Evidence map›Paper›PMID 30456384›Full record

ArticleLife science alliance2018

MBNL1 alternative splicing isoforms play opposing roles in cancer.

Tommaso Tabaglio, Diana Hp Low, Winnie Koon Lay Teo, Pierre Alexis Goy, Piotr Cywoniuk, Heike Wollmann, Jessica Ho, Damien Tan, Joey Aw, Andrea Pavesi and 3 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

41 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
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  7. A rare cytogenetically crypticFrontiers in oncology · 2026
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  10. Article
  11. Review
  12. Journal of Cancer · 2025
    Review
  13. Article
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  17. Article
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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

13 authors at 2 institutions in 3 countries.

Tommaso TabaglioInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore.ORCID https://orcid.org/0000-0001-6873-3073
Diana Hp LowInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore.
Winnie Koon Lay TeoInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore.
Pierre Alexis GoyInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore.
Piotr CywoniukDepartment of Gene Expression, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland.
Heike WollmannInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore.
Jessica HoInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore.ORCID https://orcid.org/0000-0003-2234-2602
Damien TanInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore.
Joey AwInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore.
Andrea PavesiInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore.
Krzysztof SobczakDepartment of Gene Expression, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland.
Dave Keng Boon WeeInstitute of High Performance Computing, Agency for Science, Technology and Research, Singapore.
Ernesto GuccioneInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore.ORCID https://orcid.org/0000-0001-7764-5307
Agency for Science, Technology and Research · SGAdam Mickiewicz University in Poznań · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The extent of and the oncogenic role played by alternative splicing (AS) in cancer are well documented. Nonetheless, only few studies have attempted to dissect individual gene function at an isoform level. Here, we focus on the AS of splicing factors during prostate cancer progression, as these factors are known to undergo extensive AS and have the potential to affect hundreds of downstream genes. We identified exon 7 (ex7) in the

Identifiers

PMID30456384
PMCPMC6238595
OpenAlexW2892297195

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.