Evidence map›Paper›PMID 40141058›Full record

ReviewInternational journal of molecular sciences2025

IMPlications of IMP2 in RNA Biology and Disease.

Jessica Das, Ottavia Busia-Bourdain, Khizr M Khan, Andrew L Wolfe

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Co-expression network analysis reveals repression ofbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
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

4 authors.

Jessica DasDepartment of Biological Sciences, Hunter College, City University of New York, New York, NY 10065, USA.ORCID 0009-0008-8021-4821
Ottavia Busia-BourdainDepartment of Biological Sciences, Hunter College, City University of New York, New York, NY 10065, USA.ORCID 0009-0001-4743-5162
Khizr M KhanDepartment of Biological Sciences, Hunter College, City University of New York, New York, NY 10065, USA.ORCID 0009-0009-2221-8207
Andrew L WolfeDepartment of Biological Sciences, Hunter College, City University of New York, New York, NY 10065, USA.ORCID 0000-0003-0418-716X

Funding

Research Center in Minority Institutions (RCMI) at City CollegeU54MD017979 · NIMHD · CITY COLLEGE OF NEW YORK · PI M. Felice Marina GHILARDI · 2024 to 2026
$15.9M
TUFCCC/HC Regional Comprehensive Cancer Health PartnershipU54CA221704 · NCI · HUNTER COLLEGE · PI Ming-Chin Yeh · 2018 to 2026
$10.6M
Cellular mechanisms and therapeutic possibilities of inhibiting oncogenic KRASR00CA226363 · NCI · HUNTER COLLEGE · PI WOLFE, ANDREW L · 2021 to 2023
$747k
Cellular mechanisms and therapeutic possibilities of inhibiting oncogenic KRASK99CA226363 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WOLFE, ANDREW L · 2018 to 2020
$399k
NCI NIH HHS 5R00CA226363NCI NIH HHS K99 CA226363NCI NIH HHS R00 CA226363NCI NIH HHS U54 CA221704NIMHD NIH HHS U54 MD017979
6 · The paper itself

Abstract

Insulin-like growth factor 2 mRNA-binding protein 2 (IMP2) is an RNA-binding protein that positively regulates m6A-modified RNAs involved in critical cellular processes such as metabolism, oncogenesis, and immune function. Here, we elucidate facets of IMP2 biology, including several mechanisms of action on RNA, factors that regulate IMP2 expression, its relevant biological target RNAs, its role in normal development and disease, and its potential as a therapeutic target. IMP2 is a multi-level regulator of metabolism, influencing pathways linked to diabetes, obesity, and adipose function. Through genomic amplification and transcriptional overexpression in cancer cells, IMP2 can drive the initiation and progression of multiple cancer types, and high expression is associated with decreased overall survival of patients with cancer. IMP2 influences normal immune function, inflammation, macrophage polarization, and tumor immune evasion. IMP2 has emerged as a promising therapeutic target, particularly for cancers and metabolic diseases.

Indexed as

NeoplasmsRNARNA-Binding ProteinsAnimalsHumansIGF2BP2 protein, humanRNARNA-Binding ProteinscancerIGF2BP2immuno-oncologyIMP2m6AmetabolismmodificationRNARNA-binding proteintranslation

Identifiers

PMID40141058
PMCPMC11942581

What OpenQuestion holds

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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.