NOV (CCN3) regulation in the growth plate and CCN family member expression in cartilage neoplasia

被引:49
作者
Yu, CY
Le, AT
Yeger, H
Perbal, B
Alman, BA
机构
[1] Hosp Sick Children, Program Dev Biol, Toronto, ON M5G 1X8, Canada
[2] Hosp Sick Children, Dept Lab Med & Pathobiol, Toronto, ON M5G 1X8, Canada
[3] Univ Paris 07, Lab Oncol Virale & Mol, UFR Biochim, F-75005 Paris, France
[4] Univ Toronto, Dept Surg, Toronto, ON, Canada
关键词
NOV; CCN; CTGF; CYR61; WISP-1; growth plate; chondrosarcoma; enchondroma; PTHrP;
D O I
10.1002/path.1468
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Growth plate chondrocytes undergo a coordinated differentiation process resulting in terminal differentiation and new bone formation. Enchondromas are pre-malignant, benign cartilaginous lesions that arise from growth plate chondrocytes that fail to undergo terminal differentiation. NOV (nephroblastoma overexpressed) is a member of the CCN family of proteins, which share a common multi-modular organization. While the role of NOV in chondrocyte development and cartilage neoplasia is not known, other CCN family members play a role in chondrocyte differentiation, or are differentially regulated in cartilage neoplasia. In embryonic murine growth plates, NOV was expressed in pre-hypertrophic and early hypertrophic chondrocytes. PTHrP treatment (which inhibits terminal differentiation) decreased NOV expression in murine femurs maintained in organ culture, and decreased the activity of a NOV reporter construct in vitro. Expression of the CCN family members NOV, CTGF, CYR61, and WISP-1 was examined in 15 chondrosarcomas of various grades and in three enchondromas. Expression of all of the family members was lower in the higher-grade tumours. As identification of the grade of cartilage neoplasia can sometimes be difficult using histology alone, the level of expression of CCN family members could be a useful adjunct in the determination of tumour grade. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:609 / 615
页数:7
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