In Vitro Analysis of Integrated Global High-Resolution DNA Methylation Profiling with Genomic Imbalance and Gene Expression in Osteosarcoma

被引:58
作者
Sadikovic, Bekim [1 ,2 ,3 ]
Yoshimoto, Maisa [3 ]
Al-Romaih, Khaldoun [3 ]
Maire, Georges [3 ]
Zielenska, Maria [1 ,2 ]
Squire, Jeremy A. [3 ,4 ]
机构
[1] Hosp Sick Children, Dept Pediat Lab Med, Toronto, ON M5G 1X8, Canada
[2] Hosp Sick Children, Genet & Genome Biol Program, Toronto, ON, Canada
[3] UHN, OCI, Dept Res, Div Cellular & Mol Biol, Toronto, ON, Canada
[4] Queens Univ, Richardson Labs, Dept Pathol & Mol Med, Kingston, ON, Canada
来源
PLOS ONE | 2008年 / 3卷 / 07期
关键词
D O I
10.1371/journal.pone.0002834
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Genetic and epigenetic changes contribute to deregulation of gene expression and development of human cancer. Changes in DNA methylation are key epigenetic factors regulating gene expression and genomic stability. Recent progress in microarray technologies resulted in developments of high resolution platforms for profiling of genetic, epigenetic and gene expression changes. OS is a pediatric bone tumor with characteristically high level of numerical and structural chromosomal changes. Furthermore, little is known about DNA methylation changes in OS. Our objective was to develop an integrative approach for analysis of high-resolution epigenomic, genomic, and gene expression profiles in order to identify functional epi/genomic differences between OS cell lines and normal human osteoblasts. A combination of Affymetrix Promoter Tilling Arrays for DNA methylation, Agilent array-CGH platform for genomic imbalance and Affymetrix Gene 1.0 platform for gene expression analysis was used. As a result, an integrative high-resolution approach for interrogation of genome-wide tumour-specific changes in DNA methylation was developed. This approach was used to provide the first genomic DNA methylation maps, and to identify and validate genes with aberrant DNA methylation in OS cell lines. This first integrative analysis of global cancer-related changes in DNA methylation, genomic imbalance, and gene expression has provided comprehensive evidence of the cumulative roles of epigenetic and genetic mechanisms in deregulation of gene expression networks.
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页数:16
相关论文
共 59 条
[1]   Modulation by decitabine of gene expression and growth of osteosarcoma U2OS cells in vitro and in xenografts: Identification of apoptotic genes as targets for demethylation [J].
Al-Romaih, Khaldoun ;
Somers, Gino R. ;
Bayani, Jane ;
Hughes, Simon ;
Prasad, Mona ;
Cutz, Jean-Claude ;
Xue, Hui ;
Zielenska, Maria ;
Wang, Yuzhuo ;
Squire, Jeremy A. .
CANCER CELL INTERNATIONAL, 2007, 7 (1)
[2]   Decitabine-induced demethylation of 5′ CpG island in GADD45A leads to apoptosis in osteosarcoma cells [J].
Al-Romaih, Khaldoun ;
Sadikovic, Bekim ;
Yoshimoto, Maisa ;
Wang, Yuzhuo ;
Zielenska, Maria ;
Squire, Jeremy A. .
NEOPLASIA, 2008, 10 (05) :471-480
[3]   Differential methylation of human LINE-1 retrotransposons in malignant cells [J].
Alves, G ;
Tatro, A ;
Fanning, T .
GENE, 1996, 176 (1-2) :39-44
[4]   Evaluation of paediatric osteosarcomas by classic cytogenetic and CGH analyses [J].
Batanian, JR ;
Cavalli, LR ;
Aldosari, NM ;
Ma, E ;
Sotelo-Avila, C ;
Ramos, MB ;
Rone, JD ;
Thorpe, CM ;
Haddad, BR .
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 2002, 55 (06) :389-393
[5]   Molecular cytogenetic analysis of medulloblastomas and supratentorial primitive neuroectodermal tumors by using conventional banding, comparative genomic hybridization, and spectral karyotyping [J].
Bayani, J ;
Zielenska, M ;
Marrano, P ;
Ng, YK ;
Taylor, MD ;
Jay, V ;
Rutka, JT ;
Squire, JA .
JOURNAL OF NEUROSURGERY, 2000, 93 (03) :437-448
[6]   Spectral karyotyping identifies recurrent complex rearrangements of chromosomes 8, 17, and 20 in osteosarcomas [J].
Bayani, J ;
Zielenska, M ;
Pandita, A ;
Al-Romaih, K ;
Karaskova, J ;
Harrison, K ;
Bridge, JA ;
Sorensen, P ;
Thorner, P ;
Squire, JA .
GENES CHROMOSOMES & CANCER, 2003, 36 (01) :7-16
[7]  
BEDFORD MT, 1987, CANCER RES, V47, P5274
[8]   A bivalent chromatin structure marks key developmental genes in embryonic stem cells [J].
Bernstein, BE ;
Mikkelsen, TS ;
Xie, XH ;
Kamal, M ;
Huebert, DJ ;
Cuff, J ;
Fry, B ;
Meissner, A ;
Wernig, M ;
Plath, K ;
Jaenisch, R ;
Wagschal, A ;
Feil, R ;
Schreiber, SL ;
Lander, ES .
CELL, 2006, 125 (02) :315-326
[9]   DNA methylation and cancer [J].
Das, PM ;
Singal, R .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (22) :4632-4642
[10]   Functional analysis of CpG methylation in the BRCA1 promoter region [J].
DiNardo, DNM ;
Butcher, DT ;
Robinson, DP ;
Archer, TK ;
Rodenhiser, DI .
ONCOGENE, 2001, 20 (38) :5331-5340