TY - JOUR
T1 - Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics
AU - The Cancer Genome Atlas Research Network
AU - Ding, Li
AU - Bailey, Matthew H.
AU - Porta-Pardo, Eduard
AU - Thorsson, Vesteinn
AU - Colaprico, Antonio
AU - Bertrand, Denis
AU - Gibbs, David L.
AU - Weerasinghe, Amila
AU - Huang, Kuan lin
AU - Tokheim, Collin
AU - Cortés-Ciriano, Isidro
AU - Jayasinghe, Reyka
AU - Chen, Feng
AU - Yu, Lihua
AU - Sun, Sam
AU - Olsen, Catharina
AU - Kim, Jaegil
AU - Taylor, Alison M.
AU - Cherniack, Andrew D.
AU - Akbani, Rehan
AU - Suphavilai, Chayaporn
AU - Nagarajan, Niranjan
AU - Stuart, Joshua M.
AU - Mills, Gordon B.
AU - Wyczalkowski, Matthew A.
AU - Vincent, Benjamin G.
AU - Hutter, Carolyn M.
AU - Zenklusen, Jean Claude
AU - Hoadley, Katherine A.
AU - Wendl, Michael C.
AU - Shmulevich, llya
AU - Lazar, Alexander J.
AU - Wheeler, David A.
AU - Getz, Gad
AU - Caesar-Johnson, Samantha J.
AU - Demchok, John A.
AU - Felau, Ina
AU - Kasapi, Melpomeni
AU - Ferguson, Martin L.
AU - Sofia, Heidi J.
AU - Tarnuzzer, Roy
AU - Wang, Zhining
AU - Yang, Liming
AU - Zhang, Jiashan (Julia)
AU - Chudamani, Sudha
AU - Liu, Jia
AU - Lolla, Laxmi
AU - Naresh, Rashi
AU - Pihl, Todd
AU - Baudin, Eric
N1 - Publisher Copyright:
© 2018 The Authors
PY - 2018/4/5
Y1 - 2018/4/5
N2 - 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. A synthesized view on oncogenic processes based on PanCancer Atlas analyses highlights the complex impact of genome alterations on the signaling and multi-omic profiles of human cancers as well as their influence on tumor microenvironment.
AB - 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. A synthesized view on oncogenic processes based on PanCancer Atlas analyses highlights the complex impact of genome alterations on the signaling and multi-omic profiles of human cancers as well as their influence on tumor microenvironment.
KW - TCGA
KW - cancer
KW - cancer genomics
KW - omics
KW - oncogenic process
UR - http://www.scopus.com/inward/record.url?scp=85044744316&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2018.03.033
DO - 10.1016/j.cell.2018.03.033
M3 - Article
C2 - 29625049
AN - SCOPUS:85044744316
SN - 0092-8674
VL - 173
SP - 305-320.e10
JO - Cell
JF - Cell
IS - 2
ER -