Cartilage tumours and bone development: molecular pathology and possible therapeutic targets

被引:197
作者
Bovee, Judith V. M. G. [5 ]
Hogendoorn, Pancras C. W. [5 ]
Wunder, Jay S. [1 ,3 ,4 ]
Alman, Benjamin A. [1 ,2 ]
机构
[1] Univ Toronto, Hosp Sick Children, Div Orthopaed Surg, Toronto, ON MSG 1X8, Canada
[2] Univ Toronto, Hosp Sick Children, Program Dev & Stem Cell Biol, Toronto, ON MSG 1X8, Canada
[3] Univ Toronto, Samuel Lunenfeld Res Inst, Toronto, ON MSG 1X5, Canada
[4] Univ Toronto, Mt Sinai Hosp, Toronto, ON MSG 1X5, Canada
[5] Leiden Univ, Dept Pathol, Med Ctr, NL-2300 RC Leiden, Netherlands
关键词
COMPARATIVE GENOMIC HYBRIDIZATION; HEPARAN-SULFATE PROTEOGLYCAN; P-GLYCOPROTEIN EXPRESSION; CENTRAL CHONDROSARCOMA; PERIPHERAL CHONDROSARCOMA; CHONDROCYTE PROLIFERATION; HEDGEHOG PATHWAY; VEGF EXPRESSION; CELL INVASION; APOPTOSIS;
D O I
10.1038/nrc2869
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
As a group, cartilage tumours are the most common primary bone lesions. They range from benign lesions, such as enchondromas and osteochondromas, to malignant chondrosarcoma. The benign lesions result from the deregulation of the hedgehog signalling pathway, which is involved in normal bone development. These lesions can be the precursors of malignant chondrosarcomas, which are notoriously resistant to conventional chemotherapy and radiotherapy. Cytogenetic studies and mouse models are beginning to identify genes and signalling pathways that have roles in tumour progression, such as hedgehog, p53, insulin-like growth factor, cyclin-dependent kinase 4, hypoxia-inducible factor, matrix metalloproteinases, SRC and AKT, suggesting potential new therapeutic approaches.
引用
收藏
页码:481 / 488
页数:8
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