Id-1 expression and cell survival

被引:130
作者
Wong, YC
Wang, X
Ling, MT
机构
[1] Univ Hong Kong, Fac Med, Dept Anat, Canc Biol Lab, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Fac Med, Inst Mol Technol Drug Discovery & Synth, Cent Lab, Hong Kong, Hong Kong, Peoples R China
关键词
cell proliferation; Id-1; survival; tumour progression;
D O I
10.1023/B:APPT.0000025804.25396.79
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
The Id (inhibitor of differentiation or DNA binding) helix-loop-helix (HLH) proteins are a group of dominant negative regulators of basic HLH transcriptional factors which promote cell differentiation. Recent evidence has revealed that Id proteins, especially Id-1, are also able to promote cell proliferation and cell cycle progression through inactivation of tumour suppressor and activation of growth promoting pathways in mammalian cells. In addition, upregulation of Id-1 has been found in many types of human cancer and its expression levels are also associated with advanced tumour stage. Furthermore, ectopic expression of Id-1 in human cancer cells is able to induce cell proliferation under sub-optimal conditions and protect the cells against apoptosis. These lines of evidence strongly indicate Id-1 as a positive regulator of cell growth and its expression may be a key factor required for tumour cell proliferation. This review will discuss recent evidence on the role of Id-1 in cell proliferation and survival, and its significance in malignant transformation. In addition, we will highlight the recent development in the understanding of the molecular mechanisms responsible for the action of Id-1 in promoting cell survival and tumourigenesis. Finally, the therapeutic implications through inactivation of Id-1 in the treatment of human cancer will also be addressed.
引用
收藏
页码:279 / 289
页数:11
相关论文
共 68 条
[31]   INHIBITION OF AN ERYTHROID-DIFFERENTIATION SWITCH BY THE HELIX-LOOP-HELIX PROTEIN ID1 [J].
LISTER, J ;
FORRESTER, WC ;
BARON, MH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (30) :17939-17946
[32]   Id1 and Id3 are required for neurogenesis, angiogenesis and vascularization of tumour xenografts [J].
Lyden, D ;
Young, AZ ;
Zagzag, D ;
Yan, W ;
Gerald, W ;
O'Reilly, R ;
Bader, BL ;
Hynes, RO ;
Zhuang, Y ;
Manova, K ;
Benezra, R .
NATURE, 1999, 401 (6754) :670-677
[33]   Impaired recruitment of bone-marrow-derived endothelial and hematopoietic precursor cells blocks tumor angiogenesis and growth [J].
Lyden, D ;
Hattori, K ;
Dias, S ;
Costa, C ;
Blaikie, P ;
Butros, L ;
Chadburn, A ;
Heissig, B ;
Marks, W ;
Witte, L ;
Wu, Y ;
Hicklin, D ;
Zhu, ZP ;
Hackett, NR ;
Crystal, RG ;
Moore, MAS ;
Hajjar, KA ;
Manova, K ;
Benezra, R ;
Rafii, S .
NATURE MEDICINE, 2001, 7 (11) :1194-1201
[34]   Microarray analysis uncovers retinoid targets in human bronchial epithelial cells [J].
Ma, Y ;
Koza-Taylor, PH ;
DiMattia, DA ;
Hames, L ;
Fu, HN ;
Dragnev, KH ;
Turi, T ;
Beebe, JS ;
Freemantle, SJ ;
Dmitrovsky, E .
ONCOGENE, 2003, 22 (31) :4924-4932
[35]   Id-1 and Id-2 are overexpressed in pancreatic cancer and in dysplastic lesions in chronic pancreatitis [J].
Maruyama, H ;
Kleeff, J ;
Wildi, S ;
Friess, H ;
Büchler, MW ;
Israel, MA ;
Korc, M .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (03) :815-822
[36]   Inhibitors of cyclin-dependent kinases induce features of replicative senescence in early passage human diploid fibroblasts [J].
McConnell, BB ;
Starborg, M ;
Brookes, S ;
Peters, G .
CURRENT BIOLOGY, 1998, 8 (06) :351-354
[37]  
Nickoloff BJ, 2000, J BIOL CHEM, V275, P27501
[38]   Id proteins are overexpressed in human oral squamous cell carcinomas [J].
Nishimine, M ;
Nakamura, M ;
Mishima, K ;
Kishi, M ;
Kirita, T ;
Sugimura, M ;
Konishi, N .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2003, 32 (06) :350-357
[39]   Id helix-loop-helix proteins in cell growth and differentiation [J].
Norton, JD ;
Deed, RW ;
Craggs, G ;
Sablitzky, F .
TRENDS IN CELL BIOLOGY, 1998, 8 (02) :58-65
[40]   Coupling of cell growth control and apoptosis functions of Id proteins [J].
Norton, JD ;
Atherton, GT .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (04) :2371-2381