CGH microarrays and cancer

被引:75
作者
Kallioniemi, Anne [1 ,2 ]
机构
[1] Univ Tampere, Tampere Univ Hosp, Canc Genet Lab, FI-33014 Tampere, Finland
[2] Univ Tampere, Inst Med Technol, FI-33014 Tampere, Finland
关键词
D O I
10.1016/j.copbio.2007.11.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Genetic alterations are a key feature of cancer cells and typically target biological processes and pathways that contribute to cancer pathogenesis. Array-based comparative genomic hybridization (aCGH) has provided a wealth of new information on copy number changes in cancer on a genome-wide level and aCGH data have also been utilized in cancer classification. More importantly, aCGH analyses have allowed highly accurate localization of specific genetic alterations that, for example, are associated with tumor progression, therapy response, or patient outcome. The genes involved in these aberrations are likely to contribute to cancer pathogenesis, and the high-resolution mapping by aCGH greatly facilitates the subsequent identification of these cancer-associated genes.
引用
收藏
页码:36 / 40
页数:5
相关论文
共 52 条
[1]   Array comparative genomic hybridization analysis of chromosomal imbalances and their target genes in gastrointestinal stromal tumors [J].
Assamaki, Reetta ;
Sarlomo-Rilkala, Marit ;
Lopez-Guerrero, Jose Antonio ;
Lasota, Jerzy ;
Andersson, Leif C. ;
Llombart-Bosch, Antonio ;
Miettinen, Markku ;
Knuutila, Sakari .
GENES CHROMOSOMES & CANCER, 2007, 46 (06) :564-576
[2]   Identification of limited regions of genetic aberrations in patients affected with Wilms' tumor using a tiling-path chromosome 22 array [J].
Benetkiewicz, M ;
de Ståhl, TD ;
Gördör, A ;
Pfeifer, S ;
Wittmann, S ;
Gessler, M ;
Dumanski, JP .
INTERNATIONAL JOURNAL OF CANCER, 2006, 119 (03) :571-578
[3]   Distinct patterns of DNA copy number alteration are associated with different clinicopathological features and gene-expression subtypes of breast cancer [J].
Bergamaschi, Anna ;
Kim, Young H. ;
Wang, Pei ;
Sorlie, Therese ;
Hernandez-Boussard, Tina ;
Lonning, Per E. ;
Tibshirani, Robert ;
Borresen-Dale, Anne-Lise ;
Pollack, Jonathan R. .
GENES CHROMOSOMES & CANCER, 2006, 45 (11) :1033-1040
[4]   High-resolution mapping of genomic imbalance and identification of gene expression profiles associated with differential chemotherapy response in serous epithelial ovarian cancer [J].
Bernardini, M ;
Lee, CH ;
Beheshti, B ;
Prasad, M ;
Albert, M ;
Marrano, P ;
Begley, H ;
Shaw, P ;
Covens, A ;
Murphy, J ;
Rosen, B ;
Minkin, S ;
Squire, JA ;
Macgregor, PF .
NEOPLASIA, 2005, 7 (06) :603-613
[5]   Whole genome oligonucleotide-based array comparative genomic hybridization analysis identified fibroblast growth factor I as a prognostic marker for advanced-stage serous ovarian adenocarcinomas [J].
Birrer, Michael J. ;
Johnson, Michael E. ;
Hao, Ke ;
Wong, Kwong-Kwok ;
Park, Dong-Choon ;
Bell, Aaron ;
Welch, William R. ;
Berkowitz, Ross S. ;
Mok, Samuel C. .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (16) :2281-2287
[6]   Bladder cancer stage and outcome by array-based comparative genomic hybridization [J].
Blaveri, E ;
Brewer, JL ;
Roydasgupta, R ;
Fridlyand, J ;
DeVries, S ;
Koppie, T ;
Pejavar, S ;
Mehta, K ;
Carroll, P ;
Simko, JP ;
Waldman, FM .
CLINICAL CANCER RESEARCH, 2005, 11 (19) :7012-7022
[7]   Comprehensive DNA copy number profiling of meningioma using a chromosome 1 tiling path microarray identifies novel candidate tumor suppressor loci [J].
Buckley, PG ;
Jarbo, C ;
Menzel, U ;
Mathiesen, T ;
Scott, C ;
Gregory, SG ;
Langford, CF ;
Dumanski, JP .
CANCER RESEARCH, 2005, 65 (07) :2653-2661
[8]   High-resolution genomic profiles define distinct clinico-pathogenetic subgroups of multiple myeloma patients [J].
Carrasco, DR ;
Tonon, G ;
Huang, YS ;
Zhang, YY ;
Sinha, R ;
Bin, F ;
Stewart, JP ;
Zhan, FG ;
Khatry, D ;
Protopopova, M ;
Protopopov, A ;
Sukhdeo, K ;
Hanamura, I ;
Stephens, O ;
Barlogie, B ;
Anderson, KC ;
Chin, L ;
Shaughnessy, JD ;
Brennan, C ;
DePinho, RA .
CANCER CELL, 2006, 9 (04) :313-325
[9]   Array comparative genomic hybridization reveals genomic copy number changes associated with outcome in diffuse large B-cell lymphomas [J].
Chen, WY ;
Houldsworth, J ;
Olshen, AB ;
Nanjangud, G ;
Chaganti, S ;
Venkatraman, ES ;
Halaas, J ;
Teruya-Feldstein, J ;
Zelenetz, AD ;
Chaganti, RSK .
BLOOD, 2006, 107 (06) :2477-2485
[10]   Array CGH technologies and their applications to cancer genomes [J].
Davies, JJ ;
Wilson, IM ;
Lam, WL .
CHROMOSOME RESEARCH, 2005, 13 (03) :237-248