Evidence map›Paper›PMID 31791231›Full record

ArticleBMC bioinformatics2019

A probabilistic method for leveraging functional annotations to enhance estimation of the temporal order of pathway mutations during carcinogenesis.

Menghan Wang, Tianxin Yu, Jinpeng Liu, Li Chen, Arnold J Stromberg, John L Villano, Susanne M Arnold, Chunming Liu, Chi Wang

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
–field-weighted citation impact, top 85% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Menghan WangDepartment of Statistics, University of Kentucky, Lexington, USA.
Tianxin YuDepartment of Molecular & Cellular Biology, Roswell Park Comprehensive Cancer Center, Buffalo, USA.
Jinpeng LiuMarkey Cancer Center, University of Kentucky, Lexington, USA.
Li ChenMarkey Cancer Center, University of Kentucky, Lexington, USA.
Arnold J StrombergDepartment of Statistics, University of Kentucky, Lexington, USA.
John L VillanoMarkey Cancer Center, University of Kentucky, Lexington, USA.
Susanne M ArnoldMarkey Cancer Center, University of Kentucky, Lexington, USA.
Chunming LiuMarkey Cancer Center, University of Kentucky, Lexington, USA.
Chi WangMarkey Cancer Center, University of Kentucky, Lexington, USA. chi.wang@uky.edu.ORCID http://orcid.org/0000-0001-8984-4995
University of Kentucky · USRoswell Park Comprehensive Cancer Center · US

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI KATHLEEN L. O'CONNOR · 2013 to 2026
$38.3M
NCI NIH HHS P30 CA177558
6 · The paper itself

Abstract

backgroundCancer arises through accumulation of somatically acquired genetic mutations. An important question is to delineate the temporal order of somatic mutations during carcinogenesis, which contributes to better understanding of cancer biology and facilitates identification of new therapeutic targets. Although a number of statistical and computational methods have been proposed to estimate the temporal order of mutations, they do not account for the differences in the functional impacts of mutations and thus are likely to be obscured by the presence of passenger mutations that do not contribute to cancer progression. In addition, many methods infer the order of mutations at the gene level, which have limited power due to the low mutation rate in most genes.

resultsIn this paper, we develop a Probabilistic Approach for estimating the Temporal Order of Pathway mutations by leveraging functional Annotations of mutations (PATOPA). PATOPA infers the order of mutations at the pathway level, wherein it uses a probabilistic method to characterize the likelihood of mutational events from different pathways occurring in a certain order. The functional impact of each mutation is incorporated to weigh more on a mutation that is more integral to tumor development. A maximum likelihood method is used to estimate parameters and infer the probability of one pathway being mutated prior to another. Simulation studies and analysis of whole exome sequencing data from The Cancer Genome Atlas (TCGA) demonstrate that PATOPA is able to accurately estimate the temporal order of pathway mutations and provides new biological insights on carcinogenesis of colorectal and lung cancers.

conclusionsPATOPA provides a useful tool to estimate temporal order of mutations at the pathway level while leveraging functional annotations of mutations.

Indexed as

Molecular Sequence AnnotationProbabilityCarcinogenesisComputer SimulationDatabases, GeneticHumansMutationMutation RateNeoplasmsReproducibility of ResultsSignal TransductionTime FactorsCarcinogenesisFunctional annotationsPathway analysisSomatic mutations

Identifiers

PMID31791231
PMCPMC6889196
OpenAlexW2993326835

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.