Evidence map›Paper›PMID 33805866›Full record

ArticleBiology2021

Cell Cytoskeleton and Stiffness Are Mechanical Indicators of Organotropism in Breast Cancer.

Kai Tang, Ying Xin, Keming Li, Xi Chen, Youhua Tan

Open access · goldAbstract read
In one paragraph

Article in Biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  9. Premetastatic niche mechanics and organotropism in breast cancer.npj biological physics and mechanics · 2025
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  11. Article
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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

5 authors at 1 institution in 2 countries.

Kai TangShenzhen Research Institute, The Hong Kong Polytechnic University, Shenzhen 518000, China.
Ying XinShenzhen Research Institute, The Hong Kong Polytechnic University, Shenzhen 518000, China.
Keming LiShenzhen Research Institute, The Hong Kong Polytechnic University, Shenzhen 518000, China.
Xi ChenShenzhen Research Institute, The Hong Kong Polytechnic University, Shenzhen 518000, China.
Youhua TanShenzhen Research Institute, The Hong Kong Polytechnic University, Shenzhen 518000, China.ORCID 0000-0003-1411-1265
Hong Kong Polytechnic University · HK

Funding

Hong Kong Polytechnic University 1-BBB1; 1-ZVPDNational Natural Science Foundation of China 11672255; 11972316Research Grants Council, University Grants Committee PolyU 252094/17EScience, Technology and Innovation Commission of Shenzhen Municipality JCYJ20170413154735522; JCYJ20200109142001798
6 · The paper itself

Abstract

Tumor metastasis involves the dissemination of tumor cells from the primary lesion to other organs and the subsequent formation of secondary tumors, which leads to the majority of cancer-related deaths. Clinical findings show that cancer cell dissemination is not random but exhibits organ preference or organotropism. While intrinsic biochemical factors of cancer cells have been extensively studied in organotropism, much less is known about the role of cell cytoskeleton and mechanics. Herein, we demonstrate that cell cytoskeleton and mechanics are correlated with organotropism. The result of cell stiffness measurements shows that breast cancer cells with bone tropism are much stiffer with enhanced F-actin, while tumor cells with brain tropism are softer with lower F-actin than their parental cells. The difference in cellular stiffness matches the difference in the rigidity of their metastasized organs. Further, disrupting the cytoskeleton of breast cancer cells with bone tropism not only elevates the expressions of brain metastasis-related genes but also increases cell spreading and proliferation on soft substrates mimicking the stiffness of brain tissue. Stabilizing the cytoskeleton of cancer cells with brain tropism upregulates bone metastasis-related genes while reduces the mechanoadaptation ability on soft substrates. Taken together, these findings demonstrate that cell cytoskeleton and biophysical properties of breast cancer subpopulations correlate with their metastatic preference in terms of gene expression pattern and mechanoadaptation ability, implying the potential role of cell cytoskeleton in organotropism.

Indexed as

cell mechanicscell stiffnesscytoskeletonmechanoadaptationorganotropism

Identifiers

PMID33805866
PMCPMC8064360
OpenAlexW3137174059

What OpenQuestion holds

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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.