SIGNAL-TRANSDUCTION THERAPY - A NOVEL-APPROACH TO DISEASE MANAGEMENT

被引:168
作者
LEVITZKI, A [1 ]
机构
[1] SUGEN INC,REDWOOD CITY,CA
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1994年 / 226卷 / 01期
关键词
D O I
10.1111/j.1432-1033.1994.tb20020.x
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
In the past decade it has become apparent that many diseases result from aberrations in signaling pathways. These include proliferative diseases such as cancers, atherosclerosis and psoriasis and inflammatory conditions such as sepsis, rheumatoid arthritis and tissue rejection. These findings refocused the research of the medical community to seek new modalities for disease management which essentially consist of designing drugs which intercept cell signaling. In this review, the emerging success in using tyrosine kinase blockers and other signal interceptors, such as protein kinase C blockers, Ras blockers, Ca2+ signaling inhibitors and estrogen antagonists which inhibit growth of cancer cells in vitro and in vivo will be discussed. These signal interceptors, especially tyrosine-kinase blockers, are also able to block inflammatory responses and the proliferation of vascular smooth muscle cells and psoriatic keratinocytes. The utility of signal interceptors in analyzing signal-transduction pathways is also discussed.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 122 条
[71]   A DERIVATIVE OF STAUROSPORINE (CGP-41-251) SHOWS SELECTIVITY FOR PROTEIN-KINASE C INHIBITION AND INVITRO ANTI-PROLIFERATIVE AS WELL AS INVIVO ANTI-TUMOR ACTIVITY [J].
MEYER, T ;
REGENASS, U ;
FABBRO, D ;
ALTERI, E ;
ROSEL, J ;
MULLER, M ;
CARAVATTI, G ;
MATTER, A .
INTERNATIONAL JOURNAL OF CANCER, 1989, 43 (05) :851-856
[72]   HIGH-AFFINITY VEGF BINDING AND DEVELOPMENTAL EXPRESSION SUGGEST FLK-1 AS A MAJOR REGULATOR OF VASCULOGENESIS AND ANGIOGENESIS [J].
MILLAUER, B ;
WIZIGMANNVOOS, S ;
SCHNURCH, H ;
MARTINEZ, R ;
MOLLER, NPH ;
RISAU, W ;
ULLRICH, A .
CELL, 1993, 72 (06) :835-846
[73]   GLIOBLASTOMA GROWTH INHIBITED IN-VIVO BY A DOMINANT-NEGATIVE FLK-1 MUTANT [J].
MILLAUER, B ;
SHAWVER, LK ;
PLATE, KH ;
RISAU, W ;
ULLRICH, A .
NATURE, 1994, 367 (6463) :576-579
[74]  
MOTZER RJ, 1992, CANCER RES, V52, P5775
[75]   THERAPEUTIC POTENTIAL OF CHIMERIC AND MURINE ANTI-(EPIDERMAL GROWTH-FACTOR RECEPTOR) ANTIBODIES IN A METASTASIS MODEL FOR HUMAN-MELANOMA [J].
NARAMURA, M ;
GILLIES, SD ;
MENDELSOHN, J ;
REISFELD, RA ;
MUELLER, BM .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 1993, 37 (05) :343-349
[76]   PREVENTION OF LIPOPOLYSACCHARIDE-INDUCED LETHAL TOXICITY BY TYROSINE KINASE INHIBITORS [J].
NOVOGRODSKY, A ;
VANICHKIN, A ;
PATYA, M ;
GAZIT, A ;
OSHEROV, N ;
LEVITZKI, A .
SCIENCE, 1994, 264 (5163) :1319-1322
[77]   THE TYROSINE KINASE INHIBITOR TYRPHOSTIN BLOCKS THE CELLULAR ACTIONS OF NERVE GROWTH-FACTOR [J].
OHMICHI, M ;
PANG, L ;
RIBON, V ;
GAZIT, A ;
LEVITZKI, A ;
SALTIEL, AR .
BIOCHEMISTRY, 1993, 32 (17) :4650-4658
[78]   SPHINGOSINE-1-PHOSPHATE AS 2ND MESSENGER IN CELL-PROLIFERATION INDUCED BY PDGF AND FCS MITOGENS [J].
OLIVERA, A ;
SPIEGEL, S .
NATURE, 1993, 365 (6446) :557-560
[79]   ISOLATION OF A NOVEL TYROSINE KINASE INHIBITOR, LAVENDUSTIN-A, FROM STREPTOMYCES-GRISEOLAVENDUS [J].
ONODA, T ;
IINUMA, H ;
SASAKI, Y ;
HAMADA, M ;
ISSHIKI, K ;
NAGANAWA, H ;
TAKEUCHI, T ;
TATSUTA, K ;
UMEZAWA, K .
JOURNAL OF NATURAL PRODUCTS, 1989, 52 (06) :1252-1257
[80]   EPIDERMAL-GROWTH-FACTOR-DEPENDENT ACTIVATION OF THE SRC-FAMILY KINASES [J].
OSHEROV, N ;
LEVITZKI, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 225 (03) :1047-1053