Gene expression profiling for the investigation of soft tissue sarcoma pathogenesis and the identification of diagnostic, prognostic, and predictive biomarkers

被引:32
作者
Beck, Andrew H. [1 ]
West, Robert B. [1 ,2 ]
van de Rijn, Matt [1 ]
机构
[1] Stanford Univ, Med Ctr, Dept Pathol, Stanford, CA 94305 USA
[2] Palo Alto Vet Affairs Hlth Care Syst, Pathol & Lab Serv, Palo Alto, CA USA
关键词
Gene expression profiling; Microarrays; Genomics; Bioinformatics; Tumor biology; Soft tissue tumors; Sarcomas; Biomarkers; Molecular pathology; Surgical pathology; GASTROINTESTINAL STROMAL TUMORS; SSX FUSION TYPE; MALIGNANT FIBROUS HISTIOCYTOMAS; MESENCHYMAL STEM-CELLS; SYNOVIAL SARCOMA; BREAST-CARCINOMA; MICROARRAY DATA; EWINGS-SARCOMA; DERMATOFIBROSARCOMA PROTUBERANS; ALVEOLAR RHABDOMYOSARCOMAS;
D O I
10.1007/s00428-009-0774-2
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Soft tissue sarcomas are malignant neoplasms derived from mesenchymal tissues. Their pathogenesis is poorly understood and there are few effective treatment options for advanced disease. In the past decade, gene expression profiling has been applied to sarcomas to facilitate understanding of sarcoma pathogenesis and to identify diagnostic, prognostic, and predictive markers. In this paper, we review this body of work and discuss how gene expression profiling has led to advancements in the understanding of sarcoma pathobiology, the identification of clinically useful biomarkers, and the refinement of sarcoma classification schemes. Lastly, we conclude with a discussion of strategies to further optimize the translation of gene expression data into a greater understanding of sarcoma pathogenesis and improved clinical outcomes for sarcoma patients.
引用
收藏
页码:141 / 151
页数:11
相关论文
共 98 条
[1]   Expression profiling of synovial sarcoma by cDNA microarrays - Association of ERBB2, IGFBP2, and ELF3 with epithelial differentiation [J].
Allander, SV ;
Illei, PB ;
Chen, YD ;
Antonescu, CR ;
Bittner, M ;
Ladanyi, M ;
Meltzer, PS .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (05) :1587-1595
[2]   Microarray data analysis: from disarray to consolidation and consensus [J].
Allison, DB ;
Cui, XQ ;
Page, GP ;
Sabripour, M .
NATURE REVIEWS GENETICS, 2006, 7 (01) :55-65
[3]  
[Anonymous], 2008, ENZINGER WEISSS SOFT
[4]   A gene expression signature that distinguishes desmoid tumours from nodular fasciitis [J].
Bacac, M ;
Migliavacca, E ;
Stehle, JC ;
McKee, T ;
Delorenzi, M ;
Coindre, JM ;
Guillou, L ;
Stamenkovic, I .
JOURNAL OF PATHOLOGY, 2006, 208 (04) :543-553
[5]   Gene expression profiling of human sarcomas: Insights into sarcoma biology [J].
Baird, K ;
Davis, S ;
Antonescu, CR ;
Harper, UL ;
Walker, RL ;
Chen, YD ;
Glatfelter, AA ;
Duray, PH ;
Meltzer, PS .
CANCER RESEARCH, 2005, 65 (20) :9226-9235
[6]   The synovial sarcoma SYT-SSX2 oncogene remodels the cytoskeleton through activation of the ephrin pathway [J].
Barco, Roy ;
Hunt, Laura B. ;
Frump, Andrea L. ;
Garcia, Christina B. ;
Benesh, Andrew ;
Caldwell, Robert L. ;
Eid, Josiane E. .
MOLECULAR BIOLOGY OF THE CELL, 2007, 18 (10) :4003-4012
[7]   The fibromatosis signature defines a robust stromal response in breast carcinoma [J].
Beck, Andrew H. ;
Espinosa, Inigo ;
Gilks, C. Blake ;
van de Rijn, Matt ;
West, Robert B. .
LABORATORY INVESTIGATION, 2008, 88 (06) :591-601
[8]   The Macrophage Colony-Stimulating Factor 1 Response Signature in Breast Carcinoma [J].
Beck, Andrew H. ;
Espinosa, Inigo ;
Edris, Badreddin ;
Li, Rui ;
Montgomery, Kelli ;
Zhu, Shirley ;
Varma, Sushama ;
Marinelli, Robert J. ;
van de Rijn, Matt ;
West, Robert B. .
CLINICAL CANCER RESEARCH, 2009, 15 (03) :778-787
[9]   Linking oncogenic pathways with therapeutic opportunities [J].
Bild, Andrea H. ;
Potti, Anil ;
Nevins, Joseph R. .
NATURE REVIEWS CANCER, 2006, 6 (09) :735-U13