Gene expression profiling of human sarcomas: Insights into sarcoma biology

被引:263
作者
Baird, K
Davis, S
Antonescu, CR
Harper, UL
Walker, RL
Chen, YD
Glatfelter, AA
Duray, PH
Meltzer, PS
机构
[1] NHGRI, Canc Genet Branch, Bethesda, MD 20892 USA
[2] NCI, Pathol Lab, NIH, Bethesda, MD 20892 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
关键词
D O I
10.1158/0008-5472.CAN-05-1699
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sarcomas are a biologically complex group of tumors of mesenchymal origin. By using gene expression microarray analysis, we aimed to find clues into the cellular differentiation and oncogenic pathways active in these tumors as well as potential biomarkers and therapeutic targets. We examined 181 tumors representing 16 classes of human bone and soft tissue sarcomas on a 12,601-feature cDNA microarray. Remarkably, 2,766 probes differentially expressed across this sample set clearly delineated the various tumor classes. Several genes of potential biological and therapeutic interest were associated with each sarcoma type, including specific tyrosine kinases, transcription factors, and homeobox genes. We also identified subgroups of tumors within the liposarcomas, leiomyosarcomas, and malignant fibrous histiocytomas. We found significant gene ontology correlates for each tumor group and identified similarity to normal tissues by Gene Set Enrichment Analysis. Mutation analysis done on 275 tumor samples revealed that the high expression of epidermal growth factor receptor (EGFR) in certain tumors was not associated with gene mutations. Finally, to further the investigation of human sarcoma biology, we have created an online, publicly available, searchable database housing the data from the gene expression profiles of these tumors (http://watson.nhgri.nih.gov/sarcoma), allowing the user to interactively explore this data set in depth.
引用
收藏
页码:9226 / 9235
页数:10
相关论文
共 56 条
  • [1] Allander SV, 2001, CANCER RES, V61, P8624
  • [2] Primary leiomyosarcoma of bone: A clinicopathologic, immunohistochemical, and ultrastructural study of 33 patients and a literature review
    Antonescu, CR
    Erlandson, RA
    Huvos, AG
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1997, 21 (11) : 1281 - 1294
  • [3] Activin regulation of the follicle-stimulating hormone β-subunit gene involves Smads and the TALE homeodomain proteins Pbx1 and Prep1
    Bailey, JS
    Rave-Harel, N
    McGillivray, SM
    Coss, D
    Mellon, PL
    [J]. MOLECULAR ENDOCRINOLOGY, 2004, 18 (05) : 1158 - 1170
  • [4] Borden EC, 2003, CLIN CANCER RES, V9, P1941
  • [5] The Runx genes:: lineage-specific oncogenes and tumor suppressors
    Cameron, ER
    Neil, JC
    [J]. ONCOGENE, 2004, 23 (24) : 4308 - 4314
  • [6] Coordinated regulation of HOX gene expression in myometrium and uterine leiomyoma
    Cermik, D
    Arici, A
    Taylor, HS
    [J]. FERTILITY AND STERILITY, 2002, 78 (05) : 979 - 984
  • [7] Changing views of the role of matrix metalloproteinases in metastasis
    Chambers, AF
    Matrisian, LM
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (17) : 1260 - 1270
  • [8] Chen Y, 1997, J Biomed Opt, V2, P364, DOI 10.1117/12.281504
  • [9] Genomic analysis of metastasis reveals an essential role for RhoC
    Clark, EA
    Golub, TR
    Lander, ES
    Hynes, RO
    [J]. NATURE, 2000, 406 (6795) : 532 - 535
  • [10] Inflammatory malignant fibrous histiocytomas and dedifferentiated liposarcomas:: histological review, genomic profile, and MDM2 and CDK4 status favour a single entity
    Coindre, JM
    Hostein, I
    Maire, G
    Derré, J
    Guillou, L
    Leroux, A
    Ghnassia, JP
    Collin, F
    Pedeutour, F
    Aurias, A
    [J]. JOURNAL OF PATHOLOGY, 2004, 203 (03) : 822 - 830