Evidence map›Paper›PMID 31722230›Full record

ReviewSeminars in cancer biology2020

Proteomic research in sarcomas - current status and future opportunities.

Jessica Burns, Christopher P Wilding, Robin L Jones, Paul H Huang

Abstract readReview
In one paragraph

Review in Seminars in cancer biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Review
  2. Article
  3. Circulating Biomarkers in Sarcoma.Current oncology reports · 2025
    Review
  4. Review
  5. Review
  6. Therapeutic impacts of GNE‑477‑loaded HInternational journal of molecular medicine · 2024
    Article
  7. Article
  8. Article
  9. Translational Aspects of Epithelioid Sarcoma: Current Consensus.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Review
  10. Article
  11. Review
  12. TThe Iowa orthopaedic journal · 2023
    Article
  13. Unveiling the role of osteosarcoma-derived secretome in premetastatic lung remodelling.Journal of experimental & clinical cancer research : CR · 2023
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Regorafenib for the Treatment of Sarcoma.Current treatment options in oncology · 2022
    Review
  20. Review
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

4 authors.

Jessica BurnsDivision of Molecular Pathology, The Institute of Cancer Research, London, SW3 6JB, UK.
Christopher P WildingDivision of Molecular Pathology, The Institute of Cancer Research, London, SW3 6JB, UK.
Robin L JonesDivision of Clinical Studies, The Institute of Cancer Research, London SW3 6JB, UK; Sarcoma Unit, The Royal Marsden NHS Foundation Trust, London, SW3 6JJ, UK.
Paul H HuangDivision of Molecular Pathology, The Institute of Cancer Research, London, SW3 6JB, UK. Electronic address: paul.huang@icr.ac.uk.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Sarcomas are a rare group of mesenchymal cancers comprising over 70 different histological subtypes. For the majority of these diseases, the molecular understanding of the basis of their initiation and progression remains unclear. As such, limited clinical progress in prognosis or therapeutic regimens have been made over the past few decades. Proteomics techniques are being increasingly utilised in the field of sarcoma research. Proteomic research efforts have thus far focused on histological subtype characterisation for the improvement of biological understanding, as well as for the identification of candidate diagnostic, predictive, and prognostic biomarkers for use in clinic. However, the field itself is in its infancy, and none of these proteomic research findings have been translated into the clinic. In this review, we provide a brief overview of the proteomic strategies that have been employed in sarcoma research. We evaluate key proteomic studies concerning several rare and ultra-rare sarcoma subtypes including, gastrointestinal stromal tumours, osteosarcoma, liposarcoma, leiomyosarcoma, malignant rhabdoid tumours, Ewing sarcoma, myxofibrosarcoma, and alveolar soft part sarcoma. Consequently, we illustrate how routine implementation of proteomics within sarcoma research, integration of proteomics with other molecular profiling data, and incorporation of proteomics into clinical trial studies has the potential to propel the biological and clinical understanding of this group of complex rare cancers moving forward.

Indexed as

ProteomeProteomicsAnimalsAntineoplastic AgentsBiomarkersDrug DiscoveryHumansMolecular Targeted TherapySarcomaAntineoplastic AgentsBiomarkersProteomeBiomarkersDrug DiscoveryProteomicsSarcomaTargeted Therapy

Identifiers

PMID31722230
PMCPMC7083238

What OpenQuestion holds

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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.