Inducible transgenics. New lessons on events governing the induction and commitment in mammary tumorigenesis

被引:10
作者
Hulit, J [1 ]
Di Vizio, D [1 ]
Pestell, RG [1 ]
机构
[1] Albert Einstein Coll Med, Div Hormone Respons Canc, Albert Einstein Comprehens Canc Ctr, Bronx, NY 10461 USA
关键词
c-Myc; inducible transgenics; mammary oncogenes; Ras;
D O I
10.1186/bcr297
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer arises from multiple genetic events that together contribute to the established, irreversible malignant phenotype. The development of inducible tissue-specific transgenics has allowed a careful dissection of the events required for induction and subsequent maintenance of tumorigenesis. Mammary gland targeted expression of oncogenic Ras or c-Myc is sufficient far the induction of mammary gland tumorigenesis in the rodent, and when overexpressed together the rate of tumor onset is substantially enhanced. In an exciting recent finding, D'Cruz et al discovered tetracycline-regulated c-Myc overexpression in the mammary gland induced invasive mammary tumors that regressed upon withdrawal of c-Myc expression. Almost one-half of the c-Myc-induced tumors harbored K-ras or N-ras gene point mutations, correlating with tumor persistence on withdrawal of c-Myc transgene expression. These findings suggest maintenance of tumorigenesis may involve a second mutation within the Ras pathway.
引用
收藏
页码:209 / 212
页数:4
相关论文
共 27 条
[1]   Essential role for oncogenic Ras in tumour maintenance [J].
Chin, L ;
Tam, A ;
Pomerantz, J ;
Wong, M ;
Holash, J ;
Bardeesy, N ;
Shen, Q ;
O'Hagan, R ;
Pantginis, J ;
Zhou, H ;
Horner, JW ;
Cordon-Cardo, C ;
Yancopoulos, GD ;
DePinho, RA .
NATURE, 1999, 400 (6743) :468-472
[2]   Induction of cell cycle progression and acceleration of apoptosis are two separable functions of c-Myc: Transrepression correlates with acceleration of apoptosis [J].
Conzen, SD ;
Gottlob, K ;
Kandel, ES ;
Khanduri, P ;
Wagner, AJ ;
O'Leary, M ;
Hay, N .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (16) :6008-6018
[3]   c-MYC induces mammary tumorigenesis by means of a preferred pathway involving spontaneous Kras2 mutations [J].
D'Cruz, CM ;
Gunther, EJ ;
Boxer, RB ;
Hartman, JL ;
Sintasath, L ;
Moody, SE ;
Cox, JD ;
Ha, SI ;
Belka, GK ;
Golant, A ;
Cardiff, RD ;
Chodosh, LA .
NATURE MEDICINE, 2001, 7 (02) :235-239
[4]   Human breast cancer cells generated by oncogenic transformation of primary mammary epithelial cells [J].
Elenbaas, B ;
Spirio, L ;
Koerner, F ;
Fleming, MD ;
Zimonjic, DB ;
Donaher, JL ;
Popescu, NC ;
Hahn, WC ;
Weinberg, RA .
GENES & DEVELOPMENT, 2001, 15 (01) :50-65
[5]   A matter of life and cell death [J].
Evan, G ;
Littlewood, T .
SCIENCE, 1998, 281 (5381) :1317-1322
[6]   Reversible tumorigenesis by MYC in hematopoietic lineages [J].
Felsher, DW ;
Bishop, JM .
MOLECULAR CELL, 1999, 4 (02) :199-207
[7]   Transient excess of MYC activity can elicit genomic instability and tumorigenesis [J].
Felsher, DW ;
Bishop, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) :3940-3944
[8]   Creation of human tumour cells with defined genetic elements [J].
Hahn, WC ;
Counter, CM ;
Lundberg, AS ;
Beijersbergen, RL ;
Brooks, MW ;
Weinberg, RA .
NATURE, 1999, 400 (6743) :464-468
[9]   Reversibility of acute B-cell leukaemia induced by BCR-ABL1 [J].
Huettner, CS ;
Zhang, P ;
Van Etten, RA ;
Tenen, DG .
NATURE GENETICS, 2000, 24 (01) :57-60
[10]   Dual regulation of proliferation and apoptosis: c-myc in bitransgenic murine mammary tumor models [J].
Jamerson, MH ;
Johnson, MD ;
Dickson, RB .
ONCOGENE, 2000, 19 (08) :1065-1071