Breast cancer as a systemic disease: a view of metastasis

被引:533
作者
Redig, A. J. [1 ]
McAllister, S. S. [1 ,2 ,3 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Hematol,Dept Med, Boston, MA 02115 USA
[2] Harvard Stem Cell Inst, Boston, MA USA
[3] Broad Inst Harvard & MIT, Cambridge, MA USA
关键词
breast cancer; disseminated tumour cells; metastasis; tumour dormancy; tumour microenvironment; systemic instigation; CIRCULATING TUMOR-CELLS; BONE-MARROW; PROGNOSTIC VALUE; ESTROGEN-RECEPTOR; GENE-EXPRESSION; PROGESTERONE-RECEPTOR; MOLECULAR-MECHANISMS; RECURRENCE DYNAMICS; 1ST-LINE TREATMENT; PRIMARY SURGERY;
D O I
10.1111/joim.12084
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Breast cancer is now the most frequently diagnosed cancer and leading cause of cancer death in women worldwide. Strategies targeting the primary tumour have markedly improved, but systemic treatments to prevent metastasis are less effective; metastatic disease remains the underlying cause of death in the majority of patients with breast cancer who succumb to their disease. The long latency period between initial treatment and eventual recurrence in some patients suggests that a tumour may both alter and respond to the host systemic environment to facilitate and sustain disease progression. Results from studies in animal models suggest that specific subtypes of breast cancer may direct metastasis through recruitment and activation of haematopoietic cells. In this review, we focus on data implicating breast cancer as a systemic disease.
引用
收藏
页码:113 / 126
页数:14
相关论文
共 81 条
[1]   Effects of regular aspirin on long-term cancer incidence and metastasis: a systematic comparison of evidence from observational studies versus randomised trials [J].
Algra, Annemijn M. ;
Rothwell, Peter M. .
LANCET ONCOLOGY, 2012, 13 (05) :518-527
[2]   Molecular mechanisms underlying tumor dormancy [J].
Almog, Nava .
CANCER LETTERS, 2010, 294 (02) :139-146
[3]   The granulin gene family: from cancer to dementia [J].
Bateman, Andrew ;
Bennett, Hugh P. J. .
BIOESSAYS, 2009, 31 (11) :1245-1254
[4]   Aspirin and cancer risk: a quantitative review to 2011 [J].
Bosetti, C. ;
Rosato, V. ;
Gallus, S. ;
Cuzick, J. ;
La Vecchia, C. .
ANNALS OF ONCOLOGY, 2012, 23 (06) :1403-1415
[5]   Circulating tumor cells as predictors of response and failure in breast cancer patients treated with preoperative chemotherapy [J].
Boutrus, Rimoun R. ;
Raad, Rita F. Abi ;
Kuter, Irene ;
Ancukiewicz, Marek ;
Roberts, Lisa ;
Solomon, Natalie ;
Ngo, Taylor ;
Borick, Heather ;
Ryan, Paula ;
Moy, Beverly ;
Gadd, Michele ;
Chien, Jo ;
Younger, Jerry ;
Smith, Barbara ;
Taghian, Alphonse G. ;
Harris, Lyndsay .
INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS, 2013, 28 (01) :17-23
[6]   Role of HIF-1α or in hypoxia-mediated apoptosis, cell proliferation and tumour angiogenesis [J].
Carmeliet, P ;
Dor, Y ;
Herbert, JM ;
Fukumura, D ;
Brusselmans, K ;
Dewerchin, M ;
Neeman, M ;
Bono, F ;
Abramovitch, R ;
Maxwell, P ;
Koch, CJ ;
Ratcliffe, P ;
Moons, L ;
Jain, RK ;
Collen, D ;
Keshet, E .
NATURE, 1998, 394 (6692) :485-490
[7]   Putative growth characteristics of micrometastatic breast cancer [J].
Chambers, Ann F. ;
Goss, Paul E. .
BREAST CANCER RESEARCH, 2008, 10 (06)
[8]   Hypoxia-inducible factor-dependent breast cancer-mesenchymal stem cell bidirectional signaling promotes metastasis [J].
Chaturvedi, Pallavi ;
Gilkes, Daniele M. ;
Wong, Carmen Chak Lui ;
Kshitiz ;
Luo, Weibo ;
Zhang, Huafeng ;
Wei, Hong ;
Takano, Naoharu ;
Schito, Luana ;
Levchenko, Andre ;
Semenza, Gregg L. .
JOURNAL OF CLINICAL INVESTIGATION, 2013, 123 (01) :189-205
[9]   Granulin-epithelin precursor overexpression promotes growth and invasion of hepatocellular carcinoma [J].
Cheung, ST ;
Wong, SY ;
Leung, KL ;
Chen, X ;
So, S ;
Ng, IO ;
Fan, ST .
CLINICAL CANCER RESEARCH, 2004, 10 (22) :7629-7636
[10]   The dynamic change of circulating tumour cells in patients with operable breast cancer before and after chemotherapy based on a multimarker QPCR platform [J].
Chong, M-H ;
Zhao, Y. ;
Wang, J. ;
Zha, X-M ;
Liu, X-A ;
Ling, L-J ;
Du, Q. ;
Wang, S. .
BRITISH JOURNAL OF CANCER, 2012, 106 (10) :1605-1610