A framework for the development of effective anti-metastatic agents

被引:246
作者
Anderson, Robin L. [1 ,2 ,3 ]
Balasas, Theo [4 ]
Callaghan, Juliana [5 ]
Coombes, R. Charles [6 ]
Evans, Jeff [7 ]
Hall, Jacqueline A. [8 ]
Kinrade, Sally [3 ,9 ]
Jones, David [10 ]
Jones, Paul S. [11 ]
Jones, Rob [7 ]
Marshall, John F. [12 ]
Panico, Maria Beatrice [10 ]
Shaw, Jacqui A. [13 ]
Steeg, Patricia S. [14 ]
Sullivan, Mark [3 ,9 ]
Tong, Warwick [3 ]
Westwell, Andrew D. [15 ]
Ritchie, James W. A. [4 ,11 ]
Berg, R.
Drysdale, M.
Eccles, S.
Elvin, P.
Harris, A.
Ireson, C.
Machesky, L.
McLeod, R.
Muschel, R.
Newell, H.
Pittman, M.
Roman, B.
Santos, C.
Sibson, N.
Smith, A.
Waddell, I
机构
[1] Olivia Newton John Canc Res Inst, Translat Breast Canc Program, Heidelberg, Vic, Australia
[2] La Trobe Univ, Sch Canc Med, Bundoora, Vic, Australia
[3] Canc Therapeut Cooperat Res Ctr CTx, Melbourne, Vic, Australia
[4] Canc Res UK CRUK, Commercial Partnerships, London, England
[5] Univ Portsmouth, Res & Innovat Serv, Portsmouth, Hants, England
[6] Hammersmith Hosp, Imperial Coll London, Dept Surg & Canc, London, England
[7] Univ Glasgow, Inst Canc Sci, Glasgow, Lanark, Scotland
[8] Vivacitv Ltd, Res & Dev, Chesham, Bucks, England
[9] Med Dev Global Hlth, Southbank, Vic, Australia
[10] Med & Healthcare Prod Regulatory Agcy, London, England
[11] CRUK, Ctr Drug Dev, London, England
[12] Queen Mary Univ London, Barts Canc Inst, London, England
[13] Univ Leicester, Leicester Canc Res Ctr, Leicester, Leics, England
[14] NCI, Womens Malignancies Branch, Ctr Canc Res, Bethesda, MD 20892 USA
[15] Cardiff Univ, Sch Pharm & Pharmaceut Sci, Cardiff, S Glam, Wales
关键词
BREAST-CANCER METASTASIS; CIRCULATING TUMOR-CELLS; EPITHELIAL-MESENCHYMAL TRANSITION; SURROGATE END-POINTS; BONE-METASTASIS; IN-VIVO; PRECLINICAL MODELS; THERAPEUTIC TARGET; LUNG COLONIZATION; BLADDER-CANCER;
D O I
10.1038/s41571-018-0134-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Most cancer-related deaths are a result of metastasis, and thus the importance of this process as a target of therapy cannot be understated. By asking 'how can we effectively treat cancer?', we do not capture the complexity of a disease encompassing >200 different cancer types - many consisting of multiple subtypes - with considerable intratumoural heterogeneity, which can result in variable responses to a specific therapy. Moreover, we have much less information on the pathophysiological characteristics of metastases than is available for the primary tumour. Most disseminated tumour cells that arrive in distant tissues, surrounded by unfamiliar cells and a foreign microenvironment, are likely to die; however, those that survive can generate metastatic tumours with a markedly different biology from that of the primary tumour. To treat metastasis effectively, we must inhibit fundamental metastatic processes and develop specific preclinical and clinical strategies that do not rely on primary tumour responses. To address this crucial issue, Cancer Research UK and Cancer Therapeutics CRC Australia formed a Metastasis Working Group with representatives from not-for-profit, academic, government, industry and regulatory bodies in order to develop recommendations on how to tackle the challenges associated with treating (micro) metastatic disease. Herein, we describe the challenges identified as well as the proposed approaches for discovering and developing anticancer agents designed specifically to prevent or delay the metastatic outgrowth of cancer.
引用
收藏
页码:185 / 204
页数:20
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