Oncogenes come of age

被引:18
作者
Varmus, H. [1 ]
Pao, W. [1 ]
Politi, K. [1 ]
Podsypanina, K. [1 ]
Du, Y. -C. N. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Program Canc Biol & Genet, New York, NY 10021 USA
来源
MOLECULAR APPROACHES TO CONTROLLING CANCER | 2005年 / 70卷
关键词
D O I
10.1101/sqb.2005.70.039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mutations of proto-oncogenes are common events in the pathogenesis of cancers, as shown in a wide range of studies during the 30 years since the discovery of these genes. The benefits of novel therapies that target the products of mutant alleles in human cancers, and the demonstrated dependence of cancers in mouse models on continued expression of initiating oncegenes, are especially promising signs that revolutionary improvements in cancer care are possible. Full realization of the promise of targeted therapies, however, will require better definitions of the genotypes of human cancers, new approaches to interrupt the biochemical consequences of oncogenic mutations, and a greater understanding of drug resistance and tumor progression. In this paper, we summarize recent efforts toward these goals in our laboratory and others.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 61 条
[31]   Irreversible inhibitors of the EGF receptor may circumvent acquired resistance to gefitinib [J].
Kwak, EL ;
Sordella, R ;
Bell, DW ;
Godin-Heymann, N ;
Okimoto, RA ;
Brannigan, BW ;
Harris, PL ;
Driscoll, DR ;
Fidias, P ;
Lynch, TJ ;
Rabindran, SK ;
McGinnis, JP ;
Wissner, A ;
Sharma, SV ;
Isselbacher, KJ ;
Settleman, J ;
Haber, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (21) :7665-7670
[32]   Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib [J].
Lynch, TJ ;
Bell, DW ;
Sordella, R ;
Gurubhagavatula, S ;
Okimoto, RA ;
Brannigan, BW ;
Harris, PL ;
Haserlat, SM ;
Supko, JG ;
Haluska, FG ;
Louis, DN ;
Christiani, DC ;
Settleman, J ;
Haber, DA .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (21) :2129-2139
[33]   The protein kinase complement of the human genome [J].
Manning, G ;
Whyte, DB ;
Martinez, R ;
Hunter, T ;
Sudarsanam, S .
SCIENCE, 2002, 298 (5600) :1912-+
[34]   ROUS SARCOMA VIRUS - A FUNCTION REQUIRED FOR MAINTENANCE OF TRANSFORMED STATE [J].
MARTIN, GS .
NATURE, 1970, 227 (5262) :1021-&
[35]   Conditional activation of Neu in the mammary epithelium of transgenic mice results in reversible pulmonary metastasis [J].
Moody, SE ;
Sarkisian, CJ ;
Hahn, KT ;
Gunther, EJ ;
Pickup, S ;
Dugan, KD ;
Innocent, N ;
Cardiff, RD ;
Schnall, MD ;
Chodosh, LA .
CANCER CELL, 2002, 2 (06) :451-461
[36]   The rise and fall of apoptosis during multistage tumorigenesis: Down-modulation contributes to tumor progression from angiogenic progenitors [J].
Naik, P ;
Karrim, J ;
Hanahan, D .
GENES & DEVELOPMENT, 1996, 10 (17) :2105-2116
[37]  
Naoki K, 2002, CANCER RES, V62, P7001
[38]   EGFR mutations in lung cancer:: Correlation with clinical response to gefitinib therapy [J].
Paez, JG ;
Jänne, PA ;
Lee, JC ;
Tracy, S ;
Greulich, H ;
Gabriel, S ;
Herman, P ;
Kaye, FJ ;
Lindeman, N ;
Boggon, TJ ;
Naoki, K ;
Sasaki, H ;
Fujii, Y ;
Eck, MJ ;
Sellers, WR ;
Johnson, BE ;
Meyerson, M .
SCIENCE, 2004, 304 (5676) :1497-1500
[39]   KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib [J].
Pao, W ;
Wang, TY ;
Riely, GJ ;
Miller, VA ;
Pan, QL ;
Ladanyi, M ;
Zakowski, MF ;
Heelan, RT ;
Kris, MG ;
Varmus, HE .
PLOS MEDICINE, 2005, 2 (01) :57-61
[40]   Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain [J].
Pao, W ;
Miller, VA ;
Politi, KA ;
Riely, GJ ;
Somwar, R ;
Zakowski, MF ;
Kris, MG ;
Varmus, H .
PLOS MEDICINE, 2005, 2 (03) :225-235