Evidence map›Paper›PMID 30053712›Full record

ArticleTranslational oncology2018

A Preliminary Proteomic Investigation of Circulating Exosomes and Discovery of Biomarkers Associated with the Progression of Osteosarcoma in a Clinical Model of Spontaneous Disease.

Jacqueline V Brady, Ryan M Troyer, Stephen A Ramsey, Haley Leeper, Liping Yang, Claudia S Maier, Cheri P Goodall, Carl E Ruby, Hassan A M Albarqi, Oleh Taratula and 1 more

Abstract read
In one paragraph

Article in Translational oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

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  20. Role of extracellular vesicles in osteosarcoma.International journal of medical sciences · 2022
    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

11 authors.

Jacqueline V BradyCarlson College of Veterinary Medicine, Department of Clinical Sciences, Oregon State University, Corvallis, OR, USA.
Ryan M TroyerCarlson College of Veterinary Medicine, Department of Clinical Sciences, Oregon State University, Corvallis, OR, USA.
Stephen A RamseyCarlson College of Veterinary Medicine, Department of Biomedical Sciences, Oregon State University, Corvallis, OR, USA.
Haley LeeperCarlson College of Veterinary Medicine, Department of Clinical Sciences, Oregon State University, Corvallis, OR, USA.
Liping YangCollege of Science, Department of Chemistry, Oregon State University, Corvallis, OR, USA.
Claudia S MaierCollege of Science, Department of Chemistry, Oregon State University, Corvallis, OR, USA.
Cheri P GoodallCarlson College of Veterinary Medicine, Department of Clinical Sciences, Oregon State University, Corvallis, OR, USA.
Carl E RubyCarlson College of Veterinary Medicine, Department of Clinical Sciences, Oregon State University, Corvallis, OR, USA.
Hassan A M AlbarqiCollege of Pharmacy, Oregon State University, Corvallis, OR, USA.
Oleh TaratulaCollege of Pharmacy, Oregon State University, Corvallis, OR, USA.
Shay BrachaCarlson College of Veterinary Medicine, Department of Clinical Sciences, Oregon State University, Corvallis, OR, USA. Electronic address: shay.bracha@oregonstate.edu.

Funding

Orbitrap Elite with ETDS10OD020111 · OD · OREGON STATE UNIVERSITY · PI MAIER, CLAUDIA S · 2015 to 2015
$600k
NIH HHS S10 OD020111
6 · The paper itself

Abstract

Circulating cancer exosomes are microvesicles which originate from malignant cells and other organs influenced by the disease and can be found in blood. The exosomal proteomic cargo can often be traced to the cells from which they originated, reflecting the physiological status of these cells. The similarities between cancer exosomes and the tumor cells they originate from exhibit the potential of these vesicles as an invaluable target for liquid biopsies. Exosomes were isolated from the serum of eight osteosarcoma-bearing dogs, five healthy dogs, and five dogs with traumatic fractures. We also characterized exosomes which were collected longitudinally from patients with osteosarcoma prior and 2 weeks after amputation, and eventually upon detection of lung metastasis. Exosomal proteins fraction were analyzed by label-free mass spectrometry proteomics and were validated with immunoblots of selected proteins. Ten exosomal proteins were found that collectively discriminate serum of osteosarcoma patients from serum healthy or fractured dogs with an accuracy of 85%. Additionally, serum from different disease stages could be distinguished with an accuracy of 77% based on exosomal proteomic composition. The most discriminating protein changes for both sample group comparisons were related to complement regulation, suggesting an immune evasion mechanism in early stages of osteosarcoma as well as in advanced disease.

Identifiers

PMID30053712
PMCPMC6077151

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Registered trials

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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.