Evidence map›Paper›PMID 33829040›Full record

ArticleFrontiers in molecular biosciences2021

IGF2BP1, a Conserved Regulator of RNA Turnover in Cancer.

Markus Glaß, Danny Misiak, Nadine Bley, Simon Müller, Sven Hagemann, Bianca Busch, Alexander Rausch, Stefan Hüttelmaier

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  10. Survival-Related Genes on Chromosomes 6 and 17 in Medulloblastoma.International journal of molecular sciences · 2024
    Article
  11. IGF2BPs as novel mGenes & diseases · 2024
    Review
  12. Association of insulin-like growth factor II mrna-binding protein 3 (IMP3) expression with prognostic and morphological factors in endometrial cancer.Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia · 2024
    Article
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  14. mScientific reports · 2023
    Article
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  17. 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

8 authors at 1 institution in 1 country.

Markus GlaßInstitute of Molecular Medicine, Martin Luther University Halle-Wittenberg, Halle, Germany.
Danny MisiakInstitute of Molecular Medicine, Martin Luther University Halle-Wittenberg, Halle, Germany.
Nadine BleyInstitute of Molecular Medicine, Martin Luther University Halle-Wittenberg, Halle, Germany.
Simon MüllerInstitute of Molecular Medicine, Martin Luther University Halle-Wittenberg, Halle, Germany.
Sven HagemannInstitute of Molecular Medicine, Martin Luther University Halle-Wittenberg, Halle, Germany.
Bianca BuschInstitute of Molecular Medicine, Martin Luther University Halle-Wittenberg, Halle, Germany.
Alexander RauschInstitute of Molecular Medicine, Martin Luther University Halle-Wittenberg, Halle, Germany.
Stefan HüttelmaierInstitute of Molecular Medicine, Martin Luther University Halle-Wittenberg, Halle, Germany.
Martin Luther University Halle-Wittenberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The oncofetal IGF2 mRNA-binding protein 1 (IGF2BP1) promotes tumor progression in a variety of solid tumors and its expression is associated with adverse prognosis. The main role proposed for IGF2BP1 in cancer cells is the stabilization of mRNAs encoding pro-oncogenic factors. Several IGF2BP1-RNA association studies, however, revealed a plethora of putative IGF2BP1-RNA targets. Thus, at present the main conserved target RNAs and pathways controlled by IGF2BP1 in cancer remain elusive. In this study, we present a set of genes and cancer hallmark pathways showing a conserved pattern of deregulation in dependence of IGF2BP1 expression in cancer cell lines. By the integrative analysis of these findings with publicly available cancer transcriptome and IGF2BP1-RNA association data, we compiled a set of prime candidate target mRNAs. These analyses confirm a pivotal role of IGF2BP1 in controlling cancer cell cycle progression and reveal novel cancer hallmark pathways influenced by IGF2BP1. For three novel target mRNAs identified by these studies, namely AURKA, HDLBP and YWHAZ, we confirm IGF2BP1 mRNA stabilization. In sum our findings confirm and expand previous findings on the pivotal role of IGF2BP1 in promoting oncogenic gene expression by stabilizing target mRNAs in a mainly 3'UTR, m

Indexed as

AURKAcancerE2FHDLBPIGF2BP1YWHAZ

Identifiers

PMID33829040
PMCPMC8019740
OpenAlexW3138274008

What Socratic holds

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LicenceCC BY
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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 Socratic graph.