Role of the β isoform of 14-3-3 proteins in cellular proliferation and oncogenic transformation

被引:81
作者
Takihara, Y
Matsuda, Y
Hara, J
机构
[1] Osaka Univ, Microbial Dis Res Inst, Dept Med Genet & Mol Cell Biol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Sch Med, Dept Dev Med, Suita, Osaka 5650871, Japan
关键词
D O I
10.1093/carcin/21.11.2073
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The 14-3-3 proteins are associated with proto-oncogene and oncogene products. Here, we generated NIH 3T3 cells overexpressing the beta isoform of the 14-3-3 proteins (14-3-3 beta) to examine the function of this isoform in cellular proliferation and oncogenic transformation. Overexpression of 14-3-3 beta in NIH 3T3 cells stimulated cell growth and supported anchorage-independent growth in soft agar medium and tumor formation in nude mice. To elucidate the molecular mechanisms of 14-3-3 beta -mediated NIH 3T3 transformation, we examined the activity of mitogen-activated protein kinase (MAPK) after serum stimulation. Overexpression of 14-3-3 beta augmented MAPK activity after serum stimulation, and MAPK activity correlated well with the amount of 14-3-3 beta expression. The colony-forming ability of NIH 3T3 cells overexpressing 14-3-3 beta in soft agar medium was efficiently abolished by exogenous expression of a dominant-negative mutant of MEK1 and 14-3-3 beta physically interacted with Raf-1 in these cells. These findings indicate that 14-3-3 beta has oncogenic potential, mainly through enhancement of Raf-1 activation and resultant augmentation of signaling in the MAPK cascade.
引用
收藏
页码:2073 / 2077
页数:5
相关论文
共 36 条
[1]   14-3-3 PROTEINS - A HIGHLY CONSERVED, WIDESPREAD FAMILY OF EUKARYOTIC PROTEINS [J].
AITKEN, A ;
COLLINGE, DB ;
VANHEUSDEN, BPH ;
ISOBE, T ;
ROSEBOOM, PH ;
ROSENFELD, G ;
SOLL, J .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (12) :498-501
[2]  
Ausubel FM, 1995, SHORT PROTOCOLS MOL
[3]   INHIBITION OF PHOSPHATIDYLINOSITOL 3-KINASE ACTIVITY BY ASSOCIATION WITH 14-3-3-PROTEINS IN T-CELLS [J].
BONNEFOYBERARD, N ;
LIU, YC ;
VONWILLEBRAND, M ;
SUNG, A ;
ELLY, C ;
MUSTELIN, T ;
YOSHIDA, H ;
ISHIZAKA, K ;
ALTMAN, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (22) :10142-10146
[4]   BCR AND RAF FORM A COMPLEX IN-VIVO VIA 14-3-3-PROTEINS [J].
BRASELMANN, S ;
MCCORMICK, F .
EMBO JOURNAL, 1995, 14 (19) :4839-4848
[5]   14-3-3-PROTEINS ASSOCIATE WITH CDC25-PHOSPHATASES [J].
CONKLIN, DS ;
GALAKTIONOV, K ;
BEACH, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (17) :7892-7896
[6]  
Craparo A, 1997, J BIOL CHEM, V272, P11663
[7]  
DELARCO JE, 1978, P NATL ACAD SCI USA, V75, P4001
[8]   ACTIVATION OF RAF-1 BY 14-3-3-PROTEINS [J].
FANTL, WJ ;
MUSLIN, AJ ;
KIKUCHI, A ;
MARTIN, JA ;
MACNICOL, AM ;
GROSS, RW ;
WILLIAMS, LT .
NATURE, 1994, 371 (6498) :612-614
[9]   Activation of the Raf-1 kinase cascade by coumermycin-induced dimerization [J].
Farrar, MA ;
AlberolaIla, J ;
Perlmutter, RM .
NATURE, 1996, 383 (6596) :178-181
[10]  
FERBY IM, 1994, J BIOL CHEM, V269, P30485