Evidence map›Paper›PMID 25670080›Full record

ArticleCancer cell2015

A targetable GATA2-IGF2 axis confers aggressiveness in lethal prostate cancer.

Samuel J Vidal, Veronica Rodriguez-Bravo, S Aidan Quinn, Ruth Rodriguez-Barrueco, Amaia Lujambio, Estrelania Williams, Xiaochen Sun, Janis de la Iglesia-Vicente, Albert Lee, Ben Readhead and 11 more

Abstract read
In one paragraph

Article in Cancer cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
13.4field-weighted citation impact, top 1% 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

92 citing papers in PubMed, 154 citations in OpenAlex.

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  16. Role of the pioneer transcription factor GATA2 in health and disease.Journal of molecular medicine (Berlin, Germany) · 2023
    Review
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32 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 4 institutions in 1 country.

Samuel J VidalCollege of Physicians and Surgeons, Columbia University, New York, NY 10032, USA; Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Veronica Rodriguez-BravoMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
S Aidan QuinnDepartment of Pathology and Cell Biology, Columbia University, New York, NY, USA 10032, USA.
Ruth Rodriguez-BarruecoDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Amaia LujambioCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Estrelania WilliamsDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Xiaochen SunTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Janis de la Iglesia-VicenteDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Albert LeeDepartment of Biomedical Informatics, Center for Computational Biology and Bioinformatics, Columbia University, New York, NY 10031, USA.
Ben ReadheadDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Xintong ChenTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Matthew GalskyTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Berta EsteveDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Daniel P PetrylakYale Comprehensive Cancer Center, Yale School of Medicine, New Haven, CT 06510, USA.
Joel T DudleyDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Raul RabadanDepartment of Biomedical Informatics, Center for Computational Biology and Bioinformatics, Columbia University, New York, NY 10031, USA.
Jose M SilvaDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Yujin HoshidaTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Scott W LoweCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Carlos Cordon-CardoDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. Electronic address: carlos.cordon-cardo@mssm.edu.
Josep Domingo-DomenechDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. Electronic address: josep.domingo-domenech@mssm.edu.
Icahn School of Medicine at Mount Sinai · USColumbia University · USMemorial Sloan Kettering Cancer Center · USYale Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Scientific ReagentsP01CA087497 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI PETRINI, JOHN HJ · 2000 to 2021
$35.4M
COMPUTATIONAL AND FUNCTIONAL APPROACHES TO VALIDATING CANCER GENOME TARGETSU01CA168409 · NCI · COLD SPRING HARBOR LABORATORY · PI POWERS, SCOTT · 2012 to 2016
$7.3M
Molecular Prognostic Indicators in Liver Cirrhosis and CancerR01DK099558 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HOSHIDA, YUJIN · 2013 to 2016
$2.6M
Training Program in Computational BiologyT32GM082797 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HONIG, BARRY H · 2008 to 2015
$1.4M
Howard Hughes Medical InstituteNCI NIH HHS P01 CA087497NCI NIH HHS P30 CA008748NCI NIH HHS U01 CA168409NIDDK NIH HHS R01 DK099558NIGMS NIH HHS T32 GM082797
6 · The paper itself

Abstract

Elucidating the determinants of aggressiveness in lethal prostate cancer may stimulate therapeutic strategies that improve clinical outcomes. We used experimental models and clinical databases to identify GATA2 as a regulator of chemotherapy resistance and tumorigenicity in this context. Mechanistically, direct upregulation of the growth hormone IGF2 emerged as a mediator of the aggressive properties regulated by GATA2. IGF2 in turn activated IGF1R and INSR as well as a downstream polykinase program. The characterization of this axis prompted a combination strategy whereby dual IGF1R/INSR inhibition restored the efficacy of chemotherapy and improved survival in preclinical models. These studies reveal a GATA2-IGF2 aggressiveness axis in lethal prostate cancer and identify a therapeutic opportunity in this challenging disease.

Indexed as

AnimalsAntigens, CDCell ProliferationDrug Resistance, NeoplasmGATA2 Transcription FactorHumansInsulin-Like Growth Factor IIMaleMiceProstatic Neoplasms, Castration-ResistantReceptor, InsulinSignal TransductionXenograft Model Antitumor AssaysAntigens, CDGATA2 protein, humanGATA2 Transcription FactorIGF2 protein, humanINSR protein, humanInsulin-Like Growth Factor IIReceptor, Insulin

Identifiers

PMID25670080
PMCPMC4356948
OpenAlexW2012730900

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.