Evidence map›Paper›PMID 26861754›Full record

ArticleScientific reports2016

Induction of WNT11 by hypoxia and hypoxia-inducible factor-1α regulates cell proliferation, migration and invasion.

Hiroyuki Mori, Yao Yao, Brian S Learman, Kazuhiko Kurozumi, Joji Ishida, Sadeesh K Ramakrishnan, Katherine A Overmyer, Xiang Xue, William P Cawthorn, Michael A Reid and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

43 citing papers in PubMed, 55 citations in OpenAlex.

  1. Trial
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  18. Impairment of the Hif-1α regulatory pathway in Foxn1-deficient (Foxn1FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
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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

14 authors at 4 institutions in 4 countries.

Hiroyuki MoriDepartment of Molecular &Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Yao YaoDepartment of Molecular &Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Brian S LearmanDepartment of Molecular &Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Kazuhiko KurozumiDepartment of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Joji IshidaDepartment of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Sadeesh K RamakrishnanDepartment of Molecular &Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Katherine A OvermyerDepartment of Molecular &Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Xiang XueDepartment of Molecular &Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
William P CawthornDepartment of Molecular &Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Michael A ReidDepartment of Molecular &Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Matthew TaylorDepartment of Molecular &Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Xiaomin NingDepartment of Molecular &Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Yatrik M ShahDepartment of Molecular &Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Ormond A MacDougaldDepartment of Molecular &Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
University of Michigan–Ann Arbor · USOkayama University · JPAgriculture and Forestry University · NPThe Queen's Medical Research Institute · GB

Funding

Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Joyce Lee · 2010 to 2026
$20.3M
Control of iron absorption by intestinal HIF2 in iron and hematological disordersR01DK095201 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHAH, YATRIK M · 2012 to 2025
$5.7M
The role of HIF2alpha in colon carcinogenesisR01CA148828 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHAH, YATRIK M · 2010 to 2025
$5.2M
Roles for Wnt Signaling in Adipose TissueR01DK062876 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MACDOUGALD, ORMOND A · 2003 to 2018
$5.1M
Roles for Wnt signaling in adipose tissueR56DK062876 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MACDOUGALD, ORMOND A · 2008 to 2008
$225k
NCI NIH HHS CA148828NCI NIH HHS R01 CA148828NIDDK NIH HHS DK089503NIDDK NIH HHS DK095201NIDDK NIH HHS N02 DK062876NIDDK NIH HHS P30 DK089503NIDDK NIH HHS R01 DK062876NIDDK NIH HHS R01 DK095201
6 · The paper itself

Abstract

Changes in cellular oxygen tension play important roles in physiological processes including development and pathological processes such as tumor promotion. The cellular adaptations to sustained hypoxia are mediated by hypoxia-inducible factors (HIFs) to regulate downstream target gene expression. With hypoxia, the stabilized HIF-α and aryl hydrocarbon receptor nuclear translocator (ARNT, also known as HIF-β) heterodimer bind to hypoxia response elements (HREs) and regulate expression of target genes. Here, we report that WNT11 is induced by hypoxia in many cell types, and that transcription of WNT11 is regulated primarily by HIF-1α. We observed induced WNT11 expression in the hypoxic area of allograft tumors. In addition, in mice bearing orthotopic malignant gliomas, inhibition with bevacizumab of vascular endothelial growth factor, which is an important stimulus for angiogenesis, increased nuclear HIF-1α and HIF-2α, and expression of WNT11. Gain- and loss-of-function approaches revealed that WNT11 stimulates proliferation, migration and invasion of cancer-derived cells, and increases activity of matrix metalloproteinase (MMP)-2 and 9. Since tumor hypoxia has been proposed to increase tumor aggressiveness, these data suggest WNT11 as a possible target for cancer therapies, especially for tumors treated with antiangiogenic therapy.

Indexed as

Angiogenesis InhibitorsAnimalsAryl Hydrocarbon Receptor Nuclear TranslocatorBevacizumabCell HypoxiaCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticGliomaHeLa CellsHumansHypoxia-Inducible Factor 1, alpha SubunitMiceMice, Inbred C57BLMice, KnockoutAngiogenesis InhibitorsArnt protein, mouseAryl Hydrocarbon Receptor Nuclear TranslocatorBevacizumabHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitOxygenVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouseVHL protein, mouseVon Hippel-Lindau Tumor Suppressor ProteinWnt11 protein, mouseWnt Proteins

Identifiers

PMID26861754
PMCPMC4748282
OpenAlexW2415079692

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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.