The expression of ccn3(nov) gene in musculoskeletal tumors

被引:95
作者
Manara, MC
Perbal, B
Benini, S
Strammiello, R
Cerisano, V
Perdichizzi, S
Serra, M
Astolfi, A
Bertoni, F
Alami, J
Yeger, H
Picci, P
Scotlandi, K
机构
[1] Ist Orthoped Rizzoli, Lab Ric Oncol, I-40136 Bologna, Italy
[2] Ist Orthoped Rizzoli, Serv Anat Patol, I-40136 Bologna, Italy
[3] Univ Bologna, Dipartimento Patol Sperimentale, Sez Ric Canc, Bologna, Italy
[4] Univ Paris, UFR Biochim, Lab Oncol Virale & Mol, Paris, France
[5] Hosp Sick Children, Dept Paediat Lab Med, Toronto, ON, Canada
关键词
D O I
10.1016/S0002-9440(10)64908-5
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The CCN3(NOV) protein belongs to the CCN [cysteinerich CYR61, connective tissue growth factor (CTGF), nephroblastoma overexpressed gene (Nov)] family of growth regulators, sharing a strikingly conserved multimodular organization but exhibiting distinctive functional features. Although previous studies have revealed an expression of CCN3 protein in several normal tissues, including kidney, nervous system, lung, muscle, and cartilage, less is known about its expression in tumors. In this study, we analyzed the expression of CCN3 in musculoskeletal tumors, using a panel of human cell fines and tissue samples. An association between CCN3 expression and tumor differentiation was observed in rhabdomyosarcoma and cartilage tumors, whereas, in Ewing's sarcoma, the expression of this protein seemed to be associated with a higher risk to develop metastases. CCN3 expression was found in 15 of 45 Ewing's sarcoma tissue samples. In particular, we did not observe any expression of CCN3 in the 15 primary tumors that did not develop metastases. In contrast, 15 of the 30 primary tumors that developed lung and/or bone metachronous metastases showed a high expression of the protein (P < 0.001, Fisher's test). Our studies indicate that CCN3 is generally expressed in the cells of the musculoskeletal system. This protein may play a role both in normal and pathological conditions. However, the regulation of CCN3 expression varies in the different neoplasms and depends on the type of cells. Thus, as reported for other CCN genes, the biological properties and regulation of expression of CCN3 are dependent on the cellular context and the nature of the cells in which it is produced. Further studies will help to clarify the biological role of this protein in musculoskeletal neoplasms.
引用
收藏
页码:849 / 859
页数:11
相关论文
共 35 条
[11]  
DEGIOVANNI C, 1989, ANTICANCER RES, V9, P1943
[12]   GENE FUSION WITH AN ETS DNA-BINDING DOMAIN CAUSED BY CHROMOSOME-TRANSLOCATION IN HUMAN TUMORS [J].
DELATTRE, O ;
ZUCMAN, J ;
PLOUGASTEL, B ;
DESMAZE, C ;
MELOT, T ;
PETER, M ;
KOVAR, H ;
JOUBERT, I ;
DEJONG, P ;
ROULEAU, G ;
AURIAS, A ;
THOMAS, G .
NATURE, 1992, 359 (6391) :162-165
[13]  
Genini M, 1996, INT J CANCER, V66, P571
[14]   EWS-FLI1 and EWS-ERG gene fusions are associated with similar clinical phenotypes in Ewing's sarcoma [J].
Ginsberg, JP ;
de Alava, E ;
Ladanyi, M ;
Wexler, LH ;
Kovar, H ;
Paulussen, M ;
Zoubek, A ;
Dockhorn-Dworniczak, B ;
Juergens, H ;
Wunder, JS ;
Andrulis, IL ;
Malik, R ;
Sorensen, PHB ;
Womer, RB ;
Barr, FG .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (06) :1809-1814
[15]   EWS-ERG AND EWS-FLI1 FUSION TRANSCRIPTS IN EWINGS-SARCOMA AND PRIMITIVE NEUROECTODERMAL TUMORS WITH VARIANT TRANSLOCATIONS [J].
GIOVANNINI, M ;
BIEGEL, JA ;
SERRA, M ;
WANG, JY ;
WEI, YH ;
NYCUM, L ;
EMANUEL, BS ;
EVANS, GA .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (02) :489-496
[16]   Activation-dependent adhesion of human platelets to Cyr61 and Fisp12/mouse connective tissue growth factor is mediated through integrin αIIbβ3 [J].
Jedsadayanmata, A ;
Chen, CC ;
Kireeva, ML ;
Lau, LF ;
Lam, SCT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (34) :24321-24327
[17]   PROVIRAL REARRANGEMENTS AND OVEREXPRESSION OF A NEW CELLULAR GENE (NOV) IN MYELOBLASTOSIS-ASSOCIATED VIRUS TYPE-1-INDUCED NEPHROBLASTOMAS [J].
JOLIOT, V ;
MARTINERIE, C ;
DAMBRINE, G ;
PLASSIART, G ;
BRISAC, M ;
CROCHET, J ;
PERBAL, B .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (01) :10-21
[18]   Adhesion of human umbilical vein endothelial cells to the immediate-early gene product Cyr61 is mediated through integrin αvβ3 [J].
Kireeva, ML ;
Lam, SCT ;
Lau, LF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (05) :3090-3096
[19]   Expression of the human NOV gene in first trimester fetal tissues [J].
Kocialkowski, S ;
Yeger, H ;
Kingdom, J ;
Perbal, B ;
Schofield, PN .
ANATOMY AND EMBRYOLOGY, 2001, 203 (06) :417-427
[20]   The CCN family of angiogenic regulators: The integrin connection [J].
Lau, LF ;
Lam, SCT .
EXPERIMENTAL CELL RESEARCH, 1999, 248 (01) :44-57