Evidence map›Paper›PMID 31919052›Full record

ArticleCancer discovery2020

Circadian Regulator CLOCK Recruits Immune-Suppressive Microglia into the GBM Tumor Microenvironment.

Peiwen Chen, Wen-Hao Hsu, Andrew Chang, Zhi Tan, Zhengdao Lan, Ashley Zhou, Denise J Spring, Frederick F Lang, Y Alan Wang, Ronald A DePinho

Open access · greenAbstract read
In one paragraph

Article in Cancer discovery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 156 papers.

0numbers the graph read from it
0cells of the map it votes in
156citing papers in PubMed
10.6field-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

156 citing papers in PubMed, 210 citations in OpenAlex.

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

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

10 authors at 1 institution in 1 country.

Peiwen ChenDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Wen-Hao HsuDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Andrew ChangDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Zhi TanDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Zhengdao LanDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Ashley ZhouDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Denise J SpringDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID https://orcid.org/0000-0002-4593-0901
Frederick F LangDepartment of Neurosurgery and Brain Tumor Center, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Y Alan WangDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas. rdepinho@mdanderson.org yalanwang@mdanderson.org.
Ronald A DePinhoDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas. rdepinho@mdanderson.org yalanwang@mdanderson.org.ORCID https://orcid.org/0000-0002-5625-577X
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
The RAS and P13K Pathways in Pancreatic AdenocarcinomaP01CA117969 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DEPINHO, RONALD ANTHONY · 2006 to 2025
$41.7M
TELOMERASE IN DEVELOPMENT, SENESCENCE AND NEOPLASIAR01CA084628 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DEPINHO, RONALD ANTHONY · 2000 to 2019
$10.5M
Developing Novel Therapeutic Approaches Targeting Macrophages in GBMR01CA231349 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WANG, Y. ALAN · 2019 to 2024
$1.8M
NCI NIH HHS P01 CA117969NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA084628NCI NIH HHS R01 CA231349
6 · The paper itself

Abstract

Glioblastoma (GBM) is a lethal brain tumor containing a subpopulation of glioma stem cells (GSC). Pan-cancer analyses have revealed that stemness of cancer cells correlates positively with immunosuppressive pathways in many solid tumors, including GBM, prompting us to conduct a gain-of-function screen of epigenetic regulators that may influence GSC self-renewal and tumor immunity. The circadian regulator

Indexed as

AnimalsARNTL Transcription FactorsCell Line, TumorCell Self RenewalCLOCK ProteinsGene Expression Regulation, NeoplasticGlioblastomaGlycoproteinsHeterograftsHumansImmunity, CellularIntercellular Signaling Peptides and ProteinsMiceMicrogliaNeoplastic Stem CellsTumor MicroenvironmentARNTL Transcription FactorsBMAL1 protein, humanCLOCK protein, humanCLOCK ProteinsGlycoproteinsIntercellular Signaling Peptides and ProteinsOLFML3 protein, human

Identifiers

PMID31919052
PMCPMC7058515
OpenAlexW2999304067

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.