Genomic and expression analysis of the 8p11-12 amplicon in human breast cancer cell lines

被引:105
作者
Ray, ME
Yang, ZQ
Albertson, D
Kleer, CG
Washburn, JG
Macoska, JA
Ethier, SP
机构
[1] Univ Michigan, Sch Med, Dept Radiat Oncol, Ann Arbor, MI USA
[2] Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI USA
[3] Univ Michigan, Sch Med, Ctr Comprehens Canc, Ann Arbor, MI USA
[4] Univ Calif San Francisco, Canc Res Inst, San Francisco, CA 94143 USA
关键词
D O I
10.1158/0008-5472.CAN-03-1022
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gene amplification is an important mechanism of oncogene activation in breast and other cancers. Characterization of amplified regions of the genome in breast cancer has led to the identification of important oncogenes including erbB-2/HER-2, C-MYC, and fibroblast growth factor receptor (FGFR) 2. Chromosome 8p11-p12 is amplified in 10-15% of human breast cancers. The putative oncogene FGFR1 localizes to this region; however, we show evidence that FGFR inhibition fails to slow growth of three breast cancer cell lines with 8p11-p12 amplification. We present a detailed analysis of this amplicon in three human breast cancer cell lines using comparative genomic hybridization, traditional Southern and Northern analysis, and chromosome 8 cDNA microarray expression profiling. This study has identified new candidate oncogenes within the 8p11-p12 region, supporting the hypothesis that genes other than FGFR1 may contribute to oncogenesis in breast cancers with proximal 8p amplification.
引用
收藏
页码:40 / 47
页数:8
相关论文
共 52 条
  • [1] ADNANE J, 1991, ONCOGENE, V6, P659
  • [2] Anbazhagan R, 1998, AM J PATHOL, V152, P815
  • [3] BERNASCONI R, 1992, PHARM COMMUN, V2, P28
  • [4] INVIVO AMPLIFICATION AND REARRANGEMENT OF C-MYC ONCOGENE IN HUMAN-BREAST TUMORS
    BONILLA, M
    RAMIREZ, M
    LOPEZCUETO, J
    GARIGLIO, P
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1988, 80 (09) : 665 - 671
  • [5] Haploinsufficiency and reduced expression of genes localized to the 8p chromosomal region in human prostate tumors
    Chaib, H
    MacDonald, JW
    Vessella, RL
    Washburn, JG
    Quinn, JE
    Odman, A
    Rubin, MA
    Macoska, JA
    [J]. GENES CHROMOSOMES & CANCER, 2003, 37 (03) : 306 - 313
  • [6] AZU-1:: A candidate breast tumor suppressor and biomarker for tumor progression
    Chen, HM
    Schmeichel, KL
    Mian, IS
    Lelièvre, S
    Petersen, OW
    Bissell, MJ
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (04) : 1357 - 1367
  • [7] Amplification of c-myc gene and overexpression of c-Myc protein in breast cancer and adjacent non-neoplastic tissue
    Chrzan, P
    Skokowski, J
    Karmolinski, A
    Pawelczyk, T
    [J]. CLINICAL BIOCHEMISTRY, 2001, 34 (07) : 557 - 562
  • [8] Cloning of TC-1 (C8orf4), a novel gene found to be overexpressed in thyroid cancer
    Chua, EL
    Young, L
    Wu, WM
    Turtle, JR
    Dong, QH
    [J]. GENOMICS, 2000, 69 (03) : 342 - 347
  • [9] Positional cloning of ZNF217 and NABC1:: Genes amplified at 20q13.2 and overexpressed in breast carcinoma
    Collins, C
    Rommens, JM
    Kowbel, D
    Godfrey, T
    Tanner, M
    Hwang, S
    Polikoff, D
    Nonet, G
    Cochran, J
    Myambo, K
    Jay, KE
    Froula, J
    Cloutier, T
    Kuo, WL
    Yaswen, P
    Dairkee, S
    Giovanola, J
    Hutchinson, GB
    Isola, J
    Kallioniemi, OP
    Palazzolo, M
    Martin, C
    Ericsson, C
    Pinkel, D
    Albertson, D
    Li, WB
    Gray, JW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) : 8703 - 8708
  • [10] Carcinogenesis and translational controls:: TACC1 is down-regulated in human cancers and associates with mRNA regulators
    Conte, N
    Charafe-Jauffret, E
    Delaval, B
    Adélaïde, J
    Ginestier, C
    Geneix, J
    Isnardon, D
    Jacquemier, J
    Birnbaum, D
    [J]. ONCOGENE, 2002, 21 (36) : 5619 - 5630