Evidence map›Paper›PMID 28279977›Full record

ArticleThe EMBO journal2017

AKT-phosphorylated FOXO1 suppresses ERK activation and chemoresistance by disrupting IQGAP1-MAPK interaction.

Chun-Wu Pan, Xin Jin, Yu Zhao, Yunqian Pan, Jing Yang, R Jeffrey Karnes, Jun Zhang, Liguo Wang, Haojie Huang

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
6.6field-weighted citation impact, top 2% 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

74 citing papers in PubMed, 123 citations in OpenAlex.

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14 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Chun-Wu PanDepartment of Urology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID 0000-0002-2941-8991
Xin JinDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
Yu ZhaoDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
Yunqian PanDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
Jing YangDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
R Jeffrey KarnesDepartment of Urology, Mayo Clinic, Rochester, MN, USA.
Jun ZhangDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Liguo WangDivision of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, USA.
Haojie HuangDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA huang.haojie@mayo.edu.ORCID 0000-0003-2751-6413
Mayo Clinic in Arizona · USMayo Clinic in Florida · USShanghai Jiao Tong University · CN

Funding

Role of proinflammatory cytokine-induced AR degradation in castration-resistant prostate cancerR01CA130908 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI HUANG, HAOJIE · 2010 to 2021
$3.5M
Role of FOXO1 Inactivation in Prostate TumorigenesisR01CA134514 · NCI · UNIVERSITY OF MINNESOTA · PI HUANG, HAOJIE · 2009 to 2019
$3.3M
Role of RUNX2 in prostate cancer intratumoral androgen synthesis and progressionR01CA193239 · NCI · MAYO CLINIC ROCHESTER · PI HUANG, HAOJIE · 2015 to 2019
$1.8M
NCI NIH HHS R01 CA130908NCI NIH HHS R01 CA134514NCI NIH HHS R01 CA193239
6 · The paper itself

Abstract

Nuclear FOXO proteins act as tumor suppressors by transcriptionally activating genes involved in apoptosis and cell cycle arrest, and these anticancer functions are inhibited by AKT-induced phosphorylation and cytoplasmic sequestration of FOXOs. We found that, after AKT-mediated phosphorylation at serine 319, FOXO1 binds to IQGAP1, a hub for activation of the MAPK pathway, and impedes IQGAP1-dependent phosphorylation of ERK1/2 (pERK1/2). Conversely, decreased FOXO1 expression increases pERK1/2 in cancer cell lines and correlates with increased pERK1/2 levels in patient specimens and disease progression. Treatment of cancer cells with PI3K inhibitors or taxane causes FOXO1 localization in the nucleus, increased expression of pERK1/2, and drug resistance. These effects are reversed by administering a small FOXO1-derived phospho-mimicking peptide inhibitor

Indexed as

Drug Resistance, NeoplasmMAP Kinase Signaling SystemAnimalsBridged-Ring CompoundsCell Line, TumorForkhead Box Protein O1HumansMaleMiceMice, Inbred NODMice, SCIDMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Phosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsPhosphorylationBridged-Ring CompoundsForkhead Box Protein O1FOXO1 protein, humanIQ motif containing GTPase activating protein 1MAPK1 protein, humanMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Phosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsProto-Oncogene Proteins c-aktras GTPase-Activating ProteinstaxaneTaxoidsAKTcancerchemoresistanceFOXO1MAPK

Identifiers

PMID28279977
PMCPMC5391142
OpenAlexW2592240998

What OpenQuestion holds

Textmetadata
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.