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A Probabilistic Approach to Estimate the Temporal Order of Pathway Mutations Accounting for Intra-Tumor Heterogeneity.
Wang, Menghan; Xie, Yanqi; Liu, Jinpeng; Li, Austin; Chen, Li; Stromberg, Arnold; Arnold, Susanne M; Liu, Chunming; Wang, Chi.
Affiliation
  • Wang M; Department of Statistics, University of Kentucky, Lexington, KY 40536, USA.
  • Xie Y; Department of Molecular & Cellular Biochemistry, University of Kentucky, Lexington, KY 40508, USA.
  • Liu J; Markey Cancer Center, University of Kentucky, Lexington, KY 40536, USA.
  • Li A; Division of Cancer Biostatistics, Department of Internal Medicine, University of Kentucky, Lexington, KY 40536, USA.
  • Chen L; Department of Computer Science, Princeton University, Princeton, NJ 08540, USA.
  • Stromberg A; Markey Cancer Center, University of Kentucky, Lexington, KY 40536, USA.
  • Arnold SM; Division of Cancer Biostatistics, Department of Internal Medicine, University of Kentucky, Lexington, KY 40536, USA.
  • Liu C; Department of Statistics, University of Kentucky, Lexington, KY 40536, USA.
  • Wang C; Markey Cancer Center, University of Kentucky, Lexington, KY 40536, USA.
Cancers (Basel) ; 16(13)2024 Jul 08.
Article in En | MEDLINE | ID: mdl-39001551
ABSTRACT
The development of cancer involves the accumulation of somatic mutations in several essential biological pathways. Delineating the temporal order of pathway mutations during tumorigenesis is crucial for comprehending the biological mechanisms underlying cancer development and identifying potential targets for therapeutic intervention. Several computational and statistical methods have been introduced for estimating the order of somatic mutations based on mutation profile data from a cohort of patients. However, one major issue of current methods is that they do not take into account intra-tumor heterogeneity (ITH), which limits their ability to accurately discern the order of pathway mutations. To address this problem, we propose PATOPAI, a probabilistic approach to estimate the temporal order of mutations at the pathway level by incorporating ITH information as well as pathway and functional annotation information of mutations. PATOPAI uses a maximum likelihood approach to estimate the probability of pathway mutational events occurring in a specific sequence, wherein it focuses on the orders that are consistent with the phylogenetic structure of the tumors. Applications to whole exome sequencing data from The Cancer Genome Atlas (TCGA) illustrate our method's ability to recover the temporal order of pathway mutations in several cancer types.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cancers (Basel) Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Suiza

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cancers (Basel) Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Suiza