Article (Scientific journals)
Monosomy of chromosome 10 associated with dysregulation of epidermal growth factor signaling in glioblastomas.
Yadav, Ajay K; Renfrow, Jaclyn J; Scholtens, Denise M et al.
2009In JAMA: Journal of the American Medical Association, 302 (3), p. 276-89
Peer Reviewed verified by ORBi
 

Files


Full Text
9-Monosomy-Robe.pdf
Publisher postprint (513.92 kB)
Request a copy

All documents in ORBi are protected by a user license.

Send to



Details



Keywords :
Annexin A7/genetics/metabolism; Brain Neoplasms/genetics/metabolism/mortality; Cell Line, Tumor; Cell Transformation, Neoplastic/genetics; Chromosomes, Human, Pair 10/genetics; Chromosomes, Human, Pair 7; Epidermal Growth Factor/metabolism; Epigenesis, Genetic; Female; Gene Deletion; Gene Dosage; Gene Expression; Gene Expression Regulation, Neoplastic; Gene Knockdown Techniques; Genes, Tumor Suppressor; Glioblastoma/genetics/metabolism/mortality; Humans; Loss of Heterozygosity; Male; Middle Aged; Monosomy; Mutation; PTEN Phosphohydrolase/genetics; RNA, Messenger/analysis; Receptor, Epidermal Growth Factor/genetics/metabolism; Signal Transduction; Survival Analysis
Abstract :
[en] CONTEXT: Glioblastomas--uniformly fatal brain tumors--often have both monosomy of chromosome 10 and gains of the epidermal growth factor receptor (EGFR) gene locus on chromosome 7, an association for which the mechanism is poorly understood. OBJECTIVES: To assess whether coselection of EGFR gains on 7p12 and monosomy 10 in glioblastomas promotes tumorigenic epidermal growth factor (EGF) signaling through loss of the annexin A7 (ANXA7) gene on 10q21.1-q21.2 and whether ANXA7 acts as a tumor suppressor gene by regulating EGFR in glioblastomas. DESIGN, SETTING, AND PATIENTS: Multidimensional analysis of gene, coding sequence, promoter methylation, messenger RNA (mRNA) transcript, protein data for ANXA7 (and EGFR), and clinical patient data profiles of 543 high-grade gliomas from US medical centers and The Cancer Genome Atlas pilot project (made public 2006-2008; and unpublished, tumors collected 2001-2008). Functional analyses using LN229 and U87 glioblastoma cells. MAIN OUTCOME MEASURES: Associations among ANXA7 gene dosage, coding sequence, promoter methylation, mRNA transcript, and protein expression. Effect of ANXA7 haploinsufficiency on EGFR signaling and patient survival. Joint effects of loss of ANXA7 and gain of EGFR expression on tumorigenesis. RESULTS: Heterozygous ANXA7 gene deletion is associated with significant loss of ANXA7 mRNA transcript expression (P = 1 x 10(-15); linear regression) and a reduction (mean [SEM]) of 91.5% (2.3%) of ANXA7 protein expression compared with ANXA7 wild-type glioblastomas (P = .004; unpaired t test). ANXA7 loss of function stabilizes the EGFR protein (72%-744% increase in EGFR protein abundance) and augments EGFR transforming signaling in glioblastoma cells. ANXA7 haploinsufficiency doubles tumorigenic potential of glioblastoma cells, and combined ANXA7 knockdown and EGFR overexpression promotes tumorigenicity synergistically. The heterozygous loss of ANXA7 in approximately 75% of glioblastomas in the The Cancer Genome Atlas plus infrequency of ANXA7 mutation (approximately 6% of tumors) indicates its role as a haploinsufficiency gene. ANXA7 mRNA transcript expression, dichotomized at the median, associates with patient survival in 191 glioblastomas (log-rank P = .008; hazard ratio [HR], 0.667; 95% confidence interval [CI], 0.493-0.902; 46.9 vs 74.8 deaths/100 person-years for high vs low ANXA7 mRNA expression) and with a separate group of 180 high-grade gliomas (log-rank P = .00003; HR, 0.476; 95% CI, 0.333-0.680; 21.8 vs 50.0 deaths/100 person-years for high vs low ANXA7 mRNA expression). Deletion of the ANXA7 gene associates with poor patient survival in 189 glioblastomas (log-rank P = .042; HR, 0.686; 95% CI, 0.476-0.989; 54.0 vs 80.1 deaths/100 person-years for wild-type ANXA7 vs ANXA7 deletion). CONCLUSION: Haploinsufficiency of the tumor suppressor ANXA7 due to monosomy of chromosome 10 provides a clinically relevant mechanism to augment EGFR signaling in glioblastomas beyond that resulting from amplification of the EGFR gene.
Disciplines :
Genetics & genetic processes
Author, co-author :
Yadav, Ajay K
Renfrow, Jaclyn J
Scholtens, Denise M
Xie, Hehuang
Duran, George E
Bredel, Claudia
Vogel, Hannes
Chandler, James P
Chakravarti, Arnab
Robe, Pierre ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > GIGA-R : Génétique générale et humaine - Département des sciences biomédicales et précliniques
Das, Sunit
Scheck, Adrienne C
Kessler, John A
Soares, Marcelo B
Sikic, Branimir I
Harsh, Griffith R
Bredel, Markus
More authors (7 more) Less
Language :
English
Title :
Monosomy of chromosome 10 associated with dysregulation of epidermal growth factor signaling in glioblastomas.
Publication date :
2009
Journal title :
JAMA: Journal of the American Medical Association
ISSN :
0098-7484
eISSN :
1538-3598
Publisher :
American Medical Association, Chicago, United States - Illinois
Volume :
302
Issue :
3
Pages :
276-89
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 24 February 2010

Statistics


Number of views
72 (1 by ULiège)
Number of downloads
0 (0 by ULiège)

Scopus citations®
 
59
Scopus citations®
without self-citations
53
OpenCitations
 
43

Bibliography


Similar publications



Contact ORBi