AI Article Synopsis

  • Cancer driver gene alterations are crucial in cancer development, involving oncogenes, tumor suppressors, and dual role genes that behave differently depending on context.
  • Moonlight is a new tool that uses various -omics data to identify important cancer driver genes and has analyzed over 8000 tumor samples, finding 3310 oncogenic mediators, including 151 with dual roles.
  • The research reveals insights into tumor heterogeneity and may assist in making informed therapeutic choices by exploring how different tissue types affect gene behavior and confirming critical genes through cell-line datasets.

Article Abstract

Cancer driver gene alterations influence cancer development, occurring in oncogenes, tumor suppressors, and dual role genes. Discovering dual role cancer genes is difficult because of their elusive context-dependent behavior. We define oncogenic mediators as genes controlling biological processes. With them, we classify cancer driver genes, unveiling their roles in cancer mechanisms. To this end, we present Moonlight, a tool that incorporates multiple -omics data to identify critical cancer driver genes. With Moonlight, we analyze 8000+ tumor samples from 18 cancer types, discovering 3310 oncogenic mediators, 151 having dual roles. By incorporating additional data (amplification, mutation, DNA methylation, chromatin accessibility), we reveal 1000+ cancer driver genes, corroborating known molecular mechanisms. Additionally, we confirm critical cancer driver genes by analysing cell-line datasets. We discover inactivation of tumor suppressors in intron regions and that tissue type and subtype indicate dual role status. These findings help explain tumor heterogeneity and could guide therapeutic decisions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941958PMC
http://dx.doi.org/10.1038/s41467-019-13803-0DOI Listing

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