Defining the "Metastasome": Perspectives from the genome and molecular landscape in colorectal cancer for metastasis evolution and clinical consequences

被引:17
作者
Allgayer, Heike [1 ,2 ]
Leupold, Joerg H. [1 ,2 ]
Patil, Nitin [1 ,2 ]
机构
[1] Heidelberg Univ, Med Fac Mannheim, Dept Expt Surg Canc Metastasis, Theodor Kutzer Ufer 1, D-68135 Heidelberg, Germany
[2] Heidelberg Univ, Med Fac Mannheim, Ctr Biomed & Med Technol Mannheim CBTM, Ludolf Krehl Str 6, D-68135 Heidelberg, Germany
关键词
Metastasis; Whole genome; Colorectal cancer; Sequencing; Metastasome; PLASMINOGEN-ACTIVATOR RECEPTOR; MINIMAL RESIDUAL DISEASE; DISSEMINATED TUMOR-CELLS; SRC FAMILY KINASES; UROKINASE-RECEPTOR; LOCALIZATION MICROSCOPY; BONE-MARROW; U-PAR; SUPERRESOLUTION MICROSCOPY; GENE-EXPRESSION;
D O I
10.1016/j.semcancer.2019.07.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastasis still poses the highest challenge for personalized therapy in cancer, partly due to a still incomplete understanding of its molecular evolution. We recently presented the most comprehensive whole-genome study of colorectal metastasis vs. matched primary tumors and suggested novel components of disease progression and metastasis evolution, some of them potentially relevant for targeted therapy. In this review, we try to put these findings into perspective with latest discoveries of colleagues and recent literature, and propose a systematic international team effort to collectively define the "metastasome", a term we introduce to summarize all genomic, epigenomic, transcriptomic, further -omic, molecular and functional characteristics rendering metastases different from primary tumors. Based on recent discoveries, we propose a revised metastasis model for colorectal cancer which is based on a common ancestor clone, early dissemination but flexible early or late stage clonal separation paralleling stromal interactions. Furthermore, we discuss hypotheses on site-specific metastasis, colorectal cancer progression, metastasis-targeted diagnosis and therapy, and metastasis prevention based on latest metastasome data.
引用
收藏
页码:1 / 13
页数:13
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