Evidence map›Paper›PMID 28139641›Full record

ArticleNature communications2017

Reconstructing metastatic seeding patterns of human cancers.

Johannes G Reiter, Alvin P Makohon-Moore, Jeffrey M Gerold, Ivana Bozic, Krishnendu Chatterjee, Christine A Iacobuzio-Donahue, Bert Vogelstein, Martin A Nowak

Abstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
–field-weighted citation impact
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

100 citing papers in PubMed.

  1. Trial
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  3. [Evolution of metastases in non-small-cell lung cancer: preliminary results from the TRACERx-PEACE study].Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2026
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40 more citing papers are in PubMed but not listed here.

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

8 authors.

Johannes G ReiterProgram for Evolutionary Dynamics, Harvard University, Cambridge, Massachusetts 02138, USA.ORCID 0000-0002-0170-7353
Alvin P Makohon-MooreThe David M. Rubenstein Center for Pancreatic Cancer Research, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.
Jeffrey M GeroldProgram for Evolutionary Dynamics, Harvard University, Cambridge, Massachusetts 02138, USA.ORCID 0000-0002-6363-2203
Ivana BozicProgram for Evolutionary Dynamics, Harvard University, Cambridge, Massachusetts 02138, USA.
Krishnendu ChatterjeeIST (Institute of Science and Technology) Austria, Klosterneuburg 3400, Austria.
Christine A Iacobuzio-DonahueThe David M. Rubenstein Center for Pancreatic Cancer Research, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.ORCID 0000-0002-4672-3023
Bert VogelsteinThe Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA.
Martin A NowakProgram for Evolutionary Dynamics, Harvard University, Cambridge, Massachusetts 02138, USA.

Funding

MOLECULAR GENETIC ANALYSIS OF COLORECTAL CANCERR37CA043460 · NCI · JOHNS HOPKINS UNIVERSITY · PI VOGELSTEIN, BERT · 1997 to 2016
$7.4M
(PQB6) Genetics of Subclonal Evolution in Pancreatic CancerR01CA179991 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI IACOBUZIO-DONAHUE, CHRISTINE A · 2013 to 2016
$1.3M
Subclonal Evolution in Metastatic Pancreatic CancerF31CA180682 · NCI · JOHNS HOPKINS UNIVERSITY · PI MAKOHON-MOORE, ALVIN · 2013 to 2014
$74k
NCI NIH HHS F31 CA180682NCI NIH HHS R01 CA179991NCI NIH HHS R37 CA043460
6 · The paper itself

Abstract

Reconstructing the evolutionary history of metastases is critical for understanding their basic biological principles and has profound clinical implications. Genome-wide sequencing data has enabled modern phylogenomic methods to accurately dissect subclones and their phylogenies from noisy and impure bulk tumour samples at unprecedented depth. However, existing methods are not designed to infer metastatic seeding patterns. Here we develop a tool, called Treeomics, to reconstruct the phylogeny of metastases and map subclones to their anatomic locations. Treeomics infers comprehensive seeding patterns for pancreatic, ovarian, and prostate cancers. Moreover, Treeomics correctly disambiguates true seeding patterns from sequencing artifacts; 7% of variants were misclassified by conventional statistical methods. These artifacts can skew phylogenies by creating illusory tumour heterogeneity among distinct samples. In silico benchmarking on simulated tumour phylogenies across a wide range of sample purities (15-95%) and sequencing depths (25-800 × ) demonstrates the accuracy of Treeomics compared with existing methods.

Indexed as

Bayes TheoremBenchmarkingDNA, NeoplasmFemaleGenetic HeterogeneityHigh-Throughput Nucleotide SequencingHumansMaleMutationNeoplasm MetastasisOvarian NeoplasmsPancreatic NeoplasmsPhylogenyProstatic NeoplasmsProteomicsDNA, Neoplasm

Identifiers

PMID28139641
PMCPMC5290319

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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.