Evidence map›Paper›PMID 22869205›Full record

ArticleOncotarget2012

Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas.

Yuchen Jiao, Patrick J Killela, Zachary J Reitman, Ahmed B Rasheed, Christopher M Heaphy, Roeland F de Wilde, Fausto J Rodriguez, Sergio Rosemberg, Sueli Mieko Oba-Shinjo, Suely Kazue Nagahashi Marie and 19 more

Open access · hybridAbstract read
In one paragraph

Article in Oncotarget, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 324 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
324citing papers in PubMed, 3 pooled it
30.2field-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

324 citing papers in PubMed, 3 syntheses or guidelines pooled it, 577 citations in OpenAlex.

  1. Pooled it
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  15. Significance ofClinical Medicine Insights. Oncology · 2025
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. IDH mutant high-grade gliomas.Frontiers in molecular neuroscience · 2025
    Review

264 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

29 authors at 8 institutions in 2 countries.

Yuchen JiaoLudwig Center for Cancer Genetics and Howard Hughes Medical Institutions, The Johns Hopkins Kimmel Cancer Center, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA.
Patrick J Killela
Zachary J Reitman
Ahmed B Rasheed
Christopher M Heaphy
Roeland F de Wilde
Fausto J Rodriguez
Sergio Rosemberg
Sueli Mieko Oba-Shinjo
Suely Kazue Nagahashi Marie
Chetan Bettegowda
Nishant Agrawal
Eric Lipp
Christopher Pirozzi
Giselle Lopez
Yiping He
Henry Friedman
Allan H Friedman
Gregory J Riggins
Matthias Holdhoff
Peter Burger
Roger McLendon
Darell D Bigner
Bert Vogelstein
Alan K Meeker
Kenneth W Kinzler
Nickolas Papadopoulos
Luis A Diaz
Hai Yan
Cancer Genetics (United States) · USDuke University Hospital · USSidney Kimmel Cancer Center · USDuke Medical Center · USPediatric Brain Tumor Foundation · USUniversidade de São Paulo · BRJohns Hopkins University · USSwim Across America · US

Funding

TUMOR SUPPRESSOR GENES IN HUMAN MEDULLOBLASTOMAP50NS020023 · NINDS · DUKE UNIVERSITY · PI ZALUTSKY, MICHAEL ROD · 1985 to 2013
$17.3M
BRAIN TUMORS: IMMUNOLOGICAL AND BIOLOGICAL STUDIESR37CA011898 · NCI · DUKE UNIVERSITY · PI BIGNER, DARELL D · 1988 to 2012
$8.1M
MOLECULAR GENETIC ANALYSIS OF COLORECTAL CANCERR37CA043460 · NCI · JOHNS HOPKINS UNIVERSITY · PI VOGELSTEIN, BERT · 1997 to 2016
$7.4M
Genes from the FAP LocusR37CA057345 · NCI · JOHNS HOPKINS UNIVERSITY · PI KINZLER, KENNETH W. · 2002 to 2016
$7.4M
The Role of IDH1 Mutations in Gliomagenesis and MetabolismR01CA140316 · NCI · DUKE UNIVERSITY · PI YAN, HAI · 2010 to 2019
$3.2M
Phase I study of Clostridium novyi-NT spores in solid tumor cancer patientsR01CA129825 · NCI · JOHNS HOPKINS UNIVERSITY · PI DIAZ, LUIS A · 2007 to 2010
$1.2M
GENES FROM THE FAP LOCUSR01CA057345 · NCI · JOHNS HOPKINS UNIVERSITY · PI KINZLER, KENNETH W. · 1992 to 2001
$734k
Howard Hughes Medical InstituteNCI NIH HHS 5P50 CA108785NCI NIH HHS 5R01-CA140316NCI NIH HHS CA057345,NCI NIH HHS CA129825NCI NIH HHS R01 CA057345NCI NIH HHS R01 CA129825NCI NIH HHS R01 CA140316NCI NIH HHS R37 CA 011898NCI NIH HHS R37 CA043460NCI NIH HHS R37 CA057345NINDS NIH HHS 5P50 NS20023NINDS NIH HHS P50 NS020023
6 · The paper itself

Abstract

Mutations in the critical chromatin modifier ATRX and mutations in CIC and FUBP1, which are potent regulators of cell growth, have been discovered in specific subtypes of gliomas, the most common type of primary malignant brain tumors. However, the frequency of these mutations in many subtypes of gliomas, and their association with clinical features of the patients, is poorly understood. Here we analyzed these loci in 363 brain tumors. ATRX is frequently mutated in grade II-III astrocytomas (71%), oligoastrocytomas (68%), and secondary glioblastomas (57%), and ATRX mutations are associated with IDH1 mutations and with an alternative lengthening of telomeres phenotype. CIC and FUBP1 mutations occurred frequently in oligodendrogliomas (46% and 24%, respectively) but rarely in astrocytomas or oligoastrocytomas ( more than 10%). This analysis allowed us to define two highly recurrent genetic signatures in gliomas: IDH1/ATRX (I-A) and IDH1/CIC/FUBP1 (I-CF). Patients with I-CF gliomas had a significantly longer median overall survival (96 months) than patients with I-A gliomas (51 months) and patients with gliomas that did not harbor either signature (13 months). The genetic signatures distinguished clinically distinct groups of oligoastrocytoma patients, which usually present a diagnostic challenge, and were associated with differences in clinical outcome even among individual tumor types. In addition to providing new clues about the genetic alterations underlying gliomas, the results have immediate clinical implications, providing a tripartite genetic signature that can serve as a useful adjunct to conventional glioma classification that may aid in prognosis, treatment selection, and therapeutic trial design.

Indexed as

MutationAdultBrain NeoplasmsDNA-Binding ProteinsDNA HelicasesFemaleGene SilencingGliomaHumansImmunohistochemistryIsocitrate DehydrogenaseMaleNeoplasm GradingNuclear ProteinsPrognosisRepressor ProteinsATRX protein, humanCIC protein, humanDNA-Binding ProteinsDNA HelicasesFUBP1 protein, humanIDH1 protein, humanIsocitrate DehydrogenaseNuclear ProteinsRepressor ProteinsRNA-Binding ProteinsX-linked Nuclear Protein

Identifiers

PMID22869205
PMCPMC3443254
OpenAlexW1921809757

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.