Evidence map›Paper›PMID 19363497›Full record

ArticleNature medicine2009

Copy number analysis indicates monoclonal origin of lethal metastatic prostate cancer.

Wennuan Liu, Sari Laitinen, Sofia Khan, Mauno Vihinen, Jeanne Kowalski, Guoqiang Yu, Li Chen, Charles M Ewing, Mario A Eisenberger, Michael A Carducci and 8 more

Erratum issuedOpen access · greenAbstract readLetter
In one paragraph

Article in Nature medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 349 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
349citing papers in PubMed, 2 pooled it
17.3field-weighted citation impact, top 1% 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

349 citing papers in PubMed, 2 syntheses or guidelines pooled it, 657 citations in OpenAlex.

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289 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 6 institutions in 2 countries.

Wennuan Liu
Sari Laitinen
Sofia Khan
Mauno Vihinen
Jeanne Kowalski
Guoqiang Yu
Li Chen
Charles M Ewing
Mario A Eisenberger
Michael A Carducci
William G Nelson
Srinivasan Yegnasubramanian
Jun Luo
Yue Wang
Jianfeng Xu
William B Isaacs
Tapio Visakorpi
G Steven Bova
Johns Hopkins University · USJohns Hopkins Medicine · USTampere University · FIVirginia Tech · USWake Forest University · USTampere University Hospital · FI

Funding

Modes of Prostate Ca Progression--role of p53 PathwayR01CA092234 · NCI · JOHNS HOPKINS UNIVERSITY · PI BOVA, GEORGE STEVEN · 2001 to 2005
$1.2M
NCI NIH HHS CA92234NCI NIH HHS R01 CA092234
6 · The paper itself

Abstract

Many studies have shown that primary prostate cancers are multifocal and are composed of multiple genetically distinct cancer cell clones. Whether or not multiclonal primary prostate cancers typically give rise to multiclonal or monoclonal prostate cancer metastases is largely unknown, although studies at single chromosomal loci are consistent with the latter case. Here we show through a high-resolution genome-wide single nucleotide polymorphism and copy number survey that most, if not all, metastatic prostate cancers have monoclonal origins and maintain a unique signature copy number pattern of the parent cancer cell while also accumulating a variable number of separate subclonally sustained changes. We find no relationship between anatomic site of metastasis and genomic copy number change pattern. Taken together with past animal and cytogenetic studies of metastasis and recent single-locus genetic data in prostate and other metastatic cancers, these data indicate that despite common genomic heterogeneity in primary cancers, most metastatic cancers arise from a single precursor cancer cell. This study establishes that genomic archeology of multiple anatomically separate metastatic cancers in individuals can be used to define the salient genomic features of a parent cancer clone of proven lethal metastatic phenotype.

Indexed as

Polymorphism, Single NucleotideAnimalsBlack PeopleChromosome MappingChromosomes, Human, Pair 13Chromosomes, Human, Pair 6Comparative Genomic HybridizationDNA DamageDNA, NeoplasmHumansMaleNeoplasm MetastasisNeoplasm StagingOligonucleotide Array Sequence AnalysisPhenotypeProstatic NeoplasmsDNA, Neoplasm

Identifiers

PMID19363497
PMCPMC2839160
OpenAlexW1987439849

What OpenQuestion holds

Textmetadata
LicenceTDM
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.