Evidence map›Paper›PMID 40802255›Full record

ReviewMolecular biology of the cell2025

Please inhibit responsibly: Natural and synthetic actin toxins as useful tools in cell biology.

Katrina B Velle, Masayuki Onishi

Abstract readReview
In one paragraph

Review in Molecular biology of the cell, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Katrina B VelleDepartment of Biology, University of Massachusetts Dartmouth, North Dartmouth, MA 02747.
Masayuki OnishiDepartment of Biology, Duke University, Durham, NC 27708.

Funding

Defining cytoskeletal mechanisms driving cell motility in NaegleriaR00GM147656 · NIGMS · UNIVERSITY OF MASSACHUSETTS DARTMOUTH · PI Katrina Velle · 2024 to 2026
$747k
NIGMS NIH HHS R00 GM147656
6 · The paper itself

Abstract

The actin cytoskeleton drives many critical cell functions, including motility, division, and vesicular trafficking. To fulfill these functions, actin networks are dynamic and tightly regulated by dozens of proteins that cause actin to assemble and disassemble at the proper time and place. Given the importance of actin to a cell's biology, it is not surprising that some organisms produce toxins that target actin dynamics to incapacitate prey, win turf wars, or as a defense against predation. For decades, cell biologists have leveraged these toxins and synthesized new ones to cause defects in the structure and function of the actin cytoskeleton. Here, we provide an overview of commonly used actin inhibitors and their origins, as well as best practices for their use in biological studies.

Indexed as

Actin CytoskeletonActinsToxins, BiologicalAnimalsCell BiologyHumansActinsToxins, Biological

Identifiers

PMID40802255
PMCPMC12444908

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.