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American journal of veterinary research2012; 73(2); 272-278; doi: 10.2460/ajvr.73.2.272

Evaluation of tyrosinase expression in canine and equine melanocytic tumors.

Abstract: To determine the tissue-restricted expression pattern of tyrosinase mRNA in canine and equine melanocytic tumors and relative tyrosinase and major histocompatibility complex (MHC) I mRNA expression in variants of melanocytic tumors. Methods: 39 canine and 8 equine tumor samples and 10 canine and 6 equine normal tissue samples. Methods: RNA was isolated from formalin-fixed, paraffin-embedded tissues. Real-time PCR assays were designed to amplify canine and equine tyrosinase, S18 ribosomal RNA, and major histocompatibility complex I transcripts. Relative expression was determined by use of S18 as a reference and comparison with pigmented and nonpigmented normal tissues. Results: High tyrosinase expression was found in all melanocytic tumors, compared with normal tissues, and expression had no correlation with presence or absence of tumor pigmentation. No significant difference in tyrosinase expression was found among histologic variants of melanocytic tumors. No correlation was found between MHC I and tyrosinase expression or tissue histologic classification. Conclusions: In the present study, the methods used were highly sensitive and specific for detection of tyrosinase expression in equine and canine tumors, and overexpression of this transcript in melanomas was detected. This suggested that a DNA vaccine developed for use in dogs with melanoma that targets tyrosinase may be considered for use in other affected species, such as horses.
Publication Date: 2012-01-28 PubMed ID: 22280389DOI: 10.2460/ajvr.73.2.272Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article discusses evaluating the expression of tyrosinase, a critical enzyme in melanin synthesis, in melanocytic tumors in canines and equines, and its implications for future vaccine development.

Overview of the Research

The study involves the evaluation of tyrosinase mRNA expression in melanocytic tumors of dogs and horses. The tumors were compared to normal tissue samples from both species. The evaluation also included checking for the relative expression of tyrosinase and Major Histocompatibility Complex I (MHC I) mRNA in various types of these tumors.

  • The researchers used 39 canine and 8 equine tumor samples, along with 10 canine and 6 equine normal tissue samples.
  • RNA was isolated from these samples, which were formalin-fixed and paraffin-embedded.
  • Real-time PCR assays were used to amplify the tyrosinase, S18 ribosomal RNA, and MHC I transcripts in canine and equine models.

Findings of the Study

The results from these analyses brought forward several notable observations.

  • There was high expression of tyrosinase in all melanocytic tumors, which was significantly more than in normal tissues.
  • This expression was not associated with the presence or absence of tumor pigmentation. This suggests that the overproduction of tyrosinase occurs regardless of the visual manifestation of melanin in the tumor.
  • There was no significant difference in tyrosinase expression between the different histologic variants of melanocytic tumors.
  • No correlation was found between MHC I and tyrosinase expression or the histologic classification of the tissue.

Conclusions and Implications

The conclusion drawn from this study indicates that the methods used for detecting tyrosinase expression in canine and equine tumors were both sensitive and specific. The observed overexpression of tyrosinase in melanomas may be a critical factor in developing treatments.

  • The study suggests that a DNA vaccine currently being developed with a target on tyrosinase for use in dogs with melanoma could potentially be considered for other species with similar conditions, including horses.
  • This finding opens up possibilities for cross-species application of cancer treatments, potentially providing a larger scope for addressing melanomas affecting various species.

