Evidence map›Paper›PMID 31570656›Full record

ArticleMolecular cancer research : MCR2019

Comparative Genomics Reveals Shared Mutational Landscape in Canine Hemangiosarcoma and Human Angiosarcoma.

Kate Megquier, Jason Turner-Maier, Ross Swofford, Jong-Hyuk Kim, Aaron L Sarver, Chao Wang, Sharadha Sakthikumar, Jeremy Johnson, Michele Koltookian, Mitzi Lewellen and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

65 citing papers in PubMed, 120 citations in OpenAlex.

  1. Review
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  6. FcεRγI promotes canine CD8 chimeric antigen receptor T cell cytotoxicity through a Syk-NF-κB axis.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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5 more citing papers are in PubMed but not listed here.

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

22 authors at 4 institutions in 2 countries.

Kate MegquierBroad Institute of Harvard and MIT, Cambridge, Massachusetts. kmegq@broadinstitute.org kersli@broadinstitute.org.ORCID 0000-0002-1458-0865
Jason Turner-MaierBroad Institute of Harvard and MIT, Cambridge, Massachusetts.
Ross SwoffordBroad Institute of Harvard and MIT, Cambridge, Massachusetts.
Jong-Hyuk KimDepartment of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, Minnesota.ORCID 0000-0002-1645-0036
Aaron L SarverAnimal Cancer Care and Research Program, University of Minnesota, St. Paul, Minnesota.
Chao WangScience for Life Laboratory, Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.
Sharadha SakthikumarBroad Institute of Harvard and MIT, Cambridge, Massachusetts.ORCID 0000-0002-7746-8264
Jeremy JohnsonBroad Institute of Harvard and MIT, Cambridge, Massachusetts.
Michele KoltookianBroad Institute of Harvard and MIT, Cambridge, Massachusetts.
Mitzi LewellenDepartment of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, Minnesota.
Milcah C ScottDepartment of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, Minnesota.
Ashley J SchulteDepartment of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, Minnesota.
Luke BorstDepartment of Clinical Sciences, North Carolina State College of Veterinary Medicine, Raleigh, North Carolina.
Noriko TonomuraBroad Institute of Harvard and MIT, Cambridge, Massachusetts.
Jessica AlfoldiBroad Institute of Harvard and MIT, Cambridge, Massachusetts.
Corrie PainterBroad Institute of Harvard and MIT, Cambridge, Massachusetts.
Rachael ThomasDepartment of Molecular Biomedical Sciences, North Carolina State University College of Veterinary Medicine, and Comparative Medicine Institute, Raleigh, North Carolina.ORCID 0000-0002-3029-8798
Elinor K KarlssonBroad Institute of Harvard and MIT, Cambridge, Massachusetts.ORCID 0000-0002-4343-3776
Matthew Breen *Department of Molecular Biomedical Sciences, North Carolina State University College of Veterinary Medicine, and Comparative Medicine Institute, Raleigh, North Carolina.
Jaime F Modiano *Department of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, Minnesota.ORCID 0000-0001-6398-7648
Ingegerd Elvers *Broad Institute of Harvard and MIT, Cambridge, Massachusetts.
Kerstin Lindblad-Toh *Broad Institute of Harvard and MIT, Cambridge, Massachusetts. kmegq@broadinstitute.org kersli@broadinstitute.org.
Broad Institute · USUniversity of Minnesota · USNorth Carolina State University · USScience for Life Laboratory · SE

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
Transforming family dogs into a powerful and accessible model for human cancerR37CA218570 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KARLSSON, ELINOR · 2018 to 2022
$3.2M
A comprehensive canine genetics resource including gene and variation annotationR24OD018250 · OD · BROAD INSTITUTE, INC. · PI KARLSSON, ELINOR · 2015 to 2017
$1.8M
Bioinformatics approaches to solve the "Missing Driver" problem in solid tumorsR50CA211249 · NCI · UNIVERSITY OF MINNESOTA · PI SARVER, AARON L · 2016 to 2020
$565k
Discovery and Pathogenetic Significance of Chromosome Translocations in AngiosarcomR03CA191713 · NCI · UNIVERSITY OF MINNESOTA · PI MODIANO, JAIME F. · 2016 to 2017
$152k
NCI NIH HHS P30 CA077598NCI NIH HHS R03 CA191713NCI NIH HHS R37 CA218570NCI NIH HHS R50 CA211249NIH HHS R24 OD018250
6 · The paper itself

Abstract

Angiosarcoma is a highly aggressive cancer of blood vessel-forming cells with few effective treatment options and high patient mortality. It is both rare and heterogenous, making large, well-powered genomic studies nearly impossible. Dogs commonly suffer from a similar cancer, called hemangiosarcoma, with breeds like the golden retriever carrying heritable genetic factors that put them at high risk. If the clinical similarity of canine hemangiosarcoma and human angiosarcoma reflects shared genomic etiology, dogs could be a critically needed model for advancing angiosarcoma research. We assessed the genomic landscape of canine hemangiosarcoma via whole-exome sequencing (47 golden retriever hemangiosarcomas) and RNA sequencing (74 hemangiosarcomas from multiple breeds). Somatic coding mutations occurred most frequently in the tumor suppressor

Indexed as

AnimalsBlood VesselsBreastClass Ia Phosphatidylinositol 3-KinaseClass I Phosphatidylinositol 3-KinasesCyclin-Dependent Kinase Inhibitor p15Cyclin-Dependent Kinase Inhibitor p16DogsExome SequencingFemaleGenomeGenomicsHemangiosarcomaHumansMutationTumor Suppressor Protein p53Class Ia Phosphatidylinositol 3-KinaseClass I Phosphatidylinositol 3-KinasesCyclin-Dependent Kinase Inhibitor p15Cyclin-Dependent Kinase Inhibitor p16PIK3CA protein, humanPIK3R1 protein, humanTumor Suppressor Protein p53

Identifiers

PMID31570656
PMCPMC7067513
OpenAlexW2978797341

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.