Overexpression of DAN causes a growth suppression in p53-deficient SAOS-2 cells

被引:22
作者
Hanaoka, E
Ozaki, T
Nakamura, Y
Moriya, H
Nakagawara, A
Sakiyama, S
机构
[1] Chiba Canc Ctr, Res Inst, Div Biochem, Chuo Ku, Chiba 2608717, Japan
[2] Chiba Univ, Sch Med, Dept Orthoped Surg, Chuoh Ku, Chiba 2608677, Japan
关键词
BMP; DAN; growth suppression; p53; SAOS-2;
D O I
10.1006/bbrc.2000.3758
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It has been shown that the expression of DAN as well as Drm/Gremlin, a member of DAN/Cerberus family, is significantly down-regulated in rodent fibroblasts transformed with various oncogenes and overexpression of DAN results in the phenotypic reversion of the transformed phenotypes. In the present study, we examined the expression levels of DAN, BMP-2, BMP-4 and BMPRs (BMP receptors) in five human cell lines derived from bone and soft tissue tumors. Northern blot analysis revealed that DAN mRNA was detected in OS-KH and RMS-NK cells, but was not detectable in SAOS-2, NOS-1, and ASPS-KY cells. Transient overexpression of DAN in SAOS-2 cells, which lack, functional p53 and pRB, resulted in a remarkable growth suppression without the induction of p21(Waf1). Interestingly, overexpression of DAN was associated with a reduction of alkaline phosphatase activity in SAOS-2 cells. Stable transfection of DAN in SAOS-2 cells caused a significant reduction of numbers of drug-resistant colonies, whereas the truncated form of DAN which lacked a possible signal peptide, completely lost this capability. Our results suggest that the secreted form of DAN exerts its growth-suppressive function in SAGS-a cells in a p53-independent manner. (C) 2000 Academic Press.
引用
收藏
页码:20 / 26
页数:7
相关论文
共 34 条
[1]   HIGH-EFFICIENCY TRANSFORMATION OF MAMMALIAN-CELLS BY PLASMID DNA [J].
CHEN, C ;
OKAYAMA, H .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (08) :2745-2752
[2]  
ENOMOTO H, 1994, ONCOGENE, V9, P2785
[3]  
Guo W, 1999, CLIN ORTHOP RELAT R, P175
[4]  
HIRAKI Y, 1991, J BONE MINER RES, V6, P1373
[5]  
HIRANO Y, 1995, ONCOGENE, V10, P1879
[6]   The Xenopus dorsalizing factor gremlin identifies a novel family of secreted proteins that antagonize BMP activities [J].
Hsu, DR ;
Economides, AN ;
Wang, XR ;
Eimon, PM ;
Harland, RM .
MOLECULAR CELL, 1998, 1 (05) :673-683
[7]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[8]   A STRUCTURAL SUPERFAMILY OF GROWTH-FACTORS CONTAINING A CYSTINE KNOT MOTIF [J].
MCDONALD, NQ ;
HENDRICKSON, WA .
CELL, 1993, 73 (03) :421-424
[9]   MOLECULAR MODELING OF THE NORRIE DISEASE PROTEIN PREDICTS A CYSTINE KNOT GROWTH-FACTOR TERTIARY STRUCTURE [J].
MEITINGER, T ;
MEINDL, A ;
BORK, P ;
ROST, B ;
SANDER, C ;
HAASEMANN, M ;
MURKEN, J .
NATURE GENETICS, 1993, 5 (04) :376-380
[10]   A product of DAN, a novel candidate tumour suppressor gene, is secreted into culture medium and suppresses DNA synthesis [J].
Nakamura, Y ;
Ozaki, T ;
Nakagawara, A ;
Sakiyama, S .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (12) :1986-1990