Evidence map›Paper›PMID 26686085›Full record

ArticleOncogene2016

Tumor-suppressor NFκB2 p100 interacts with ERK2 and stabilizes PTEN mRNA via inhibition of miR-494.

Y Wang, J Xu, G Gao, J Li, H Huang, H Jin, J Zhu, X Che, C Huang

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  15. Article
  16. Article
  17. Regulation of PTEN expression by noncoding RNAs.Journal of experimental & clinical cancer research : CR · 2018
    Review
  18. Noncanonical NF-κB in Cancer.Biomedicines · 2018
    Review
  19. Review
  20. 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

9 authors at 1 institution in 1 country.

Y WangNelson Institute of Environmental Medicine, New York University School of Medicine, Tuxedo, NY, USA.
J XuNelson Institute of Environmental Medicine, New York University School of Medicine, Tuxedo, NY, USA.
G GaoNelson Institute of Environmental Medicine, New York University School of Medicine, Tuxedo, NY, USA.
J LiNelson Institute of Environmental Medicine, New York University School of Medicine, Tuxedo, NY, USA.
H HuangNelson Institute of Environmental Medicine, New York University School of Medicine, Tuxedo, NY, USA.
H JinNelson Institute of Environmental Medicine, New York University School of Medicine, Tuxedo, NY, USA.
J ZhuNelson Institute of Environmental Medicine, New York University School of Medicine, Tuxedo, NY, USA.
X CheNelson Institute of Environmental Medicine, New York University School of Medicine, Tuxedo, NY, USA.
C HuangNelson Institute of Environmental Medicine, New York University School of Medicine, Tuxedo, NY, USA.
New York University · US

Funding

RESEARCH IN ENVIRONMENTAL HEALTH SCIENCES (CENTER GRANT)P30ES000260 · NIEHS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ZELIKOFF, JUDITH TERRY · 1985 to 2020
$26.1M
Reagent/Service CoreP01CA165980 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI TANG, ERIC MOON-SHONG M. · 2013 to 2023
$13.5M
Molecular Mechanisms of Nickel-Induced TumorigenicityR01CA112557 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI HUANG, CHUANSHU · 2004 to 2016
$2.9M
Mechanisms underlying therapeutic effect of a new compound Isorhapontigenin (ISO)R01CA177665 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI HUANG, CHUANSHU · 2013 to 2018
$1.7M
NCI NIH HHS P01 CA165980NCI NIH HHS R01 CA112557NCI NIH HHS R01 CA177665NIEHS NIH HHS P30 ES000260
6 · The paper itself

Abstract

Emerging evidence from The Cancer Genome Atlas has revealed that nuclear factor κB2 (nfκb2) gene encoding p100 is genetically deleted or mutated in human cancers, implicating NFκB2 as a potential tumor suppressor. However, the molecular mechanism underlying the antitumorigenic action of p100 remains poorly understood. Here we report that p100 inhibits cancer cell anchorage-independent growth, a hallmark of cellular malignancy, by stabilizing the tumor-suppressor phosphatase and tensin homolog (PTEN) mRNA via a mechanism that is independent of p100's inhibitory role in NFκB activation. We further demonstrate that the regulatory effect of p100 on PTEN expression is mediated by its downregulation of miR-494 as a result of the inactivation of extracellular signal-regulated kinase 2 (ERK2), in turn leading to inhibition of c-Jun/activator protein-1-dependent transcriptional activity. Furthermore, we identify that p100 specifically interacts with non-phosphorylated ERK2 and prevents ERK2 phosphorylation and nuclear translocation. Moreover, the death domain at C-terminal of p100 is identified as being crucial and sufficient for its interaction with ERK2. Taken together, our findings provide novel mechanistic insights into the understanding of the tumor-suppressive role for NFκB2 p100.

Indexed as

RNA StabilityActive Transport, Cell NucleusHCT116 CellsHumansMicroRNAsMitogen-Activated Protein Kinase 1NF-kappa B p52 SubunitPhosphorylationProto-Oncogene Proteins c-junPTEN PhosphohydrolaseSignal TransductionTumor Suppressor ProteinsMAPK1 protein, humanMicroRNAsMIRN494 microRNA, humanMitogen-Activated Protein Kinase 1NF-kappa B p52 SubunitNFKB2 protein, humanProto-Oncogene Proteins c-junPTEN PhosphohydrolaseTumor Suppressor Proteins

Identifiers

PMID26686085
PMCPMC4916044
OpenAlexW2235193128

What OpenQuestion holds

Textmetadata
LicenceTDM
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.