| Literature DB >> 34816788 |
Ho-Hsiang Wu1, Xing Hua2, Jianxin Shi3, Nilanjan Chatterjee4,5, Bin Zhu3.
Abstract
Identifying cancer driver genes is essential for understanding the mechanisms of carcinogenesis and designing therapeutic strategies. Although driver genes have been identified for many cancer types, it is still not clear whether the selection pressure of driver genes is homogeneous across cancer subtypes. We propose a statistical framework MutScot to improve the identification of driver genes and to investigate the heterogeneity of driver genes across cancer subtypes. Through simulation studies, we show that MutScot properly controls the type I error in detecting driver genes. In addition, we demonstrate that MutScot can identify subtype heterogeneity of driver genes. Applications to three studies in The Cancer Genome Atlas (TCGA) project showcase that MutScot has a desirable sensitivity for detecting driver genes and that MutScot identifies subtype heterogeneity of driver genes in breast cancer and lung cancer with regards to the status of hormone receptor and to the smoking status, respectively.Entities:
Keywords: Somatic mutations; cancer subtype; driver genes; patient heterogeneity.
Mesh:
Year: 2021 PMID: 34816788 PMCID: PMC9527771 DOI: 10.1177/09622802211055854
Source DB: PubMed Journal: Stat Methods Med Res ISSN: 0962-2802 Impact factor: 2.494