Evidence map›Paper›PMID 20657792›Full record

ArticleGenes & cancer2010

Erythropoietin Receptor Signaling Through STAT3 Is Required For Glioma Stem Cell Maintenance.

Yiting Cao, Justin D Lathia, Christine E Eyler, Qiulian Wu, Zhizhong Li, Hui Wang, Roger E McLendon, Anita B Hjelmeland, Jeremy N Rich

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Genes & cancer, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06991101 (Randomized Phase 2 Trial of Ruxolitinib in Combination With Radiation and Temozolomide Compared to Radiation and Temozolomide for Newly Diagnosed Glioblastoma.), which is not on this map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.2field-weighted citation impact, top 6% 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.

NCT06991101 phase2recruitingnot on this mapstarted 2025, after this paper: background citation

Randomized Phase 2 Trial of Ruxolitinib in Combination With Radiation and Temozolomide Compared to Radiation and Temozolomide for Newly Diagnosed Glioblastoma.

TypeinterventionalSponsorBaptist Health South FloridaRan2025 to 2030Enrolled190ConditionsGlioblastoma, Brain Cancer, Glioblastoma Multiforme, Glioblastoma Multiforme of BrainArmsRuxolitinib, Temozolomide, Radiation Therapy
3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 82 citations in OpenAlex.

  1. Review
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  3. Article
  4. Review
  5. Erythroid Cells as Full Participants in the Tumor Microenvironment.International journal of molecular sciences · 2023
    Review
  6. Article
  7. Review
  8. Review
  9. Review
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  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Overcoming therapeutic resistance in glioblastoma: the way forward.The Journal of clinical investigation · 2017
    Review
  18. Article
  19. Article
  20. Article
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

9 authors at 6 institutions in 1 country.

Yiting CaoDepartment of Surgery, Duke University Medical Center, Durham, North Carolina 27705.
Justin D Lathia
Christine E Eyler
Qiulian Wu
Zhizhong Li
Hui Wang
Roger E McLendon
Anita B Hjelmeland
Jeremy N Rich
Cleveland Clinic · USCleveland Clinic Lerner College of Medicine · USDuke University · USCase Comprehensive Cancer CenterDuke Medical Center · USDuke University Hospital · US

Funding

Stem Cell-Like Glioma Cells in AngiogenesisR01CA129958 · NCI · DUKE UNIVERSITY · PI RICH, JEREMY N · 2008 to 2012
$1.6M
TGFbeta-PTEN Interactions in Glioma Biology & TherapyR01CA116659 · NCI · DUKE UNIVERSITY · PI RICH, JEREMY N · 2006 to 2010
$1.4M
Molecular Mechanisms of SPARC Mediated Glioma InvasionR01NS054276 · NINDS · DUKE UNIVERSITY · PI RICH, JEREMY N · 2006 to 2010
$1.2M
The Roles of Osteonectin and Osteoactivin in GliomasK02NS047409 · NINDS · DUKE UNIVERSITY · PI RICH, JEREMY N. · 2004 to 2007
$612k
Integrin regulation of brain tumor initiating cellsF32CA142159 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI LATHIA, JUSTIN D. · 2009 to 2011
$98k
Targeting Brain Tumor Stem CellsF30NS063496 · NINDS · DUKE UNIVERSITY · PI EYLER, CHRISTINE ELISSA · 2009 to 2010
$61k
NCI NIH HHS F32 CA142159NCI NIH HHS R01 CA116659NCI NIH HHS R01 CA129958NINDS NIH HHS F30 NS063496NINDS NIH HHS K02 NS047409NINDS NIH HHS R01 NS054276
6 · The paper itself

Abstract

Recombinant erythropoietin (EPO) is a growth factor used in the treatment of chemotherapy-induced anemia, but recent studies suggest that EPO may accelerate cancer growth. Although several cancers express EPO receptors (EPORs), the mechanism by which EPOR promotes tumor growth remains poorly understood. Glioblastomas display a cellular hierarchy of self-renewal and tumor propagation restricted to glioma stem cells (GSCs). We find that GSCs express higher levels of EPOR than matched non-stem glioma cells. Prospective enrichment for EPOR on GSCs increased neurosphere formation, suggesting that EPOR can select for a subset of GSCs with increased self-renewal capacity. Targeting EPOR expression with lentiviral mediated short hairpin RNA (shRNA) reduced GSC growth, survival, and neurosphere formation capacity, defining a crucial role for EPOR in GSC maintenance. We further find that STAT3 is an important mediator of EPOR signals in GSCs. EPOR knockdown attenuated the basal activation of STAT3 present in GSCs, and a small molecule inhibitor of STAT3 reduced GSC growth and survival. EPOR signaling was critical for survival in vivo, as targeting EPOR expression decreased GSC tumorigenic potential. Elevated EPOR expression also associated with poor patient outcome. Thus, EPOR on GSCs promotes tumor growth and may explain the poor survival of cancer patients treated with EPO.

Identifiers

PMID20657792
PMCPMC2906804
OpenAlexW2020510601

What OpenQuestion holds

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Registered trials

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.