine the migration ability of these cancer cells. Given the stimulation of the periodic mechanical confinement on-chip, the migration ability of cancer cells was promoted. Moreover, the migration speed increased as the stimulation was enhanced. Both AFM nanoindentation and optical stretching tests on cancer cells were performed to measure their mechanical property. After confinement stimulation, the cancer cells possessed higher deformability and lower stiffness than non-stimulating cells. The confinement stimulation altered the cell cytoskeleton, which governs the migration speed. This phenomenon was determined through gene expression analysis. The proposed on-chip cell migration assays will help characterise the migration property of cancer cells and benefit the development of new therapeutic strategies for metastasis.

Identifiers

PMID29755635
PMCPMC5924377
OpenAlexW2802584056

What OpenQuestion holds

Textmetadata
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.