Evidence map›Paper›PMID 27863244›Full record

ArticleCell2016

Epigenetic Activation of WNT5A Drives Glioblastoma Stem Cell Differentiation and Invasive Growth.

Baoli Hu, Qianghu Wang, Y Alan Wang, Sujun Hua, Charles-Etienne Gabriel Sauvé, Derrick Ong, Zheng D Lan, Qing Chang, Yan Wing Ho, Marta Moreno Monasterio and 23 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 178 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
178citing papers in PubMed, 1 pooled it
11.4field-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

178 citing papers in PubMed, 1 synthesis or guideline pooled it, 267 citations in OpenAlex.

  1. Pooled it
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118 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

33 authors at 8 institutions in 3 countries.

Baoli HuDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Qianghu WangDepartment of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; Department of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Y Alan WangDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. Electronic address: yalanwang@mdanderson.org.
Sujun HuaDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Charles-Etienne Gabriel SauvéDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Derrick OngDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Zheng D LanDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Qing ChangDepartment of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; Institute for Applied Cancer Science, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Yan Wing HoDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Marta Moreno MonasterioDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Xin LuDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Yi ZhongDepartment of Epigenetics and Molecular Carcinogenesis, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Jianhua ZhangDepartment of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; Institute for Applied Cancer Science, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Pingna DengDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Zhi TanDepartment of Experimental Therapeutics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Guocan WangDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Wen-Ting LiaoDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Lynda J CorleyDepartment of Pathology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Haiyan YanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Junxia ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Yongping YouDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Ning LiuDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Linbo CaiDepartment of Oncology, Guangdong 999 Brain Hospital, Guangzhou 510510, China.
Gaetano FinocchiaroUnit of Molecular Neuro-Oncology, Fondazione IRCCS Istituto Neurologico C. Besta, 20133 Milano, Italy.
Joanna J PhillipsDepartments of Neurological Surgery and Pathology, University of California, San Francisco, San Francisco, CA 94143, USA.
Mitchel S BergerNeurological Surgery, University of California, San Francisco, San Francisco, CA 94143, USA.
Denise J SpringDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Jian HuDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Erik P SulmanDepartment of Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Gregory N FullerDepartment of Pathology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Lynda ChinDepartment of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Roeland G W VerhaakDepartment of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; Department of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Ronald A DePinhoDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. Electronic address: rdepinho@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USJiangsu Province Hospital · CNNanjing Medical University · CNDana-Farber Cancer Institute · USFondazione IRCCS Istituto Neurologico Carlo Besta · ITGuangdong 999 Brain Hospital · CNNeurological Surgery · USUniversity of California, San Francisco · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Tissue CoreP50CA097257 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joseph F Costello · 2002 to 2026
$57.4M
Tropism Enhanced Oncolytic Adenovirus for the Treatment of Brain TumorsP50CA127001 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Juan Fueyo · 2008 to 2026
$41.2M
Transgenic Mouse and Biobank CoreP01CA095616 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BRENNAN, CAMERON · 2003 to 2012
$20.3M
MDSC-Tumor Crosstalk in Prostate Cancer Progression and Castration ResistanceR00CA194289 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WANG, GUOCAN · 2018 to 2020
$702k
MDSC-tumor crosstalk in prostate cancer progression and castration resistanceK99CA194289 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WANG, GUOCAN · 2016 to 2017
$209k
NCI NIH HHS K99 CA194289NCI NIH HHS P01 CA095616NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA097257NCI NIH HHS P50 CA127001NCI NIH HHS R00 CA194289
6 · The paper itself

Abstract

Glioblastoma stem cells (GSCs) are implicated in tumor neovascularization, invasiveness, and therapeutic resistance. To illuminate mechanisms governing these hallmark features, we developed a de novo glioblastoma multiforme (GBM) model derived from immortalized human neural stem/progenitor cells (hNSCs) to enable precise system-level comparisons of pre-malignant and oncogene-induced malignant states of NSCs. Integrated transcriptomic and epigenomic analyses uncovered a PAX6/DLX5 transcriptional program driving WNT5A-mediated GSC differentiation into endothelial-like cells (GdECs). GdECs recruit existing endothelial cells to promote peritumoral satellite lesions, which serve as a niche supporting the growth of invasive glioma cells away from the primary tumor. Clinical data reveal higher WNT5A and GdECs expression in peritumoral and recurrent GBMs relative to matched intratumoral and primary GBMs, respectively, supporting WNT5A-mediated GSC differentiation and invasive growth in disease recurrence. Thus, the PAX6/DLX5-WNT5A axis governs the diffuse spread of glioma cells throughout the brain parenchyma, contributing to the lethality of GBM.

Indexed as

Endothelial CellsEpigenomicsGene Expression Regulation, NeoplasticGlioblastomaHomeodomain ProteinsHumansNeoplasm InvasivenessNeural Stem CellsPAX6 Transcription FactorProto-Oncogene Proteins c-aktTranscription FactorsWnt-5a ProteinDLX5 protein, humanHomeodomain ProteinsPAX6 protein, humanPAX6 Transcription FactorProto-Oncogene Proteins c-aktTranscription FactorsWnt-5a ProteinWNT5A protein, humancancer stem cell differentiationglioblastomarecurrencetumor microenvironment

Identifiers

PMID27863244
PMCPMC5320931
OpenAlexW2555009198

What OpenQuestion holds

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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.