Evidence map›Paper›PMID 28276460›Full record

ArticleScientific reports2017

Genomic Analyses of Breast Cancer Progression Reveal Distinct Routes of Metastasis Emergence.

Anne Bruun Krøigård, Martin Jakob Larsen, Charlotte Brasch-Andersen, Anne-Vibeke Lænkholm, Ann S Knoop, Jeanette Dupont Jensen, Martin Bak, Jan Mollenhauer, Mads Thomassen, Torben A Kruse

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

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  16. Cancer metastasizes to the bone marrow and not to the bone: time for a paradigm shift!European journal of nuclear medicine and molecular imaging · 2018
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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

10 authors at 5 institutions in 1 country.

Anne Bruun KrøigårdDepartment of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Martin Jakob LarsenDepartment of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Charlotte Brasch-AndersenDepartment of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Anne-Vibeke LænkholmDepartment of Pathology, Slagelse Hospital, Slagelse, Denmark.
Ann S KnoopDepartment of Oncology, Rigshospitalet, Copenhagen, Denmark.
Jeanette Dupont JensenDepartment of Oncology, Odense University Hospital, Odense, Denmark.
Martin BakDepartment of Pathology, Odense University Hospital, Odense, Denmark.
Jan MollenhauerLundbeckfonden Center of Excellence NanoCAN, Odense, Denmark.
Mads ThomassenDepartment of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Torben A KruseDepartment of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Odense University Hospital · DKUniversity of Southern Denmark · DKLundbeck Foundation · DKRigshospitalet · DKSlagelse Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A main controversy in cancer research is whether metastatic abilities are present in the most advanced clone of the primary tumor or result from independently acquired aberrations in early disseminated cancer cells as suggested by the linear and the parallel progression models, respectively. The genetic concordance between different steps of malignant progression is mostly unexplored as very few studies have included cancer samples separated by both space and time. We applied whole exome sequencing and targeted deep sequencing to 26 successive samples from six patients with metastatic estrogen receptor (ER)-positive breast cancer. Our data provide support for both linear and parallel progression towards metastasis. We report for the first time evidence of metastasis-to-metastasis seeding in breast cancer. Our results point to three distinct routes of metastasis emergence. This may have profound clinical implications and provides substantial novel molecular insights into the timing and mutational evolution of breast cancer metastasis.

Indexed as

MutationAgedAged, 80 and overBone NeoplasmsBreast NeoplasmsCytoskeletal ProteinsDisease ProgressionExome SequencingFemaleGenomicsHumansLIM Domain ProteinsLiver NeoplasmsMiddle AgedRepressor ProteinsBCL6B protein, humanCytoskeletal ProteinsLIM Domain ProteinsRepressor ProteinsZNF185 protein, human

Identifiers

PMID28276460
PMCPMC5343450
OpenAlexW2594225120

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.