TRANSFORMATION EFFECTOR AND SUPPRESSOR GENES

被引:10
作者
BOYLAN, MO
ZARBL, H
机构
[1] Division of Toxicology, Whitaker College of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, Massachusetts
关键词
EFFECTOR GENES; SUPPRESSOR GENES; CANCER; ONCOGENES; V-FOS; RHODAMINE; 123; NONTUMORIGENIC REVERTANTS;
D O I
10.1002/jcb.240460303
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
Much has been learned about the molecular basis of cancer from the study of the dominantly acting viral and cellular oncogenes and their normal progenitors, the proto-oncogenes. More recent studies have resulted in the isolation and characterization of several genes prototypic of a second class of cancer genes. Whereas oncogenes act to promote the growth of cells, members of this latter class of genes act to inhibit cellular growth and are believed to contribute to the tumorigenic phenotype only when their activities are absent. This new class of cancer genes is referred to by a number of different names including; anti-oncogenes, recessive oncogenes, growth suppressor genes, tumor suppressor genes and emerogenes. Although only a few of these cancer genes have been identified, to date, it is likely that many additional genes of this class await identification. A third class of genes, necessary for the development of the cancer phenotype, is comprised of the transformation effector genes. These are normal cellular genes that encode proteins that cooperate with or activate oncogene functions and thereby induce the development of the neoplastic phenotype. The inactivation of transformation effector functions would therefore inhibit the ability of certain dominantly acting oncogenes to transform cells. The approaches outlined here describe functional assays for the isolation and molecular characterization of transformation effector and suppressor genes.
引用
收藏
页码:199 / 205
页数:7
相关论文
共 46 条
[11]   A HUMAN DNA SEGMENT WITH PROPERTIES OF THE GENE THAT PREDISPOSES TO RETINOBLASTOMA AND OSTEOSARCOMA [J].
FRIEND, SH ;
BERNARDS, R ;
ROGELJ, S ;
WEINBERG, RA ;
RAPAPORT, JM ;
ALBERT, DM ;
DRYJA, TP .
NATURE, 1986, 323 (6089) :643-646
[12]   STRUCTURAL EVIDENCE FOR THE AUTHENTICITY OF THE HUMAN RETINOBLASTOMA GENE [J].
FUNG, YKT ;
MURPHREE, AL ;
TANG, A ;
QIAN, J ;
HINRICHS, SH ;
BENEDICT, WF .
SCIENCE, 1987, 236 (4809) :1657-1661
[13]   SUPPRESSION OF TUMORIGENICITY WITH CONTINUED EXPRESSION OF THE C-HA-RAS ONCOGENE IN EJ BLADDER CARCINOMA-HUMAN FIBROBLAST HYBRID-CELLS [J].
GEISER, AG ;
DER, CJ ;
MARSHALL, CJ ;
STANBRIDGE, EJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (14) :5209-5213
[14]   HOMOZYGOUS DELETION IN WILMS-TUMORS OF A ZINC-FINGER GENE IDENTIFIED BY CHROMOSOME JUMPING [J].
GESSLER, M ;
POUSTKA, A ;
CAVENEE, W ;
NEVE, RL ;
ORKIN, SH ;
BRUNS, GAP .
NATURE, 1990, 343 (6260) :774-778
[15]   ELEVATED LEVELS OF THE ALPHA-5-BETA-1-FIBRONECTIN RECEPTOR SUPPRESS THE TRANSFORMED PHENOTYPE OF CHINESE HAMSTER OVARY CELLS [J].
GIANCOTTI, FG ;
RUOSLAHTI, E .
CELL, 1990, 60 (05) :849-859
[16]  
HARRIS H, 1969, NATURE, V224, P1314
[17]  
HOEMANN CD, 1990, CELL GROWTH DIFFER, V1, P581
[18]   HOMOLOGIES BETWEEN SIGNAL TRANSDUCING G-PROTEINS AND RAS GENE-PRODUCTS [J].
HURLEY, JB ;
SIMON, MI ;
TEPLOW, DB ;
ROBISHAW, JD ;
GILMAN, AG .
SCIENCE, 1984, 226 (4676) :860-862
[19]   RAT MUTANT-CELLS SHOWING TEMPERATURE SENSITIVITY FOR TRANSFORMATION BY WILD-TYPE MOLONEY MURINE SARCOMA-VIRUS [J].
INOUE, H ;
YUTSUDO, M ;
HAKURA, A .
VIROLOGY, 1983, 125 (01) :242-245
[20]   A RAS-RELATED GENE WITH TRANSFORMATION SUPPRESSOR ACTIVITY [J].
KITAYAMA, H ;
SUGIMOTO, Y ;
MATSUZAKI, T ;
IKAWA, Y ;
NODA, M .
CELL, 1989, 56 (01) :77-84