Evidence map›Paper›PMID 42272789›Full record

ArticleBiophysical reviews2026

The unconventional regulation of non-muscle myosins.

Andrew T Lombardo

Abstract read
In one paragraph

Article in Biophysical reviews, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Andrew T LombardoJacobs School of Medicine and Biomedical Sciences, Department of Biochemistry, University at Buffalo, Buffalo, NY, USA.ORCID 0000-0002-1814-5748

Funding

The Cytoskeletal Drivers of Cell PolarityR35GM156870 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Andrew Thomas Lombardo · 2025 to 2026
$757k
NIGMS NIH HHS R35 GM156870
6 · The paper itself

Abstract

Myosins are actin-based molecular motors that power diverse forms of cellular motility across life. Initially characterized as the contractile machinery of muscle, the superfamily now includes numerous non-muscle classes with distinct cellular functions. Over the past decades, work across numerous actin-based systems has uncovered multiple modes of non-muscle myosin control. Recent advances now expand and, in some cases, challenge conventional regulatory paradigms, underscoring the complexity and adaptability of myosin function in cellular contexts. In this short review, I begin with a concise summary of the major canonical regulatory systems for non-muscle myosins. I follow this by highlighting the major novel regulatory findings from the last decade specifically relating to protein-binding partner activation, structural lipid-binding motifs, co-assembly of mixed classes of myosins, and the regulation of multi-motor complexes by the nanoscale organization of cellular actin. This review will appeal to the general scientific reader aiming to understand the mechanisms regulating myosins outside of the context of muscle and the current state of the non-muscle myosin field.

Indexed as

ActinCell polarityCytoskeletonMechanobiologyMolecular motorsMyosins

Identifiers

PMID42272789
PMCPMC13249394

What OpenQuestion holds

Textmetadata
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.