Evidence map›Paper›PMID 28986380›Full record

ArticleCancer research2017

Astrocytes Promote Medulloblastoma Progression through Hedgehog Secretion.

Yongqiang Liu, Larra W Yuelling, Yuan Wang, Fang Du, Renata E Gordon, Jenny A O'Brien, Jessica M Y Ng, Shannon Robins, Eric H Lee, Hailong Liu and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

46 citing papers in PubMed, 70 citations in OpenAlex.

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  12. Medulloblastoma: biology and immunotherapy.Frontiers in immunology · 2025
    Review
  13. Article
  14. Distribution, contribution and regulation of nestinJournal of advanced research · 2024
    Review
  15. Article
  16. Article
  17. Article
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  19. Review
  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

12 authors at 3 institutions in 2 countries.

Yongqiang LiuCancer Biology Program, Fox Chase Cancer Center, Temple University Health System, Philadelphia, Pennsylvania.
Larra W YuellingCancer Biology Program, Fox Chase Cancer Center, Temple University Health System, Philadelphia, Pennsylvania.
Yuan WangLaboratory of Molecular Neuropathology, College of Pharmaceutical Sciences, Soochow University, Suzhou, Jiangsu, China.
Fang DuCancer Biology Program, Fox Chase Cancer Center, Temple University Health System, Philadelphia, Pennsylvania.
Renata E GordonCancer Biology Program, Fox Chase Cancer Center, Temple University Health System, Philadelphia, Pennsylvania.
Jenny A O'BrienCancer Biology Program, Fox Chase Cancer Center, Temple University Health System, Philadelphia, Pennsylvania.
Jessica M Y NgChildren's Research Institute, Children's Mercy Kansas City, Kansas City, Missouri.
Shannon RobinsCancer Biology Program, Fox Chase Cancer Center, Temple University Health System, Philadelphia, Pennsylvania.
Eric H LeeCancer Biology Program, Fox Chase Cancer Center, Temple University Health System, Philadelphia, Pennsylvania.
Hailong LiuCancer Biology Program, Fox Chase Cancer Center, Temple University Health System, Philadelphia, Pennsylvania.
Tom CurranChildren's Research Institute, Children's Mercy Kansas City, Kansas City, Missouri.
Zeng-Jie YangCancer Biology Program, Fox Chase Cancer Center, Temple University Health System, Philadelphia, Pennsylvania. zengjie.yang@fccc.edu.
Temple University Health System · USChildren's Mercy Hospital · USSoochow University · CN

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
TRAINING PROGRAM IN CANCER RESEARCHT32CA009035 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI CHERNOFF, JONATHAN · 1985 to 2020
$10.5M
Leukotriene-Induced Nestin Expression Promotes Medulloblastoma TumorigenesisR01CA178380 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI YANG, ZENG-JIE · 2014 to 2018
$1.9M
(PQD4) MicroRNA Dysregulation in Field Effect is a Prerequisite for TumorigenesisR21CA185504 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI YANG, ZENG-JIE · 2014 to 2015
$427k
NCI NIH HHS P30 CA006927NCI NIH HHS R01 CA178380NCI NIH HHS R21 CA185504NCI NIH HHS T32 CA009035
6 · The paper itself

Abstract

Astrocytes, the most abundant type of glial cells in the brain, play critical roles in supporting neuronal development and brain function. Although astrocytes have been frequently detected in brain tumors, including medulloblastoma (MB), their functions in tumorigenesis are not clear. Here, we demonstrate that astrocytes are essential components of the MB tumor microenvironment. Tumor-associated astrocytes (TAA) secrete the ligand sonic hedgehog (Shh), which is required for maintaining MB cell proliferation despite the absence of its primary receptor Patched-1 (Ptch1). Shh drives expression of Nestin in MB cells through a smoothened-dependent, but Gli1-independent mechanism. Ablation of TAA dramatically suppresses Nestin expression and blocks tumor growth. These findings demonstrate an indispensable role for astrocytes in MB tumorigenesis and reveal a novel Ptch1-independent Shh pathway involved in MB progression.

Indexed as

AnimalsAstrocytesCarcinogenesisCell ProliferationCells, CulturedCerebellar NeoplasmsHedgehog ProteinsMedulloblastomaMiceMice, TransgenicNestinPatched-1 ReceptorSmoothened ReceptorTumor MicroenvironmentZinc Finger Protein GLI1Gli1 protein, mouseHedgehog ProteinsNes protein, mouseNestinPatched-1 ReceptorPtch1 protein, mouseShh protein, mouseSmoothened ReceptorSmo protein, mouseZinc Finger Protein GLI1

Identifiers

PMID28986380
PMCPMC5759326
OpenAlexW2761938825

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.