Sp1 and kruppel-like factor family of transcription factors in cell growth regulation and cancer

被引:922
作者
Black, AR
Black, JD
Azizkhan-Clifford, J
机构
[1] Roswell Pk Canc Inst, Dept Pharmacol & Therapeut, Grace Canc Drug Ctr, Buffalo, NY 14263 USA
[2] MCP Hahnemann Med Sch, Dept Biochem, Philadelphia, PA USA
关键词
D O I
10.1002/jcp.1111
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Sp/KLF family contains at least twenty identified members which include Sp1-4 and numerous kruppel-like factors. Members of the family bind with varying affinities to sequences designated as 'Sp1 sites' (e.g., GC-boxes, CACCC-boxes, and basic transcription elements). Family members have different transcriptional properties and can modulate each other's activity by a variety of mechanisms. Since cells can express multiple family members, Sp/KLF factors are likely to make up a transcriptional network through which gene expression can be fine-tuned. 'Sp1 site'-dependent transcription can be growth-regulated, and the activity, expression, and/or post-translational modification of multiple family members is altered with cell growth. Furthermore, Sp/KLF factors are involved in many growth-related signal transduction pathways and their overexpression can have positive or negative effects on proliferation. In addition to growth control, Sp/KLF factors have been implicated in apoptosis and angiogenesis; thus, the family is involved in several aspects of tumorigenesis. Consistent with a role in cancer, Sp/KLF factors interact with oncogenes and tumor suppressors, they can be oncogenic themselves, and altered expression of family members has been detected in tumors. Effects of changes in Sp/KLF factors are context-dependent and can appear contradictory. Since these factors act within a network, this diversity of effects may arise from differences in the expression profile of family members in various cells. Thus, it is likely that the properties of the overall network of Sp/KLF factors play a determining role in regulation of cell growth and tumor progression. J. Cell. Physiol. 188: 143-160, 2001. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:143 / 160
页数:18
相关论文
共 273 条
[1]   Positive- and negative-acting Kruppel-like transcription factors bind a transforming growth factor β control element required for expression of the smooth muscle cell differentiation marker SM22α in vivo [J].
Adam, PJ ;
Regan, CP ;
Hautmann, MB ;
Owens, GK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (48) :37798-37806
[2]   Cyclin D1 associates with the TBP-associated factor TAFII250 to regulate Sp1-mediated transcription [J].
Adnane, J ;
Shao, ZH ;
Robbins, PD .
ONCOGENE, 1999, 18 (01) :239-247
[3]   p21WAF1/CIP1 is upregulated by the geranylgeranyltransferase I inhibitor GGTI-298 through a transforming growth factor β- and Sp1-responsive element:: Involvement of the small GTPase RhoA [J].
Adnane, J ;
Bizouarn, FA ;
Qian, YM ;
Hamilton, AD ;
Sebti, SM .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (12) :6962-6970
[4]   Expression and localization of serum/glucocorticoid-induced kinase in the rat ovary: Relation to follicular growth and differentiation [J].
Alliston, TN ;
Gonzalez-Robayna, IJ ;
Buse, P ;
Firestone, GL ;
Richards, JS .
ENDOCRINOLOGY, 2000, 141 (01) :385-395
[5]   Follicle stimulating hormone-regulated expression of serum/glucocorticoid-inducible kinase in rat ovarian granulosa cells: A functional role for the spl family in promoter activity [J].
Alliston, TN ;
Maiyar, AC ;
Buse, P ;
Firestone, GL ;
Richards, JS .
MOLECULAR ENDOCRINOLOGY, 1997, 11 (13) :1934-1949
[6]  
Alroy I, 1999, MOL CELL BIOL, V19, P1961
[7]   Sp3 is a transcriptional repressor of transforming growth factor-β receptors [J].
Ammanamanchi, S ;
Brattain, MG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (05) :3348-3352
[8]   DNA-DAMAGE AND THE DNA-ACTIVATED PROTEIN-KINASE [J].
ANDERSON, CW .
TRENDS IN BIOCHEMICAL SCIENCES, 1993, 18 (11) :433-437
[9]   High Sp1/Sp3 ratios in epithelial cells during epithelial differentiation and cellular transformation correlate with the activation of the HPV-16 promoter [J].
Apt, D ;
Watts, RM ;
Suske, G ;
Bernard, HU .
VIROLOGY, 1996, 224 (01) :281-291
[10]   Casein kinase II-mediated phosphorylation of the C terminus of spl decreases its DNA binding activity [J].
Armstrong, SA ;
Barry, DA ;
Leggett, RW ;
Mueller, CR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (21) :13489-13495