| Literature DB >> 28887051 |
Daniela Senft1, Mark D M Leiserson2, Eytan Ruppin3, Ze'ev A Ronai4.
Abstract
Current efforts in precision oncology largely focus on the benefit of genomics-guided therapy. Yet, advances in sequencing techniques provide an unprecedented view of the complex genetic and nongenetic heterogeneity within individual tumors. Herein, we outline the benefits of integrating genomic and transcriptomic analyses for advanced precision oncology. We summarize relevant computational approaches to detect novel drivers and genetic vulnerabilities, suitable for therapeutic exploration. Clinically relevant platforms to functionally test predicted drugs/drug combinations for individual patients are reviewed. Finally, we highlight the technological advances in single cell analysis of tumor specimens. These may ultimately lead to the development of next-generation cancer drugs, capable of tackling the hurdles imposed by genetic and phenotypic heterogeneity on current anticancer therapies.Entities:
Mesh:
Substances:
Year: 2017 PMID: 28887051 PMCID: PMC5718207 DOI: 10.1016/j.molmed.2017.08.003
Source DB: PubMed Journal: Trends Mol Med ISSN: 1471-4914 Impact factor: 11.951