Evidence mapPaperPMID 41377763Full record

ReviewMedComm2025

Mechanical Signaling: Molecular Mechanisms, Biological Functions, Diseases, and Therapeutic Targets.

Yicen Long, Peng Wang, Jiacheng Lei, Baihai Su, Qiang Wei, Xiaojing Liu

Abstract readReview
In one paragraph

Review in MedComm, 2025. 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
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

7 citing papers in PubMed.

  1. Review
  2. 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

6 authors.

Yicen LongCollege of Polymer Science and Engineering National Key Laboratory of Advanced Polymer Materials Sichuan University Chengdu China.
Peng WangSauvage Laboratory for Smart Materials School of Materials Science and Engineering Harbin Institute of Technology (Shenzhen) Shenzhen China.
Jiacheng LeiCollege of Polymer Science and Engineering National Key Laboratory of Advanced Polymer Materials Sichuan University Chengdu China.
Baihai SuDepartment of Nephrology Kidney Research Institute West China Hospital Sichuan University Chengdu China.ORCID https://orcid.org/0000-0002-2187-8168
Qiang WeiCollege of Polymer Science and Engineering National Key Laboratory of Advanced Polymer Materials Sichuan University Chengdu China.ORCID https://orcid.org/0000-0001-5194-8262
Xiaojing LiuCollege of Polymer Science and Engineering National Key Laboratory of Advanced Polymer Materials Sichuan University Chengdu China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell mechanics is a fundamental regulator of numerous cellular processes, orchestrating critical biological activities spanning from embryogenesis to senescence. Cells continuously sense and respond to mechanical cues through specialized interactions between membrane-bound adhesion proteins, such as integrins, and adhesive ligands within the extracellular matrix (ECM). This bidirectional interaction forms the basis of mechanotransduction-a complex, dynamic process that ultimately leads to alterations in nuclear mechanics and governs essential cellular functions, including migration, tissue morphogenesis, and so on. In this review, we provide an overview of these dynamic cell-ECM interactions and delve into the intricate molecular mechanisms underlying mechanotransduction. We further introduce advanced research methodologies and emerging clinical tools used to investigate cellular mechanical phenotype, mechanotransduction, and diseases progression. In addition, we analyzed the roles of mechanical biomarkers in the development and progression of cancer, fibrosis, and aging. We highlighted the necessity of drug development targeting mechanotransduction, providing examples of drugs that have already entered clinical trials and preclinical tools. By integrating current findings and outlining emerging perspectives, this review aims to provide critical insights and inspire future efforts in understanding, manipulating, and clinically exploiting mechanotransduction-targeted markers to regulate the progression of diseases such as cancer, fibrosis, and aging.

Indexed as

agingcancerfibrosismechanobiologymechanotransduction

Identifiers

PMID41377763
PMCPMC12686584

What Socratic 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 Socratic graph.