Peer-reviewed veterinary case report
RNA biomarkers that identify canine epitheliotropic lymphoma
By Olayinka, Jadesola Temitope et al.·Published in Frontiers in veterinary science·2023·Department of Dermatology, United States·View original on PubMed →
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Original publication title: Cathepsin W, T-cell receptor-associated transmembrane adapter 1, lymphotactin and killer cell lectin like receptor K1 are sensitive and specific RNA biomarkers of canine epitheliotropic lymphoma.
- Species:
- dog
Plain-English summary
A group of dogs with a type of skin cancer called canine epitheliotropic lymphoma (EL) was studied to find specific markers that could help diagnose the disease. This lymphoma can be tricky to identify early on because it can look like other skin issues. Researchers found certain RNA markers in skin samples that were unique to EL, which could help vets distinguish it from other skin problems. These findings could lead to better diagnosis and treatment options for dogs with this condition.
People also search for: dog skin cancer symptoms · canine epitheliotropic lymphoma treatment · how to diagnose skin problems in dogs
Abstract
Cutaneous T-cell lymphoma (CTCL) is an uncommon type of lymphoma involving malignant skin-resident or skin-homing T cells. Canine epitheliotropic lymphoma (EL) is the most common form of CTCL in dogs, and it also spontaneously arises from T lymphocytes in the mucosa and skin. Clinically, it can be difficult to distinguish early-stage CTCLs apart from other forms of benign interface dermatitis (ID) in both dogs and people. Our objective was to identify novel biomarkers that can distinguish EL from other forms of ID, and perform comparative transcriptomics of human CTCL and canine EL. Here, we present a retrospective gene expression study that employed archival tissue from biorepositories. We analyzed a discovery cohort of 6 canines and a validation cohort of 8 canines with EL which occurred spontaneously in client-owned companion dogs. We performed comparative targeted transcriptomics studies using NanoString to assess 160 genes from lesional skin biopsies from the discovery cohort and 800 genes from the validation cohort to identify any significant differences that may reflect oncogenesis and immunopathogenesis. We further sought to determine if gene expression in EL and CTCL are conserved across humans and canines by comparing our data to previously published human datasets. Similar chemokine profiles were observed in dog EL and human CTCL, and analyses were performed to validate potential biomarkers and drivers of disease. In dogs, we found enrichment of T cell gene signatures, with upregulation of,,,,,, andin EL in dogs compared to healthy controls. Importantly,,anddistinguished EL from all other forms of interface dermatitis we studied, providing much-needed biomarkers for the veterinary field./were also highly specific of EL in our validation cohort. Future studies exploring the oncogenesis of spontaneous lymphomas in companion animals will expand our understanding of these disorders. Biomarkers may be useful for predicting disease prognosis and treatment responses. We plan to use our data to inform future development of targeted therapies, as well as for repurposing drugs for both veterinary and human medicine.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/38026637/