The problem of cancer dormancy - Understanding the basic mechanisms and identifying therapeutic opportunities

被引:50
作者
Aguirre-Ghiso, Julio A.
机构
[1] SUNY Albany, GenNYSis, Rensselaer, NY 12144 USA
[2] SUNY Albany, Dept Biomed Sci, Sch Publ Hlth, Rensselaer, NY 12144 USA
关键词
quiescence; angiogenesis; metastasis; stem cells; signal transduction;
D O I
10.4161/cc.5.16.3165
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The hiatus observed in the progression of cancer after diagnosis and treatment in a large proportion of patients has led to the notion that a state of cancer dormancy must exist during tumor progression. However, research on this stage of cancer has been limited due to the lack of appropriate models and clinical correlates. Fortunately, the last decade has seen the development of new cancer dormancy models, whole animal and intravital imaging techniques and the molecular characterization of minimal residual disease. These studies enabled researchers to reveal intriguing mechanisms and molecular determinants that define tumor dormancy. It is imperative to understand the basic mechanisms of dormancy, as this will accelerate the development of new markers of progression and novel therapeutic opportunities to induce dormancy and/or eradicate dormant disease. This issue of Cell Cycle includes a "Spotlight on Cancer Dormancy" highlighting major contributions to the field of cancer dormancy from basic and clinical studies. We anticipate that this will initiate a forum of discussion on the problem of cancer dormancy and stimulate investigators to study this rather unexplored but undeniably relevant clinical stage of cancer progression.
引用
收藏
页码:1740 / 1743
页数:4
相关论文
共 51 条
[11]   Role of angiogenesis in tumor growth and metastasis [J].
Folkman, J .
SEMINARS IN ONCOLOGY, 2002, 29 (06) :15-18
[12]  
Folkman J, 1991, Princess Takamatsu Symp, V22, P339
[13]   Tumor dormancy induced by downregulation of urokinase receptor in human carcinoma involves integrin and MAPK signaling [J].
Ghiso, JAA ;
Kovalski, K ;
Ossowski, L .
JOURNAL OF CELL BIOLOGY, 1999, 147 (01) :89-103
[14]   The hallmarks of cancer [J].
Hanahan, D ;
Weinberg, RA .
CELL, 2000, 100 (01) :57-70
[15]   INDIVIDUAL DEVELOPMENT AND UPA-RECEPTOR EXPRESSION OF DISSEMINATED TUMOR-CELLS IN BONE-MARROW - A REFERENCE TO EARLY SYSTEMIC-DISEASE IN SOLID CANCER [J].
HEISS, MM ;
ALLGAYER, H ;
GRUETZNER, KU ;
FUNKE, I ;
BABIC, R ;
JAUCH, KW ;
SCHILDBERG, FW .
NATURE MEDICINE, 1995, 1 (10) :1035-1039
[16]  
INDRACCOLO S, 2006, IN PRESS CELL CYCLE
[17]  
KLEIN CA, 2006, IN PRESS CELL CYCLE
[18]   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
[19]  
LAUFS S, 2006, IN PRESS CELL CYCLE
[20]   EGFR is a transducer of the urokinase receptor initiated signal that is required for in vivo growth of a human carcinoma [J].
Liu, D ;
Ghiso, JAA ;
Estrada, Y ;
Ossowski, L .
CANCER CELL, 2002, 1 (05) :445-457