Evidence map›Paper›PMID 34439247›Full record

ArticleCancers2021

The RNA-Binding Protein ESRP1 Modulates the Expression of RAC1b in Colorectal Cancer Cells.

Marta Manco, Ugo Ala, Daniela Cantarella, Emanuela Tolosano, Enzo Medico, Fiorella Altruda, Sharmila Fagoonee

Abstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
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  4. ESRP1 exerts anti-tumor role by promoting ferroptosis in diffuse-type gastric cancer.Journal of experimental & clinical cancer research : CR · 2025
    Article
  5. 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

7 authors.

Marta MancoMolecular Biotechnology Center, Department of Molecular Biotechnology and Health Sciences, University of Turin, 10126 Turin, Italy.
Ugo AlaDepartment of Veterinary Science, University of Turin, Largo Paolo Braccini 2, 10095 Grugliasco, Italy.ORCID 0000-0001-5408-6397
Daniela CantarellaDepartment of Oncology, University of Torino, S.P. 142, km 3.95, Torino, 10060 Candiolo, Italy.
Emanuela TolosanoMolecular Biotechnology Center, Department of Molecular Biotechnology and Health Sciences, University of Turin, 10126 Turin, Italy.ORCID 0000-0002-1622-2340
Enzo MedicoDepartment of Oncology, University of Torino, S.P. 142, km 3.95, Torino, 10060 Candiolo, Italy.ORCID 0000-0002-3917-2438
Fiorella AltrudaDepartment of Veterinary Science, University of Turin, Largo Paolo Braccini 2, 10095 Grugliasco, Italy.ORCID 0000-0002-6238-1860
Sharmila FagooneeInstitute of Biostructure and Bioimaging, National Research Council (CNR) c/o Molecular Biotechnology Center, 10126 Turin, Italy.ORCID 0000-0001-6070-6716

Funding

University of Turin RILO
6 · The paper itself

Abstract

RNA binding proteins are well recognized as critical regulators of tumorigenic processes through their capacity to modulate RNA biogenesis, including alternative splicing, RNA stability and mRNA translation. The RNA binding protein Epithelial Splicing Regulatory Protein 1 (ESRP1) can act as a tumor suppressor or promoter in a cell type- and disease context-dependent manner. We have previously shown that elevated expression of ESRP1 in colorectal cancer cells can drive tumor progression. To gain further insights into the pro-tumorigenic mechanism of action of ESRP1, we performed cDNA microarray analysis on two colorectal cells lines modulated for ESRP1 expression. Intriguingly, RAC1b was highly expressed, both at mRNA and protein levels, in ESRP1-overexpressing cells, while the opposite trend was observed in ESRP1-silenced CRC cells. Moreover,

Indexed as

alternative splicingbioinformatics analysiscDNA microarraycolorectal cancerESRP1RAC1RAC1bRNA-binding protein

Identifiers

PMID34439247
PMCPMC8392041

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Registered trials

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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.