Micrometastatic disease and metastatic outgrowth: clinical issues and experimental approaches

被引:22
作者
McGowan, Patricia M. [2 ]
Kirstein, Jennifer M. [2 ]
Chambers, Ann F. [1 ]
机构
[1] London Reg Canc Program, London, ON N6A 4L6, Canada
[2] Univ Western Ontario, Dept Med Biophys, London, ON, Canada
关键词
angiogenesis; autophagy; clinical trials; coagulation; immune-mediated dormancy; magnetic resonance imaging; micrometastatic disease; minimal residual disease; recurrence; tumor dormancy; BREAST-CANCER PATIENTS; DORMANT TUMOR-CELLS; CYTOKERATIN-POSITIVE CELLS; MAMMARY-CARCINOMA CELLS; BONE-MARROW; GENE-EXPRESSION; UROKINASE-RECEPTOR; T-CELLS; PROGNOSTIC-SIGNIFICANCE; ANGIOGENIC BURST;
D O I
10.2217/FON.09.73
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastasis from the primary tumor to distant organs is the principal cause of mortality in patients with cancer, While prognostic factors can predict which patients are likely to have their cancer recur, these are not perfect predictors, and some patient's cancers recur even decades after apparently successful treatment. This phenomenon is referred to as dormancy. Data from experimental studies have revealed two categories of metastatic dormancy: cellular dormancy, with solitary cancer cells in cell-cycle arrest; and micrometastatic dormancy, characterized by a balanced state of proliferation and apoptosis, but with no net increase in size. Development of new models and imaging techniques to track the fate of dormant cancer cells is beginning to shed some light on dormancy. Elucidation of the molecular pathways involved in dormancy will advance clinical understanding and may suggest new avenues for treatment to inhibit the revival of these dormant cells, thereby reducing cancer mortality rates.
引用
收藏
页码:1083 / 1098
页数:16
相关论文
共 146 条
[1]   Green fluorescent protein tagging of extracellular signal-regulated kinase and p38 pathways reveals novel dynamics of pathway activation during primary and metastatic growth [J].
Aguirre-Ghiso, JA ;
Ossowski, L ;
Rosenbaum, SK .
CANCER RESEARCH, 2004, 64 (20) :7336-7345
[2]   Urokinase receptor and fibronectin regulate the ERKMAPK to p38MAPK activity ratios that determine carcinoma cell proliferation or dormancy in vivo [J].
Aguirre-Ghiso, JA ;
Liu, D ;
Mignatti, A ;
Kovalski, K ;
Ossowski, L .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (04) :863-879
[3]  
Aguirre-Ghiso JA, 2003, CANCER RES, V63, P1684
[4]   Models, mechanisms and clinical evidence for cancer dormancy [J].
Aguirre-Ghiso, Julio A. .
NATURE REVIEWS CANCER, 2007, 7 (11) :834-846
[5]  
Allan Alison L, 2006, Breast Dis, V26, P87
[6]   Transcriptional Switch of Dormant Tumors to Fast-Growing Angiogenic Phenotype [J].
Almog, Nava ;
Ma, Lili ;
Raychowdhury, Raktima ;
Schwager, Christian ;
Erber, Ralf ;
Short, Sarah ;
Hlatky, Lynn ;
Vajkoczy, Peter ;
Huber, Peter E. ;
Folkman, Judah ;
Abdollahi, Amir .
CANCER RESEARCH, 2009, 69 (03) :836-844
[7]   Most early disseminated cancer cells detected in bone marrow of breast cancer patients have a putative breast cancer stem cell phenotype [J].
Balic, Marija ;
Lin, Henry ;
Young, Lillian ;
Hawes, Debra ;
Giuliano, Armando ;
McNamara, George ;
Datar, Ram H. ;
Cote, Richard J. .
CLINICAL CANCER RESEARCH, 2006, 12 (19) :5615-5621
[8]   Cytokeratin 19 regulates endoplasmic reticulum stress and inhibits ERp29 expression via p38 MAPK/XBP-1 signaling in breast cancer cells [J].
Bambang, I. Fon ;
Lu, Dan ;
Li, Huiping ;
Chiu, Lily-Lily ;
Lau, Quek Choon ;
Koay, Evelyn ;
Zhang, Daohai .
EXPERIMENTAL CELL RESEARCH, 2009, 315 (11) :1964-1974
[9]   CORRELATION OF VLA-4 INTEGRIN EXPRESSION WITH METASTATIC POTENTIAL IN VARIOUS HUMAN TUMOR-CELL LINES [J].
BAO, L ;
PIGOTT, R ;
MATSUMURA, Y ;
BABAN, D ;
TARIN, D .
DIFFERENTIATION, 1993, 52 (03) :239-246
[10]   Inhibition of metastatic outgrowth from single dormant tumor cells by targeting the cytoskeleton [J].
Barkan, Dalit ;
Kleinman, Hynda ;
Simmons, Justin L. ;
Asmussen, Holly ;
Kamaraju, Anil K. ;
Hoenorhoff, Mark J. ;
Liu, Zi-yao ;
Costes, Sylvain V. ;
Cho, Edward H. ;
Lockett, Stephen ;
Khanna, Chand ;
Chambers, Ann F. ;
Green, Jeffrey E. .
CANCER RESEARCH, 2008, 68 (15) :6241-6250