Evidence map›Paper›PMID 40846899›Full record

ArticleCommunications biology2025

Maspin/SerpinB5 is a cytoskeleton-binding protein that regulates epithelial cell shape.

Luiz E da Silva, Lia M G Paim, Tatiana Lyalina, Ana P J Menezes, Julia P C da Cunha, Susanne Bechstedt, Nathalie Cella

Abstract read
In one paragraph

Article in Communications biology, 2025. 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

7 authors.

Luiz E da SilvaDepartment of Cell and Developmental Biology, University of São Paulo, São Paulo, Brazil.
Lia M G PaimDepartment of Anatomy and Cell Biology, McGill University, Montreal, Canada.
Tatiana LyalinaDepartment of Anatomy and Cell Biology, McGill University, Montreal, Canada.
Ana P J MenezesLaboratory of Cell Cycle, Instituto Butantan, São Paulo, Brazil.
Julia P C da CunhaLaboratory of Cell Cycle, Instituto Butantan, São Paulo, Brazil.
Susanne BechstedtDepartment of Anatomy and Cell Biology, McGill University, Montreal, Canada.ORCID http://orcid.org/0000-0002-4706-9975
Nathalie CellaDepartment of Cell and Developmental Biology, University of São Paulo, São Paulo, Brazil. ncella@usp.br.ORCID http://orcid.org/0000-0001-6060-1076

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Brazilian Federal Agency for the Support and Evaluation of Graduate Education) 88887.506347/2020-00Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Brazilian Federal Agency for the Support and Evaluation of Graduate Education) 88887.816589/2023-00Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Brazilian Federal Agency for the Support and Evaluation of Graduate Education) 88887.835982/2023-00Fundação de Amparo à Pesquisa do Estado de São Paulo (São Paulo Research Foundation) 18/15553-9Fundação de Amparo à Pesquisa do Estado de São Paulo (São Paulo Research Foundation) 2021/12268-4Fundação de Amparo à Pesquisa do Estado de São Paulo (São Paulo Research Foundation) 23/08391-0Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) PJT-156193Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada (Conseil de Recherches en Sciences Naturelles et en Génie du Canada) RGPIN-2017-04649
6 · The paper itself

Abstract

Maspin/SerpinB5 is an abundant and pleiotropic protein mostly expressed by epithelia. Initially described as a tumor suppressor, it has been reported as a regulator of cell adhesion, migration, and invasion. How intracellular Maspin orchestrates these processes is poorly understood. In this study, we utilized Affinity purification-Mass spectrometry (AP/MS) alongside in vitro reconstitution assays to establish that Maspin directly interacts with microtubules and microfilaments. Additionally, CRISPR/Cas9-mediated GFP tagging of endogenous Maspin, combined with immunostaining, revealed its localization at the cortical cytoskeleton and the mitotic spindle. Depletion of Maspin by RNAi and CRISPR/Cas9 in non-transformed epithelial cell lines modifies cell-cell contact and promotes cytoskeletal rearrangements. Concomitantly, we observed a modest upregulation of mesenchymal markers during interphase and abnormal cell rounding during mitosis. An evaluation of Maspin's effect on microtubules revealed that it suppresses their growth in vitro and in cells. Collectively, these results demonstrate that Maspin acts dynamically at the interface of the cytoskeleton and adhesion sites, modulating cell shape.

Indexed as

Cell ShapeCytoskeletonEpithelial CellsSerpinsAnimalsCell AdhesionHumansMicrotubulesSERPIN-B5Serpins

Identifiers

PMID40846899
PMCPMC12373898

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.