Evidence map›Paper›PMID 26416451›Full record

ArticleOncotarget2015

p62/IMP2 stimulates cell migration and reduces cell adhesion in breast cancer.

Yang Li, Giulio Francia, Jian-Ying Zhang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

28 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. IMPlications of IMP2 in RNA Biology and Disease.International journal of molecular sciences · 2025
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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

3 authors at 1 institution in 1 country.

Yang LiDepartment of Biological Sciences & NIH-Sponsored Border Biomedical Research Center, The University of Texas at El Paso, El Paso, TX 79968, USA.
Giulio FranciaDepartment of Biological Sciences & NIH-Sponsored Border Biomedical Research Center, The University of Texas at El Paso, El Paso, TX 79968, USA.
Jian-Ying ZhangDepartment of Biological Sciences & NIH-Sponsored Border Biomedical Research Center, The University of Texas at El Paso, El Paso, TX 79968, USA.
The University of Texas at El Paso · US

Funding

Autoantibodies to tumor-associated antigens as diagnostic biomarkers in liver canSC1CA166016 · NCI · UNIVERSITY OF TEXAS EL PASO · PI ZHANG, JIANYING · 2011 to 2014
$1.0M
NCI NIH HHS SC1 CA166016PHS HHS 5G12M007590
6 · The paper itself

Abstract

p62/IMP2 is an oncofetal protein that is overexpressed in several types of cancer, and is a member of the family of insulin-like growth factor 2 mRNA binding proteins. We previously reported that high levels of p62/IMP2 autoantibody are present in sera from cancer patients, compared to healthy individuals. Here, we report the overexpression of p62/IMP2 in tumor tissues of 72 out of 104 cases of human breast cancer, and high levels of p62/IMP2 autoantibody in patients' sera (in 63 out of 216 cases). To explore the role of p62/IMP2 in breast cancer progression, we generated p62/IMP2 transfected variants of two human breast cancer cell lines: MDA-MB-231 and LM2-4. Using in vitro assays we found that overexpression of p62/IMP2 can increase cell migration, and reduce cell adhesion to extracellular matrix (ECM) proteins. A Human Extracellular Matrix and Adhesion Molecules qPCR array was performed with our generated variants, and it identified a group of mRNAs whose expression was altered with p62/IMP2 overexpression, including connective tissue growth factor (CTGF) mRNA - which we show to be a p62/IMP2 binding partner. Overall, our results provide new insights into the molecular mechanism by which p62/IMP2 can contribute to breast cancer progression.

Indexed as

Cell AdhesionCell MovementAutoantibodiesBreast NeoplasmsCell Line, TumorConnective Tissue Growth FactorFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansPolymerase Chain ReactionProtein BindingProto-Oncogene Proteins c-mycRNA-Binding ProteinsRNA, MessengerRNA StabilityAutoantibodiesCCN2 protein, humanConnective Tissue Growth FactorIGF2BP2 protein, humanMYC protein, humanProto-Oncogene Proteins c-mycRNA-Binding ProteinsRNA, Messengerbreast cancercell adhesioncell migrationextracellular matrixIGF2 mRNA binding protein 2

Identifiers

PMID26416451
PMCPMC4741720
OpenAlexW2184461945

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.