Evidence map›Paper›PMID 30201954›Full record

ArticleNature communications2018

Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years.

Jakob Hofvander, Björn Viklund, Anders Isaksson, Otte Brosjö, Fredrik Vult von Steyern, Pehr Rissler, Nils Mandahl, Fredrik Mertens

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Myxoid liposarcoma with nuclear pleomorphism: a clinicopathological and molecular study.Virchows Archiv : an international journal of pathology · 2024
    Article
  10. The diagnostic utility of DNA copy number analysis of core needle biopsies from soft tissue and bone tumors.Laboratory investigation; a journal of technical methods and pathology · 2022
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. The FUS-DDIT3 Interactome in Myxoid Liposarcoma.Neoplasia (New York, N.Y.) · 2019
    Article
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 at 3 institutions in 1 country.

Jakob HofvanderDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, SE-221 84, Lund, Sweden. jakob.hofvander@med.lu.se.ORCID http://orcid.org/0000-0002-8787-1866
Björn ViklundScience for Life Laboratory, Department of Medical Sciences, Uppsala University, SE-751 23, Uppsala, Sweden.
Anders IsakssonScience for Life Laboratory, Department of Medical Sciences, Uppsala University, SE-751 23, Uppsala, Sweden.ORCID http://orcid.org/0000-0001-6576-7825
Otte BrosjöDepartment of Orthopedics, Karolinska Hospital, SE-171 76, Stockholm, Sweden.
Fredrik Vult von SteyernDepartment of Orthopedics, Clinical Sciences, Lund University and Skåne University Hospital, SE-221 85, Lund, Sweden.
Pehr RisslerDepartment of Clinical Genetics and Pathology, University and Regional Laboratories Region Skåne, SE-221 85, Lund, Sweden.
Nils MandahlDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, SE-221 84, Lund, Sweden.
Fredrik MertensDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, SE-221 84, Lund, Sweden.ORCID http://orcid.org/0000-0002-6278-5232
Lund University · SEUppsala University · SEKarolinska University Hospital · SE

Funding

Cancerfonden (Swedish Cancer Society) CAN2017/269
6 · The paper itself

Abstract

To compare clonal evolution in tumors arising through different mechanisms, we selected three types of sarcoma-amplicon-driven well-differentiated liposarcoma (WDLS), gene fusion-driven myxoid liposarcoma (MLS), and sarcomas with complex genomes (CXS)-and assessed the dynamics of chromosome and nucleotide level mutations by cytogenetics, SNP array analysis and whole-exome sequencing. Here we show that the extensive single-cell variation in WDLS has minor impact on clonal key amplicons in chromosome 12. In addition, only a few of the single nucleotide variants in WDLS were present in more than one lesion, suggesting that such mutations are of little significance in tumor development. MLS displays few mutations other than the FUS-DDIT3 fusion, and the primary tumor is genetically sometimes much more complex than its relapses, whereas CXS in general shows a gradual increase of both nucleotide- and chromosome-level mutations, similar to what has been described in carcinomas.

Indexed as

Clonal EvolutionNeoplasm Recurrence, LocalChromosome AberrationsChromosome BandingChromosomesFollow-Up StudiesGene FusionHumansLiposarcomaLiposarcoma, MyxoidMutationNucleotidesOncogene Proteins, FusionPolymorphism, Single NucleotideSarcomaSequence Analysis, DNANucleotidesOncogene Proteins, FusionTranscription Factor CHOP

Identifiers

PMID30201954
PMCPMC6131146
OpenAlexW2891707595

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.