Evidence map›Paper›PMID 37746658›Full record

ArticleResearch (Washington, D.C.)2023

The Mechanics of Tumor Cells Dictate Malignancy via Cytoskeleton-Mediated APC/Wnt/β-Catenin Signaling.

Xi Chen, Zichen Xu, Kai Tang, Guanshuo Hu, Pengyu Du, Junfang Wang, Cunyu Zhang, Ying Xin, Keming Li, Qiantang Zhang and 5 more

Abstract read
In one paragraph

Article in Research (Washington, D.C.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Review
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  7. Intercellular contractile force attenuates chemosensitivity through Notch-MVP-mediated nuclear drug export.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  15. Premetastatic niche mechanics and organotropism in breast cancer.npj biological physics and mechanics · 2025
    Review
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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

15 authors.

Xi ChenThe Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen, 518057, China.
Zichen XuKey Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing, 400030, China.
Kai TangDepartment of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong, China.
Guanshuo HuThe Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen, 518057, China.
Pengyu DuDepartment of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong, China.
Junfang WangDepartment of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong, China.
Cunyu ZhangResearch Institute of Smart Ageing, The Hong Kong Polytechnic University, Hong Kong, China.
Ying XinDepartment of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong, China.
Keming LiDepartment of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong, China.
Qiantang ZhangKey Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing, 400030, China.
Jianjun HuDepartment of Pathology, Guizhou Provincial People's Hospital, Guiyang, Guizhou, 550002, China.
Zhuxue ZhangDepartment of Pathology, Guizhou Provincial People's Hospital, Guiyang, Guizhou, 550002, China.
Mo YangDepartment of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong, China.
Guixue WangKey Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing, 400030, China.
Youhua TanThe Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen, 518057, China.ORCID https://orcid.org/0000-0003-1411-1265

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor cells progressively remodel cytoskeletal structures and reduce cellular stiffness during tumor progression, implicating the correlation between cell mechanics and malignancy. However, the roles of tumor cell cytoskeleton and the mechanics in tumor progression remain incompletely understood. We report that softening/stiffening tumor cells by targeting actomyosin promotes/suppresses self-renewal in vitro and tumorigenic potential in vivo. Weakening/strengthening actin cytoskeleton impairs/reinforces the interaction between adenomatous polyposis coli (APC) and β-catenin, which facilitates β-catenin nuclear/cytoplasmic localization. Nuclear β-catenin binds to the promoter of Oct4, which enhances its transcription that is crucial in sustaining self-renewal and malignancy. These results demonstrate that the mechanics of tumor cells dictate self-renewal through cytoskeleton-APC-Wnt/β-catenin-Oct4 signaling, which are correlated with tumor differentiation and patient survival. This study unveils an uncovered regulatory role of cell mechanics in self-renewal and malignancy, and identifies tumor cell mechanics as a hallmark not only for cancer diagnosis but also for mechanotargeting.

Identifiers

PMID37746658
PMCPMC10513157

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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.