HSF1, A Versatile Factor in Tumorogenesis

被引:28
作者
Calderwood, S. K. [1 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Radiat Oncol, Boston, MA 02215 USA
关键词
Cancer growth metastasis; heat shock factor; HEAT-SHOCK FACTOR-1; TRANSCRIPTION FACTOR HSF1; CARCINOMA IN-VITRO; P-TEFB KINASE; CANCER-CELLS; PROTEIN-KINASE; PHOSPHORYLATION; ACTIVATION; EXPRESSION; SENESCENCE;
D O I
10.2174/156652412803306675
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
HSF1 is an essential factor in the acute response to proteotoxic stress, in which it causes rapid transcription of heat shock protein (HSP) genes in order to permit survival of cells and restoration of global protein quality. In addition to this property however, HSF1 is chronically activated or overexpressed in a wide range of cancers and is essential for multiple pathways of malignant transformation. Studies in recent years indicate a remarkable pleiotropy in the properties of HSF1 in cancer. HSF1 functions as a transcription factor for HSP genes, reminiscent of its role in the stress response, and the resultant elevation in HSP levels leads to a reduction in programmed cell death and senescence and permits overexpression of mutated oncogenic protein clients required to fuel tumor growth. In addition HSF1 plays a role as a signal modulator, stimulating kinase activity, regulating energy metabolism and permitting the development of polyploidy in cancer cells. HSF1 can also function as an inhibitor of transcription and in cooperation with NuRD family factors can repress genes that oppose metastasis. Inhibitors of HSF1 are undergoing selection and future studies may see the testing of HSF1 as a target in cancer therapy.
引用
收藏
页码:1102 / 1107
页数:6
相关论文
共 64 条
[1]   Effects of the flavonoid drug Quercetin on the response of human prostate tumours to hyperthermia in vitro and in vivo [J].
Asea, A ;
Ara, G ;
Teicher, BA ;
Stevenson, MA ;
Calderwood, SK .
INTERNATIONAL JOURNAL OF HYPERTHERMIA, 2001, 17 (04) :347-356
[2]   p53: Guardian of ploidy [J].
Aylon, Yael ;
Oren, Moshe .
MOLECULAR ONCOLOGY, 2011, 5 (04) :315-323
[3]   Molecular chaperones and protein quality control [J].
Bukau, Bernd ;
Weissman, Jonathan ;
Horwich, Arthur .
CELL, 2006, 125 (03) :443-451
[4]  
Calderwood S K, 2010, Sign Transduct Insights, V2, P13
[5]   Heat shock proteins in cancer: chaperones of tumorigenesis [J].
Calderwood, SK ;
Khaleque, MA ;
Sawyer, DB ;
Ciocca, DR .
TRENDS IN BIOCHEMICAL SCIENCES, 2006, 31 (03) :164-172
[6]   Molecular chaperones in mammary cancer growth and breast tumor therapy [J].
Calderwood, Stuart K. ;
Gong, Jianlin .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2012, 113 (04) :1096-1103
[7]   The Shock of Aging: Molecular Chaperones and the Heat Shock Response in Longevity and Aging - A Mini-Review [J].
Calderwood, Stuart K. ;
Murshid, Ayesha ;
Prince, Thomas .
GERONTOLOGY, 2009, 55 (05) :550-558
[8]   Senescent cells, tumor suppression, and organismal aging: Good citizens, bad neighbors [J].
Campisi, J .
CELL, 2005, 120 (04) :513-522
[9]   Transcriptional activity of heat shock factor 1 at 37 °C is repressed through phosphorylation on two distinct serine residues by glycogen synthase kinase 3α and protein kinases Cα, and Cζ [J].
Chu, BY ;
Zhong, R ;
Soncin, F ;
Stevenson, MA ;
Calderwood, SK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (29) :18640-18646
[10]   Sequential phosphorylation by mitogen-activated protein kinase and glycogen synthase kinase 3 represses transcriptional activation by heat shock factor-1 [J].
Chu, BY ;
Soncin, F ;
Price, BD ;
Stevenson, MA ;
Calderwood, SK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (48) :30847-30857