TRANSCRIPTION AND CANCER

被引:38
作者
COX, PM
GODING, CR
机构
[1] Transcriptional Control Laboratory, Marie Curie Cancer Research, Surrey, RH8 OTL, The Chart, Oxted
关键词
D O I
10.1038/bjc.1991.151
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The normal growth, development and function of an organism requires precise and co-ordinated control of gene expression. A major part of this control is exerted by regulating messenger RNA (mRNA) production and involves complex interactions between an array of transcriptionally active proteins and specific regulatory DNA sequences. The combination of such proteins and DNA sequences is specific for given gene or group of genes in a particular cell type and the proteins regulating the same gene may vary between cell types. In addition the expression or activity of these regulatory proteins may be modified depending on the state of differentiation of a cell or in response to an external stimulus. Thus,the differentiation of embryonic cells into diverse tissues is achieved and the mature structure and function of the organism is maintained. This review focusses on the role of perturbations of these transcriptional controls in neoplasia. Deregulation of transcription may result in the failure to express genes responsible for cellular differentation, or alternatively, in the transcription of genes involved in cell division, through the inappropriate expression or activation of positivelyacting transcription factors and nuclear oncogenes. Whether the biochemical abnormalities that lead to the disordered growth and differentiation of a malignant tumour affect cell surface receptors, membrane or cytoplasmic signalling proteins or nuclear transcription factors, the end result is the inappropriate expression of some genes and failure to express others. Current research is starting to elucidate which of the elements of this complicated system are important in neoplasia.
引用
收藏
页码:651 / 662
页数:12
相关论文
共 167 条
[131]  
ROBERTS AB, 1985, CANCER SURV, V4, P4
[132]   A GENE ACTIVATED BY GROWTH-FACTORS IS RELATED TO THE ONCOGENE V-JUN [J].
RYDER, K ;
LAU, LF ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (05) :1487-1491
[133]   JUN-D - A 3RD MEMBER OF THE JUN GENE FAMILY [J].
RYDER, K ;
LANAHAN, A ;
PEREZALBUERNE, E ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (05) :1500-1503
[134]   DELINEATION OF 3 FUNCTIONAL DOMAINS OF THE TRANSCRIPTIONAL ACTIVATOR ENCODED BY THE C-MYB PROTOONCOGENE [J].
SAKURA, H ;
CHIE, KI ;
NAGASE, T ;
NAKAGOSHI, H ;
GONDA, TJ ;
ISHII, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (15) :5758-5762
[135]   THE C-ERB-A PROTEIN IS A HIGH-AFFINITY RECEPTOR FOR THYROID-HORMONE [J].
SAP, J ;
MUNOZ, A ;
DAMM, K ;
GOLDBERG, Y ;
GHYSDAEL, J ;
LEUTZ, A ;
BEUG, H ;
VENNSTROM, B .
NATURE, 1986, 324 (6098) :635-640
[136]   FOS-ASSOCIATED CELLULAR P39 IS RELATED TO NUCLEAR TRANSCRIPTION FACTOR-AP-1 [J].
SASSONECORSI, P ;
LAMPH, WW ;
KAMPS, M ;
VERMA, IM .
CELL, 1988, 54 (04) :553-560
[137]   A HUMAN LYMPHOID-SPECIFIC TRANSCRIPTION FACTOR THAT ACTIVATES IMMUNOGLOBULIN GENES IS A HOMOEOBOX PROTEIN [J].
SCHEIDEREIT, C ;
CROMLISH, JA ;
GERSTER, T ;
KAWAKAMI, K ;
BALMACEDA, CG ;
CURRIE, RA ;
ROEDER, RG .
NATURE, 1988, 336 (6199) :551-557
[138]   DNA-BINDING BY PROTEINS [J].
SCHLEIF, R .
SCIENCE, 1988, 241 (4870) :1182-1187
[139]   A CONSERVED FAMILY OF NUCLEAR PROTEINS CONTAINING STRUCTURAL ELEMENTS OF THE FINGER PROTEIN ENCODED BY KRUPPEL, A DROSOPHILA SEGMENTATION GENE [J].
SCHUH, R ;
AICHER, W ;
GAUL, U ;
COTE, S ;
PREISS, A ;
MAIER, D ;
SEIFERT, E ;
NAUBER, U ;
SCHRODER, C ;
KEMLER, R ;
JACKLE, H .
CELL, 1986, 47 (06) :1025-1032
[140]   AMPLIFIED DNA WITH LIMITED HOMOLOGY TO MYC CELLULAR ONCOGENE IS SHARED BY HUMAN NEURO-BLASTOMA CELL-LINES AND A NEURO-BLASTOMA TUMOR [J].
SCHWAB, M ;
ALITALO, K ;
KLEMPNAUER, KH ;
VARMUS, HE ;
BISHOP, JM ;
GILBERT, F ;
BRODEUR, G ;
GOLDSTEIN, M ;
TRENT, J .
NATURE, 1983, 305 (5931) :245-248