| Literature DB >> 29625049 |
Li Ding1, Matthew H Bailey2, Eduard Porta-Pardo3, Vesteinn Thorsson4, Antonio Colaprico5, Denis Bertrand6, David L Gibbs4, Amila Weerasinghe2, Kuan-Lin Huang2, Collin Tokheim7, Isidro Cortés-Ciriano8, Reyka Jayasinghe2, Feng Chen9, Lihua Yu10, Sam Sun11, Catharina Olsen12, Jaegil Kim13, Alison M Taylor14, Andrew D Cherniack14, Rehan Akbani15, Chayaporn Suphavilai6, Niranjan Nagarajan6, Joshua M Stuart16, Gordon B Mills17, Matthew A Wyczalkowski2, Benjamin G Vincent18, Carolyn M Hutter19, Jean Claude Zenklusen20, Katherine A Hoadley21, Michael C Wendl22, Llya Shmulevich4, Alexander J Lazar23, David A Wheeler24, Gad Getz25.
Abstract
The Cancer Genome Atlas (TCGA) has catalyzed systematic characterization of diverse genomic alterations underlying human cancers. At this historic junction marking the completion of genomic characterization of over 11,000 tumors from 33 cancer types, we present our current understanding of the molecular processes governing oncogenesis. We illustrate our insights into cancer through synthesis of the findings of the TCGA PanCancer Atlas project on three facets of oncogenesis: (1) somatic driver mutations, germline pathogenic variants, and their interactions in the tumor; (2) the influence of the tumor genome and epigenome on transcriptome and proteome; and (3) the relationship between tumor and the microenvironment, including implications for drugs targeting driver events and immunotherapies. These results will anchor future characterization of rare and common tumor types, primary and relapsed tumors, and cancers across ancestry groups and will guide the deployment of clinical genomic sequencing.Entities:
Keywords: TCGA; cancer; cancer genomics; omics; oncogenic process
Mesh:
Year: 2018 PMID: 29625049 PMCID: PMC5916814 DOI: 10.1016/j.cell.2018.03.033
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582