Metastasis: recent discoveries and novel treatment strategies

被引:591
作者
Eccles, Suzanne A.
Welch, Danny R.
机构
[1] Inst Canc Res, Tumour Biol & Metastasis Canc Res UK Ctr Canc The, McElwain Labs, Sutton SM2 5NG, Surrey, England
[2] Univ Alabama Birmingham, Dept Pathol, Ctr Comprehens Canc, Natl Fdn Canc Res Ctr Metastasis Res, Birmingham, AL USA
关键词
D O I
10.1016/S0140-6736(07)60781-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Most cancer deaths are due to the development of metastases, hence the most important improvements in morbidity and mortality will result from prevention (or elimination) of such disseminated disease. Some would argue that treatments directed against metastasis are too late because cells have already escaped from the primary tumour. Such an assertion runs contrary to the significant but (for many common adult cancers) fairly modest improvements in survival following the use of adjuvant radiation and chemotherapy designed to eliminate disseminated cells after surgical removal of the primary tumour. Nonetheless, the debate raises important issues concerning the accurate early identification of clonogenic, metastatic cells, the discovery of novel, tractable targets for therapy, and the monitoring of minimal residual disease. We focus on recent findings regarding intrinsic and extrinsic molecular mechanisms controlling metastasis that determine how, when, and where cancers metastasise, and their implications for patient management in the 21st century.
引用
收藏
页码:1742 / 1757
页数:16
相关论文
共 213 条
[1]  
Abrahamsen B, 2005, CURR OPIN MOL THER, V7, P604
[2]   Targeting lymphangiogenesis to prevent tumour metastasis [J].
Achen, M. G. ;
Mann, G. B. ;
Stacker, S. A. .
BRITISH JOURNAL OF CANCER, 2006, 94 (10) :1355-1360
[3]   Tumor lymphangiogenesis and metastatic spread - New players begin to emerge [J].
Achen, Marc G. ;
Stacker, Steven A. .
INTERNATIONAL JOURNAL OF CANCER, 2006, 119 (08) :1755-1760
[4]   Genetic regulators of large-scale transcriptional signatures in cancer [J].
Adler, AS ;
Lin, MH ;
Horlings, H ;
Nuyten, DSA ;
van de Vijver, MJ ;
Chang, HY .
NATURE GENETICS, 2006, 38 (04) :421-430
[5]   The problem of cancer dormancy - Understanding the basic mechanisms and identifying therapeutic opportunities [J].
Aguirre-Ghiso, Julio A. .
CELL CYCLE, 2006, 5 (16) :1740-1743
[6]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[7]   Molecular characterization of the tumor microenvironment in breast cancer [J].
Allinen, M ;
Beroukhim, R ;
Cai, L ;
Brennan, C ;
Lahti-Domenici, J ;
Huang, HY ;
Porter, D ;
Hu, M ;
Chin, L ;
Richardson, A ;
Schnitt, S ;
Sellers, WR ;
Polyak, K .
CANCER CELL, 2004, 6 (01) :17-32
[8]  
Androutsellis-Theotokis A, 2006, NATURE, V442, P823, DOI 10.1038/nature04940
[9]   Simulating the impact of a molecular 'decision-process' on cellular phenotype and multicellular patterns in brain tumors [J].
Athale, C ;
Mansury, Y ;
Deisboeck, TS .
JOURNAL OF THEORETICAL BIOLOGY, 2005, 233 (04) :469-481
[10]  
Bandyopadhyay A, 2005, CANCER BIOL THER, V4, P168