Evidence map›Paper›PMID 27456282›Full record

ArticleScientific reports2016

ABCG2 regulates self-renewal and stem cell marker expression but not tumorigenicity or radiation resistance of glioma cells.

Boyoung Wee, Alexander Pietras, Tatsuya Ozawa, Elena Bazzoli, Ondrej Podlaha, Christophe Antczak, Bengt Westermark, Sven Nelander, Lene Uhrbom, Karin Forsberg-Nilsson and 3 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 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.9field-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

35 citing papers in PubMed, 54 citations in OpenAlex.

  1. International journal of molecular sciences · 2026
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  8. Antiproliferative Activity ofCombinatorial chemistry & high throughput screening · 2025
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  13. Glioblastoma Stem Cells-Useful Tools in the Battle against Cancer.International journal of molecular sciences · 2022
    Review
  14. GZ17-6.02 Inhibits the Growth of EGFRvIII+ Glioblastoma.International journal of molecular sciences · 2022
    Article
  15. Review
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  17. Review
  18. Article
  19. Review
  20. Review
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

13 authors at 8 institutions in 3 countries.

Boyoung WeeCancer Biology and Genetics Program, New York, NY 10021, USA.
Alexander PietrasHuman Biology Division, Solid Tumor and Translational Research, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Tatsuya OzawaHuman Biology Division, Solid Tumor and Translational Research, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Elena BazzoliCentro San Giovanni di Dio - Fatebenefratelli, IRCCS, 25123 Bs, Italy.
Ondrej PodlahaDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Christophe AntczakHTS Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY 10021, USA.
Bengt WestermarkDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Rudbeck Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
Sven NelanderDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Rudbeck Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
Lene UhrbomDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Rudbeck Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
Karin Forsberg-NilssonDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Rudbeck Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
Hakim DjaballahHTS Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY 10021, USA.
Franziska MichorDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Eric C HollandHuman Biology Division, Solid Tumor and Translational Research, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Science for Life Laboratory · SEFred Hutch Cancer Center · USHarvard University · USMemorial Sloan Kettering Cancer Center · USCancer Genetics (United States) · USIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Washington · USUppsala University · SE

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
The Cell-Of-Origin of Human CancersU54CA143798 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI MICHOR, FRANZISKA · 2009 to 2014
$11.2M
The Proneural Perivascular Niche and Therapeutic ResponseU54CA163167 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI HOLLAND, ERIC C. · 2011 to 2015
$4.6M
P3IK Signaling and Biology of Therapeutic Response in Brain and Prostate TumorsU01CA141502 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI HOLLAND, ERIC C. · 2009 to 2013
$4.2M
Modeling the effects of INK4 alpha ARF loss on gliomasR01CA094842 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI HOLLAND, ERIC C · 2001 to 2003
$771k
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA094842NCI NIH HHS U01 CA141502NCI NIH HHS U54 CA143798NCI NIH HHS U54 CA163167
6 · The paper itself

Abstract

Glioma cells with stem cell traits are thought to be responsible for tumor maintenance and therapeutic failure. Such cells can be enriched based on their inherent drug efflux capability mediated by the ABC transporter ABCG2 using the side population assay, and their characteristics include increased self-renewal, high stem cell marker expression and high tumorigenic capacity in vivo. Here, we show that ABCG2 can actively drive expression of stem cell markers and self-renewal in glioma cells. Stem cell markers and self-renewal was enriched in cells with high ABCG2 activity, and could be specifically inhibited by pharmacological and genetic ABCG2 inhibition. Importantly, despite regulating these key characteristics of stem-like tumor cells, ABCG2 activity did not affect radiation resistance or tumorigenicity in vivo. ABCG2 effects were Notch-independent and mediated by diverse mechanisms including the transcription factor Mef. Our data demonstrate that characteristics of tumor stem cells are separable, and highlight ABCG2 as a potential driver of glioma stemness.

Indexed as

AnimalsATP Binding Cassette Transporter, Subfamily G, Member 2Biomarkers, TumorBrain NeoplasmsCell Line, TumorGene Expression Regulation, NeoplasticGliomaHumansMiceNeoplasm ProteinsNeoplasm TransplantationNeoplastic Stem CellsRadiation ToleranceReceptors, NotchSignal TransductionUp-RegulationABCG2 protein, humanATP Binding Cassette Transporter, Subfamily G, Member 2Biomarkers, TumorNeoplasm ProteinsReceptors, Notch

Identifiers

PMID27456282
PMCPMC4960591
OpenAlexW2488777145

What OpenQuestion holds

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LicenceCC BY
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.