Real-time quantitative PCR analysis of regions involved in gene amplification reveals gene overdose in low-grade astrocytic gliomas

被引:12
作者
Arjona, D
Bello, MJ
Alonso, ME
Isla, A
De Campos, JM
Vaquero, J
Sarasa, JL
Gutierrez, M
Rey, JA
机构
[1] Hosp Univ La Paz, Lab Oncogenet Mol, Unidad Invest, Madrid 28046, Spain
[2] Hosp Univ La Paz, Lab Secuenciac Automat, Unit Invest, Madrid 28046, Spain
[3] Hosp Univ La Paz, Dept Neurocirugia, Madrid 28046, Spain
[4] Hosp Rio Hortega, Dept Neurocirugia, Valladolid, Spain
[5] Hosp Puerta De Hierro, Dept Neurocirurgia, Madrid, Spain
[6] Fdn Jimenez Diaz, Dept Anat Patol, E-28040 Madrid, Spain
[7] Hosp Univ La Paz, Dept Anat Patol, Madrid 28046, Spain
关键词
astrocytic gliomas; gene amplification; 1q32; region; 12q13;
D O I
10.1097/01.pas.0000177799.58336.1a
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have studied gene amplification of genes located in 1q32 (GAC1, ELF3, MDM4, and ren1), 4q11 (PDGFR-alpha), and in 12q 13-14 (MDM2 and CDK4) using quantitative real-time PCR in a group of 86 tumors consisting of 44 WHO grade IV glioblastomas (GBM) (34 primary and 10 secondary tumors), 21 WHO grade III anaplastic astrocytomas (AA), and 21 WHO grade 11 astrocytomas (All). Gene amplification was present in 56 of the 86 samples (65%) in at least 1 gene in our series. GAC1 (51%) and MDM4 (27%) were the most frequently amplified genes within the 1q32 amplicon, and their higher amplification frequency was statistically significant (P < 0.05, chi(2)) in the low-grade astrocytomas. Concordant coamplification was determined for ELF3 and ren1 or ren1 and MDM4 in the grade III-IV tumors. MDM2 amplification was significantly more frequent in primary GBM (16%) than was in secondary GBM (0%). The present study shows that gene amplification in the studied regions is already present in low-grade astrocytic tumors and that amplification of some genes may represent another molecular marker to differentiate primary from secondary GBM.
引用
收藏
页码:224 / 229
页数:6
相关论文
共 39 条
[11]   GENE AMPLIFICATION IN HUMAN GLIOMAS [J].
COLLINS, VP .
GLIA, 1995, 15 (03) :289-296
[12]   CHROMOSOMAL MAPPING OF HUMAN CDK2, CDK4, AND CDK5 CELL-CYCLE KINASE GENES [J].
DEMETRICK, DJ ;
ZHANG, H ;
BEACH, DH .
CYTOGENETICS AND CELL GENETICS, 1994, 66 (01) :72-74
[13]   Ribosomal 18S RNA prevails over glyceraldehyde-3-phosphate dehydrogenase and β-actin genes as internal standard for quantitative comparison of mRNA levels in invasive and noninvasive human melanoma cell subpopulations [J].
Goidin, D ;
Mamessier, A ;
Staquet, MJ ;
Schmitt, D ;
Berthier-Vergnes, O .
ANALYTICAL BIOCHEMISTRY, 2001, 295 (01) :17-21
[14]  
Gonzalez-Gomez P, 2003, INT J ONCOL, V22, P601
[15]   Microvascular angiogenesis and the renin-angiotensin system [J].
Greene, AS ;
Amaral, SL .
CURRENT HYPERTENSION REPORTS, 2002, 4 (01) :56-62
[16]   EXPRESSION OF PDGF AND PDGF RECEPTORS IN HUMAN ASTROCYTOMA OPERATION SPECIMENS SUPPORTS THE EXISTENCE OF AN AUTOCRINE LOOP [J].
GUHA, A ;
DASHNER, K ;
BLACK, PM ;
WAGNER, JA ;
STILES, CD .
INTERNATIONAL JOURNAL OF CANCER, 1995, 60 (02) :168-173
[17]   Mdm2 promotes the rapid degradation of p53 [J].
Haupt, Y ;
Maya, R ;
Kazaz, A ;
Oren, M .
NATURE, 1997, 387 (6630) :296-299
[18]  
HE J, 1994, CANCER RES, V54, P5804
[19]  
Hermanson M, 1996, CANCER RES, V56, P164
[20]  
Ichimura K, 2000, CANCER RES, V60, P417