Gene expression profiles associated with treatment response in oligodendrogliomas

被引:101
作者
French, PJ
Swagemakers, SMA
Nagel, JHA
Kouwenhoven, MCM
Brouwer, E
van der Spek, P
Luider, TM
Kros, JM
van den Bent, MJ
Smitt, PAS
机构
[1] Erasmus MC, Josephine Nefkens Inst, Canc Genom Ctr, Dept Neurol, NL-3000 DR Rotterdam, Netherlands
[2] Erasmus MC, Canc Genom Ctr, Dept Bioinformat, NL-3000 DR Rotterdam, Netherlands
[3] Erasmus MC, Canc Genom Ctr, Dept Pathol, NL-3000 DR Rotterdam, Netherlands
[4] Erasmus MC, Canc Genom Ctr, Dept Med Oncol, NL-3000 DR Rotterdam, Netherlands
[5] Erasmus MC, Canc Genom Ctr, Dept Cell Biol & Genet, NL-3000 DR Rotterdam, Netherlands
关键词
D O I
10.1158/0008-5472.CAN-05-1886
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oligodendrogliomas are a specific subtype of brain tumor of which the majority responds favorably to chemotherapy. In this study, we made use of expression profiling to identify chemosensitive oligodendroglial tumors. Correlation of expression profiles to loss of heterozygosity on 1p and 19q, common chromosomal aberrations associated with response to treatment, identified 376, 64, and 60 differentially expressed probe sets associated with loss of 1p, 19q or 1p, and 19q, respectively. Correlation of expression profiles to the tumors' response to treatment identified 16 differentially expressed probe sets. Because transcripts associated with chemotherapeutic response were identified independent of common chromosomal aberrations, expression profiling may be used as an alternative approach to the tumors' 1p status to identify chemosensitive oligodendroglial tumors. Finally, we correlated expression profiles to survival of the patient after diagnosis and identified 103 differentially expressed probe sets. The observation that many genes are differentially expressed between long and short survivors indicates that the genetic background of the tumor is an important factor in determining the prognosis of the patient. Furthermore, these transcripts can help identify patient subgroups that are associated with favorable prognosis. Our study is the first to correlate gene expression with chromosomal aberrations and clinical performance (response to treatment and survival) in oligodendrogliomas. The differentially expressed transcripts can help identify patient subgroups with good prognosis and those that will benefit from chemotherapeutic treatments.
引用
收藏
页码:11335 / 11344
页数:10
相关论文
共 54 条
[11]   ARH is a modular adaptor protein that interacts with the LDL receptor, clathrin, and AP-2 [J].
He, GC ;
Gupta, S ;
Yi, M ;
Michaely, P ;
Hobbs, HH ;
Cohen, JC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (46) :44044-44049
[12]   Galectin-9 in physiological and pathological conditions [J].
Hirashima, M ;
Kashio, Y ;
Nishi, N ;
Yamauchi, A ;
Imaizumi, T ;
Kageshita, T ;
Saita, N ;
Nakamura, T .
GLYCOCONJUGATE JOURNAL, 2002, 19 (7-9) :593-600
[13]   Molecular heterogeneity of oligodendrogliomas suggests alternative pathways in tumor progression [J].
Hoang-Xuan, K ;
He, J ;
Huguet, S ;
Mokhtari, K ;
Marie, Y ;
Kujas, M ;
Leuraud, P ;
Capelle, L ;
Delattre, JY ;
Poirier, J ;
Broët, P ;
Sanson, M .
NEUROLOGY, 2001, 57 (07) :1278-1281
[14]   Gene expression profiling and subgroup identification of oligodendrogliomas [J].
Huang, H ;
Okamoto, Y ;
Yokoo, H ;
Heppner, FL ;
Vital, A ;
Fevre-Montange, M ;
Jouvet, A ;
Yonekawa, Y ;
Lazaridis, EN ;
Kleihues, P ;
Ohgaki, H .
ONCOGENE, 2004, 23 (35) :6012-6022
[15]  
Ino Y, 2001, CLIN CANCER RES, V7, P839
[16]  
INOSTROZA JA, 1992, CELL, V70, P477
[17]   Molecular pathogenesis of oligodendroglial tumors [J].
Jeuken, JWM ;
von Deimling, A ;
Wesseling, P .
JOURNAL OF NEURO-ONCOLOGY, 2004, 70 (02) :161-181
[18]   Progress in long-term survival in adult patients with supratentorial low-grade gliomas: a population-based study of 993 patients in whom tumors were diagnosed between 1970 and 1993 [J].
Johannesen, TB ;
Langmark, F ;
Lote, K .
JOURNAL OF NEUROSURGERY, 2003, 99 (05) :854-862
[19]   Sp1-and Kruppel-like transcription factors [J].
Kaczynski, J ;
Cook, T ;
Urrutia, R .
GENOME BIOLOGY, 2003, 4 (02)
[20]   Decreased expression of the seven ARP2/3 complex genes in human gastric cancers [J].
Kaneda, A ;
Kaminishi, M ;
Sugimura, T ;
Ushijima, T .
CANCER LETTERS, 2004, 212 (02) :203-210