Evidence map›Paper›PMID 37363722›Full record

ReviewFrontiers in cell and developmental biology2023

Evolution and function of calponin and transgelin.

Tzu-Bou Hsieh, J-P Jin

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Altered TAGLN Expression During HBV Replication Correlates with OPA1 Levels.International journal of molecular sciences · 2026
    Article
  2. The circadian clock controls hepatic stellate cell activation via a BMAL1/CK1ε/REV-ERBα/transgelin signaling pathway.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Smooth muscle contractile cytoskeleton in health and disease.Journal of muscle research and cell motility · 2026
    Review
  5. Article
  6. Article
  7. Article
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  9. Cocaine abuse and its impact on the thymus and spleen.Histology and histopathology · 2025
    Review
  10. Article
  11. Review
  12. Article
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  14. Observational
  15. Article
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

2 authors at 2 institutions in 1 country.

Tzu-Bou HsiehDepartment of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, United States.
J-P JinDepartment of Physiology and Biophysics, University of Illinois at Chicago College of Medicine, Chicago, IL, United States.
University of Illinois Chicago · USWayne State University · US

Funding

Regulation of Troponin I in Cardiac Adaptation & FailureR01HL127691 · NHLBI · WAYNE STATE UNIVERSITY · PI Jian-Ping Jin · 2016 to 2026
$3.5M
Rabbit model for cystic fibrosisR01HL133162 · NHLBI · WAYNE STATE UNIVERSITY · PI JIN, JIAN-PING, XU, JIE · 2016 to 2019
$2.9M
Targeting Troponin T Regulation to Sustain Cardiac Function in Heart FailureR01HL138007 · NHLBI · WAYNE STATE UNIVERSITY · PI Jian-Ping Jin · 2018 to 2026
$2.4M
NHLBI NIH HHS R01 HL127691NHLBI NIH HHS R01 HL133162NHLBI NIH HHS R01 HL138007
6 · The paper itself

Abstract

Calponin and transgelin (originally named SM22) are homologous cytoskeleton proteins that regulate actin-activated myosin motor functions in smooth muscle contraction and non-muscle cell motility during adhesion, migration, proliferation, phagocytosis, wound healing, and inflammatory responses. They are abundant cytoskeleton proteins present in multiple cell types whereas their physiological functions remain to be fully established. This focused review summarizes the evolution of genes encoding calponin and transgelin and their isoforms and discusses the structural similarity and divergence in vertebrate and invertebrate species in the context of functions in regulating cell motility. As the first literature review focusing on the evolution of the calponin-transgelin family of proteins in relevance to their structure-function relationship, the goal is to outline a foundation of current knowledge for continued investigations to understand the biological functions of calponin and transgelin in various cell types during physiological and pathological processes.

Indexed as

calponincell motilitycytoskeletonevolutionisoform genesstructure-function relationshiptransgelin

Identifiers

PMID37363722
PMCPMC10285543
OpenAlexW4380051982

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.