Evidence map›Paper›PMID 35732905›Full record

ArticleCommunications biology2022

A phylogenetic approach to study the evolution of somatic mutational processes in cancer.

Sayaka Miura, Tracy Vu, Jiyeong Choi, Jeffrey P Townsend, Sajjad Karim, Sudhir Kumar

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Cell-cell fusion in cancer: The next cancer hallmark?The international journal of biochemistry & cell biology · 2024
    Review
  6. Article
  7. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Sayaka Miura *Institute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA, USA.ORCID 0000-0001-9881-2848
Tracy Vu *Institute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA, USA.
Jiyeong ChoiInstitute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA, USA.
Jeffrey P TownsendProgram in Computational Biology and Bioinformatics, Yale University, New Haven, CT, USA.ORCID 0000-0002-9890-3907
Sajjad KarimCenter for Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Saudi Arabia.
Sudhir KumarInstitute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA, USA. s.kumar@temple.edu.ORCID 0000-0002-9918-8212
Temple University · USKing Abdulaziz University · SAYale Cancer Center · US

Funding

Bioinformatics of metastatic migration historiesR01LM013385 · NLM · TEMPLE UNIV OF THE COMMONWEALTH · PI KUMAR, SUDHIR · 2020 to 2023
$1.4M
Cellular Phylogenetics and EvolutionR01LM014005 · NLM · TEMPLE UNIV OF THE COMMONWEALTH · PI MIURA, SAYAKA · 2022 to 2024
$1.0M
Bayesian Evolution-Aware Methods for tumor single cell sequencesR21LM012758 · NLM · TEMPLE UNIV OF THE COMMONWEALTH · PI MIURA, SAYAKA · 2017 to 2018
$392k
NLM NIH HHS R01 LM013385NLM NIH HHS R01 LM014005NLM NIH HHS R21 LM012758U.S. Department of Health & Human Services | National Institutes of Health (NIH) LM012758-02U.S. Department of Health & Human Services | National Institutes of Health (NIH) LM013385-03
6 · The paper itself

Abstract

Cancer cell genomes change continuously due to mutations, and mutational processes change over time in patients, leaving dynamic signatures in the accumulated genomic variation in tumors. Many computational methods detect the relative activities of known mutation signatures. However, these methods may produce erroneous signatures when applied to individual branches in cancer cell phylogenies. Here, we show that the inference of branch-specific mutational signatures can be improved through a joint analysis of the collections of mutations mapped on proximal branches of the cancer cell phylogeny. This approach reduces the false-positive discovery rate of branch-specific signatures and can sometimes detect faint signatures. An analysis of empirical data from 61 lung cancer patients supports trends based on computer-simulated datasets for which the correct signatures are known. In lung cancer somatic variation, we detect a decreasing trend of smoking-related mutational processes over time and an increasing influence of APOBEC mutational processes as the tumor evolution progresses. These analyses also reveal patterns of conservation and divergence of mutational processes in cell lineages within patients.

Indexed as

Genome, HumanLung NeoplasmsHumansMutationPhylogeny

Identifiers

PMID35732905
PMCPMC9217972
OpenAlexW4283274128

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.