Tissue-specific tumorigenesis: context matters

被引:231
作者
Schneider, Guenter [1 ,2 ,3 ]
Schmidt-Supprian, Marc [4 ,5 ,6 ]
Rad, Roland [1 ,2 ,3 ]
Saur, Dieter [6 ,7 ,8 ]
机构
[1] Tech Univ Munich, Klinikum Rechts Isar, Dept Med Gastroenterol & GI Oncol 2, Sch Med, Ismaningerstr 22, D-81675 Munich, Germany
[2] German Canc Res Ctr, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[3] German Canc Consortium DKTK, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[4] Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Dept Med Haematol & Oncol 3, Ismaningerstr 22, D-81675 Munich, Germany
[5] DKFZ, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[6] DKTK, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[7] Tech Univ Munich, Klinikum Rechts Isar, Univ Hosp, Sch Med, Ismaningerstr 22, D-81675 Munich, Germany
[8] DKFZ, Div Translat Canc Res, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
基金
欧洲研究理事会;
关键词
K-RAS ONCOGENE; CELL LUNG-CANCER; PANCREATIC STELLATE CELL; GROWTH-FACTOR RECEPTOR; ABL TYROSINE KINASE; STEM-CELLS; TARGETED THERAPY; CTLA-4; BLOCKADE; OF-ORIGIN; C-MYC;
D O I
10.1038/nrc.2017.5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
How can we treat cancer more effectively? Traditionally, tumours from the same anatomical site are treated as one tumour entity. This concept has been challenged by recent breakthroughs in cancer genomics and translational research that have enabled molecular tumour profiling. The identification and validation of cancer drivers that are shared between different tumour types, spurred the new paradigm to target driver pathways across anatomical sites by off-label drug use, or within so-called basket or umbrella trials which are designed to test whether molecular alterations in one tumour entity can be extrapolated to all others. However, recent clinical and preclinical studies suggest that there are tissue-and cell type-specific differences in tumorigenesis and the organization of oncogenic signalling pathways. In this Opinion article, we focus on the molecular, cellular, systemic and environmental determinants of organ-specific tumorigenesis and the mechanisms of context-specific oncogenic signalling outputs. Investigation, recognition and in-depth biological understanding of these differences will be vital for the design of next-generation clinical trials and the implementation of molecularly guided cancer therapies in the future.
引用
收藏
页码:239 / 253
页数:15
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