Identification of c-MYC as a target of the APC pathway

被引:4056
作者
He, TC
Sparks, AB
Rago, C
Hermeking, H
Zawel, L
da Costa, LT
Morin, PJ
Vogelstein, B
Kinzler, KW
机构
[1] Johns Hopkins Oncol Ctr, Baltimore, MD 21231 USA
[2] Howard Hughes Med Inst, Baltimore, MD 21231 USA
[3] Johns Hopkins Univ, Sch Med, Program Human Genet, Baltimore, MD 21205 USA
[4] NIA, Baltimore, MD 21224 USA
关键词
D O I
10.1126/science.281.5382.1509
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The adenomatous polyposis coil gene (APC) is a tumor suppressor gene that is inactivated in most colorectal cancers. Mutations of APC cause aberrant accumulation of beta-catenin, which then binds T cell factor-4 (Tcf-4), causing increased transcriptional activation of unknown genes. Here, the c-MYC oncogene is identified as a target gene in this signaling pathway. Expression of c-MYC was shown to be repressed by wild-type APC and activated by beta-catenin, and these effects were mediated through Tcf-4 binding sites in the c-MYC promoter. These results provide a molecular framework for understanding the previously enigmatic overexpression of c-MYC in colorectal cancers.
引用
收藏
页码:1509 / 1512
页数:4
相关论文
共 42 条
[11]   PROGRESSION OF COLORECTAL-CANCER IS ASSOCIATED WITH MULTIPLE TUMOR SUPPRESSOR GENE DEFECTS BUT INHIBITION OF TUMORIGENICITY IS ACCOMPLISHED BY CORRECTION OF ANY SINGLE DEFECT VIA CHROMOSOME TRANSFER [J].
GOYETTE, MC ;
CHO, K ;
FASCHING, CL ;
LEVY, DB ;
KINZLER, KW ;
PARASKEVA, C ;
VOGELSTEIN, B ;
STANBRIDGE, EJ .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (03) :1387-1395
[12]   IDENTIFICATION AND CHARACTERIZATION OF THE FAMILIAL ADENOMATOUS POLYPOSIS-COLI GENE [J].
GRODEN, J ;
THLIVERIS, A ;
SAMOWITZ, W ;
CARLSON, M ;
GELBERT, L ;
ALBERTSEN, H ;
JOSLYN, G ;
STEVENS, J ;
SPIRIO, L ;
ROBERTSON, M ;
SARGEANT, L ;
KRAPCHO, K ;
WOLFF, E ;
BURT, R ;
HUGHES, JP ;
WARRINGTON, J ;
MCPHERSON, J ;
WASMUTH, J ;
LEPASLIER, D ;
ABDERRAHIM, H ;
COHEN, D ;
LEPPERT, M ;
WHITE, R .
CELL, 1991, 66 (03) :589-600
[13]   A simplified system for generating recombinant adenoviruses [J].
He, TC ;
Zhou, SB ;
da Costa, LT ;
Yu, J ;
Kinzler, KW ;
Vogelstein, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (05) :2509-2514
[14]  
IMASEKI H, 1989, CANCER, V64, P704, DOI 10.1002/1097-0142(19890801)64:3<704::AID-CNCR2820640323>3.0.CO
[15]  
2-S
[16]  
JEN J, 1994, CANCER RES, V54, P6353
[17]   A CELL-CYCLE REGULATOR POTENTIALLY INVOLVED IN GENESIS OF MANY TUMOR TYPES [J].
KAMB, A ;
GRUIS, NA ;
WEAVERFELDHAUS, J ;
LIU, QY ;
HARSHMAN, K ;
TAVTIGIAN, SV ;
STOCKERT, E ;
DAY, RS ;
JOHNSON, BE ;
SKOLNICK, MH .
SCIENCE, 1994, 264 (5157) :436-440
[18]   FUNCTION OF THE C-MYC ONCOPROTEIN [J].
KATO, GJ ;
DANG, CV .
FASEB JOURNAL, 1992, 6 (12) :3065-3072
[19]   Constitutive transcriptional activation by a beta-catenin-Tcf complex in APC(-/-) colon carcinoma [J].
Korinek, V ;
Barker, N ;
Morin, PJ ;
vanWichen, D ;
deWeger, R ;
Kinzler, KW ;
Vogelstein, B ;
Clevers, H .
SCIENCE, 1997, 275 (5307) :1784-1787
[20]   Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4 [J].
Korinek, V ;
Barker, N ;
Moerer, P ;
van Donselaar, E ;
Huls, G ;
Peters, PJ ;
Clevers, H .
NATURE GENETICS, 1998, 19 (04) :379-383