Gene expression profiles of beta-adrenergic receptors in canine vascular tumors: a preliminary study.


Journal

BMC veterinary research
ISSN: 1746-6148
Titre abrégé: BMC Vet Res
Pays: England
ID NLM: 101249759

Informations de publication

Date de publication:
30 May 2022
Historique:
received: 23 02 2022
accepted: 18 05 2022
entrez: 31 5 2022
pubmed: 1 6 2022
medline: 3 6 2022
Statut: epublish

Résumé

Beta adrenergic receptors (β-AR) play a key role in regulating several hallmark pathways of both benign and malignant human and canine tumors. There is scarce information on the expression of β-AR in canine vascular tumors. Therefore, the purpose of the present research work was to study the mRNA expression levels of the three subtypes of the β-AR genes (ADRB1, ADRB2, ADRB3) in hemangiosarcoma (HSA) and hemangioma (HA), as well as in vascular hamartomas (VH) from dogs.Fifty samples (n = 50) were obtained from 38 dogs. Twenty-three animals had HSA, eight animals HA and seven animals VH. HSA were auricular (n = 8), splenic (n = 5), cutaneous (n = 6), auricular and splenic (n = 2), cutaneous-muscular (n = 1) and disseminated (n = 1). There were seven cases of HSA that were divided into primary tumor and secondary (metastatic) tumor. Skin and muscle samples with a normal histological study were used as control group. ADRB gene expression was determinate in all samples by real-time quantitative PCR. Results showed that ADRB1, ADRB2 and ADRB3 were overexpressed in HSA when compared to the control group. ADRB2 was overexpressed in HA when compared to the control group. HSA express higher values of ADBR1 (p = 0.0178) compared to VH. There was a high inter-individual variability in the expression of the three subtypes of ADBR. No statistically significant difference in the expression of ADBR genes were observed between HSA primary when compared to metastatic or in different anatomical locations. In conclusion, canine HSA overexpress the three β-AR subtypes and canine HA β2-AR. High variability was observed in β-AR mRNA levels amongst HSA cases.

Identifiants

pubmed: 35637463
doi: 10.1186/s12917-022-03317-1
pii: 10.1186/s12917-022-03317-1
pmc: PMC9150297
doi:

Substances chimiques

RNA, Messenger 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

206

Informations de copyright

© 2022. The Author(s).

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Auteurs

Jordi Clanxet (J)

Department of Animal Medicine and Surgery, Universitat Autònoma de Barcelona, 08193, Barcelona, Spain.

Mariana Teles (M)

Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, 08193, Barcelona, Spain.
Institute of Biotechnology and Biomedicine, Universitat Autònoma de Barcelona, 08193, Barcelona, Spain.

Javier Hernández-Losa (J)

Molecular Biology Laboratory, Department of Pathology, Hospital Universitario Vall d'Hebron, Passeig Vall d´Hebron, 119-129, 08035, Barcelona, Spain.

Manuel Ruiz-Echarri Rueda (MR)

Bristol Royal Infirmary, Marlborough Street, Bristol, BS2 8HW, UK.

Luis Benitez-Fusté (L)

Hospital Veterinari del Mar, C/ Marina 69, 08005, Barcelona, Spain.

Josep Pastor (J)

Department of Animal Medicine and Surgery, Universitat Autònoma de Barcelona, 08193, Barcelona, Spain. josep.pastor@uab.cat.

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Classifications MeSH