Cite This Article

APA
Phillips JC, Lembcke LM, Noltenius CE, Newman SJ, Blackford JT, Grosenbaugh DA, Leard AT. (2012). Evaluation of tyrosinase expression in canine and equine melanocytic tumors. Am J Vet Res, 73(2), 272-278. https://doi.org/10.2460/ajvr.73.2.272

Publication

ISSN: 1943-5681
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 73
Issue: 2
Pages: 272-278

Researcher Affiliations

Phillips, Jeffrey C
  • Veterinary Teaching Hospital, Department of Small Animal Clinical Sciences, College of Veterinary Medicine, University of Tennessee, Knoxville, 37996, USA. jphill35@me.com
Lembcke, Luis M
    Noltenius, Christina E
      Newman, Shelley J
        Blackford, James T
          Grosenbaugh, Deborah A
            Leard, A Timothy

              MeSH Terms

              • Animals
              • Cancer Vaccines / immunology
              • Dog Diseases / enzymology
              • Dog Diseases / metabolism
              • Dogs
              • Gene Expression Regulation, Enzymologic / physiology
              • Gene Expression Regulation, Neoplastic / physiology
              • Horse Diseases / enzymology
              • Horse Diseases / metabolism
              • Horses
              • Melanoma / metabolism
              • Melanoma / prevention & control
              • Melanoma / veterinary
              • Monophenol Monooxygenase / genetics
              • Monophenol Monooxygenase / metabolism
              • RNA, Messenger / genetics
              • RNA, Messenger / metabolism
              • Vaccines, DNA / immunology

              Citations

              This article has been cited 8 times.
              1. Pimenta J, Prada J, Cotovio M. Equine Melanocytic Tumors: A Narrative Review. Animals (Basel) 2023 Jan 10;13(2).
                doi: 10.3390/ani13020247pubmed: 36670786google scholar: lookup
              2. Pellin MA. The Use of Oncept Melanoma Vaccine in Veterinary Patients: A Review of the Literature. Vet Sci 2022 Oct 28;9(11).
                doi: 10.3390/vetsci9110597pubmed: 36356074google scholar: lookup
              3. Weber LA, Delarocque J, Feige K, Kietzmann M, Kalbitz J, Meißner J, Paschke R, Cavalleri JV. Effects of Topically Applied Betulinic Acid and NVX-207 on Melanocytic Tumors in 18 Horses. Animals (Basel) 2021 Nov 13;11(11).
                doi: 10.3390/ani11113250pubmed: 34827981google scholar: lookup
              4. Zuleger CL, Kang C, Ranheim EA, Kurzman ID, Macklin MD, Newton MA, Wolchok JD, Vail DM, Eriksson E, Albertini MR. Pilot study of safety and feasibility of DNA microseeding for treatment of spontaneous canine melanoma. Vet Med Sci 2017 Aug;3(3):134-145.
                doi: 10.1002/vms3.65pubmed: 29067210google scholar: lookup
              5. Lee BH, Neela PH, Kent MS, Zehnder AM. IQGAP1 is an oncogenic target in canine melanoma. PLoS One 2017;12(4):e0176370.
                doi: 10.1371/journal.pone.0176370pubmed: 28445541google scholar: lookup
              6. Schnabel CL, Steinig P, Koy M, Schuberth HJ, Juhls C, Oswald D, Wittig B, Willenbrock S, Murua Escobar H, Pfarrer C, Wagner B, Jaehnig P, Moritz A, Feige K, Cavalleri JM. Immune response of healthy horses to DNA constructs formulated with a cationic lipid transfection reagent. BMC Vet Res 2015 Jun 23;11:140.
                doi: 10.1186/s12917-015-0452-3pubmed: 26100265google scholar: lookup
              7. Mählmann K, Feige K, Juhls C, Endmann A, Schuberth HJ, Oswald D, Hellige M, Doherr M, Cavalleri JM. Local and systemic effect of transfection-reagent formulated DNA vectors on equine melanoma. BMC Vet Res 2015 Jun 11;11:132.
                doi: 10.1186/s12917-015-0422-9pubmed: 26063232google scholar: lookup
              8. Mählmann K, Feige K, Juhls C, Endmann A, Schuberth HJ, Oswald D, Hellige M, Doherr M, Cavalleri JM. Local and systemic effect of transfection-reagent formulated DNA vectors on equine melanoma. BMC Vet Res 2015 May 14;11:107.
                doi: 10.1186/s12917-015-0414-9pubmed: 25967290google scholar: lookup