Evidence map›Paper›PMID 32571313›Full record

ArticleBMC veterinary research2020

Chromatin run-on sequencing analysis finds that ECM remodeling plays an important role in canine hemangiosarcoma pathogenesis.

Chinatsu Mukai, Eunju Choi, Kelly L Sams, Elena Zu Klampen, Lynne Anguish, Brooke A Marks, Edward J Rice, Zhong Wang, Lauren A Choate, Shao-Pei Chou and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC veterinary research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Author's reply to the letter to the editor ofJournal of the Korean Association of Oral and Maxillofacial Surgeons · 2024
    Article
  2. Article
  3. Research on Predicting the Occurrence of Hepatocellular Carcinoma Based on Notch Signal-Related Genes Using Machine Learning Algorithms.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Article
  4. Review
  5. 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

14 authors at 2 institutions in 2 countries.

Chinatsu MukaiBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA. cmk53@cornell.edu.ORCID http://orcid.org/0000-0003-0080-9371
Eunju ChoiDepartment of Biomedical Sciences, Section of Anatomic Pathology, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Kelly L SamsBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Elena Zu KlampenBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Lynne AnguishBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Brooke A MarksBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Edward J RiceBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Zhong WangBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Lauren A ChoateBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Shao-Pei ChouBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Yukinari KatoDepartment of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Andrew D MillerDepartment of Biomedical Sciences, Section of Anatomic Pathology, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Charles G DankoBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Scott A CoonrodBaker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Cornell University · USTohoku University · JP

Funding

Baker Institute Internal grant dog3ClancysCure NACornell Research Animal Health grant NAJapan Agency for Medical Research and Development (JP) JP19am0401013, JP19am0101078, JP19ae0101028Judy and Fred Wilpon Family Foundation NAKyle's Legacy Inc NAMr. Jake Holshuh NAMrs. Alice C. Sinclair NA
6 · The paper itself

Abstract

backgroundCanine visceral hemangiosarcoma (HSA) is a highly aggressive cancer of endothelial origin that closely resembles visceral angiosarcoma in humans, both clinically and histopathologically. Currently there is an unmet need for new diagnostics and therapies for both forms of this disease. The goal of this study was to utilize Chromatin run-on sequencing (ChRO-seq) and immunohistochemistry (IHC) to identify gene and protein expression signatures that may be important drivers of HSA progression.

resultsChRO-seq was performed on tissue isolated from 17 HSA samples and 4 normal splenic samples. Computational analysis was then used to identify differentially expressed genes and these factors were subjected to gene ontology analysis. ChRO-seq analysis revealed over a thousand differentially expressed genes in HSA tissue compared with normal splenic tissue (FDR < 0.005). Interestingly, the majority of genes overexpressed in HSA tumor tissue were associated with extracellular matrix (ECM) remodeling. This observation correlated well with our histological analysis, which found that HSA tumors contain a rich and complex collagen network. Additionally, we characterized the protein expression patterns of two highly overexpressed molecules identified in ChRO-seq analysis, podoplanin (PDPN) and laminin alpha 4 (LAMA4). We found that the expression of these two ECM-associated factors appeared to be largely limited to transformed endothelial cells within the HSA lesions.

conclusionOutcomes from this study suggest that ECM remodeling plays an important role in HSA progression. Additionally, our study identified two potential novel biomarkers of HSA, PDPN and LAMA4. Interestingly, given that function-blocking anti-PDPN antibodies have shown anti-tumor effects in mouse models of canine melanoma, our studies raise the possibility that these types of therapeutic strategies could potentially be developed for treating canine HSA.

Indexed as

AnimalsBiomarkers, TumorChromatinChromosome MappingDog DiseasesDogsExtracellular MatrixGene Expression Regulation, NeoplasticGene OntologyHemangiosarcomaMembrane GlycoproteinsSpleenSplenic NeoplasmsBiomarkers, TumorChromatinMembrane GlycoproteinsChRO-seqCollagenECMHemangiosarcomaLAMA4PDPN

Identifiers

PMID32571313
PMCPMC7310061
OpenAlexW3036545314

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.