Evidence map›Paper›PMID 34979904›Full record

ArticleBMC molecular and cell biology2022

Compression enhances invasive phenotype and matrix degradation of breast Cancer cells via Piezo1 activation.

Mingzhi Luo, Grace Cai, Kenneth K Y Ho, Kang Wen, Zhaowen Tong, Linhong Deng, Allen P Liu

Open access · goldAbstract read
In one paragraph

Article in BMC molecular and cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

57 citing papers in PubMed, 75 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Metabolic starvation-induced cell swelling drives solid stress in tumors.bioRxiv : the preprint server for biology · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. PIEZO channels as multimodal mechanotransducers.Biochemical Society transactions · 2025
    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

7 authors at 2 institutions in 2 countries.

Mingzhi LuoInstitute of Biomedical Engineering and Health Sciences, Changzhou University, Changzhou, Jiangsu, People's Republic of China.
Grace CaiApplied Physics Program, University of Michigan, Ann Arbor, MI, USA.
Kenneth K Y HoDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA.
Kang WenInstitute of Biomedical Engineering and Health Sciences, Changzhou University, Changzhou, Jiangsu, People's Republic of China.
Zhaowen TongApplied Physics Program, University of Michigan, Ann Arbor, MI, USA.
Linhong DengInstitute of Biomedical Engineering and Health Sciences, Changzhou University, Changzhou, Jiangsu, People's Republic of China. dlh@cczu.edu.cn.
Allen P LiuDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA. allenliu@umich.edu.
University of Michigan–Ann Arbor · USChangzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUncontrolled growth in solid breast cancer generates mechanical compression that may drive the cancer cells into a more invasive phenotype, but little is known about how such compression affects the key events and corresponding regulatory mechanisms associated with invasion of breast cancer cells including cellular behaviors and matrix degradation.

resultsHere we show that compression enhanced invasion and matrix degradation of breast cancer cells. We also identified Piezo1 as the putative mechanosensitive cellular component that transmitted compression to not only enhance the invasive phenotype, but also induce calcium influx and downstream Src signaling. Furthermore, we demonstrated that Piezo1 was mainly localized in caveolae, and both Piezo1 expression and compression-enhanced invasive phenotype of the breast cancer cells were reduced when caveolar integrity was compromised by either knocking down caveolin1 expression or depleting cholesterol content.

conclusionsTaken together, our data indicate that mechanical compression activates Piezo1 channels to mediate enhanced breast cancer cell invasion, which involves both cellular events and matrix degradation. This may be a critical mechanotransduction pathway during breast cancer metastasis, and thus potentially a novel therapeutic target for the disease.

Indexed as

Breast NeoplasmsIon ChannelsMechanotransduction, CellularFemaleHumansPhenotypeSignal TransductionIon ChannelsPIEZO1 protein, humanBreast cancer cellCompressionInvasionPiezo1

Identifiers

PMID34979904
PMCPMC8722159
OpenAlexW4205850442

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.