The Impact of Excision Interval on Equine Melanoma Progression: Time Matters?
Abstract: Equine melanomas are a common neoplasm in gray horses. However, scientific knowledge about their progression over time is quite scarce. Some owners and veterinarians still believe that early intervention is not necessary, stating that tumors evolve very slowly and intervention could worsen the animal's condition. This work aims to identify clinical and histological differences that may exist between equine melanomas with different excision intervals (time between tumor detection and surgical excision). A total of 42 tumors (13 benign and 29 malignant) from 34 horses were included in this study. There was a statistically significant association between excision interval and tumor size (p = 0.038), with tumors excised later being significantly larger than the ones excised sooner. The excision interval was also statistically associated with the number of tumors (p = 0.011), since the horses that carried a tumor for longer seemed to be prone to have multiple tumors. Furthermore, there was an association between excision interval and malignancy (p = 0.035), with tumor excised later being fives times more likely to be malignant. This study provides evidence of delayed excision's effect on the progression of equine melanomas. Additionally, it reinforces the importance of the early excision of these tumors.
Publication Date: 2024-04-22 PubMed ID: 38672392PubMed Central: PMC11047369DOI: 10.3390/ani14081244Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
- Journal Article
Summary
This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.
This research investigates whether the timing of surgical removal affects the progression of melanoma tumors in horses. The study concludes that delaying the removal of these tumors is associated with increased tumor size, the presence of multiple tumors, and an increased likelihood of the tumors being malignant.
Background
- Equine melanomas are a common type of cancer in gray horses. While these cancers are known to progress slowly, there is limited scientific knowledge about how cancer progression might vary depending on how long the tumor is left in place before surgical removal.
- Some horse owners and veterinarians believe that early intervention may not be necessary or could even potentially worsen the horse’s condition. However, no data are officially established to authenticate these beliefs until now.
Aim of the Study
- The study was conducted to identify any clinical and histological differences that might exist between horse melanomas that are removed at different times (measured as the ‘excision interval’, or the time between tumor detection and surgical removal).
Study Design and Population
- The research included a total of 42 tumors (13 benign and 29 malignant) from 34 horses.
Key Findings
- The study found a statistically significant link between the length of the excision interval and the size of the tumor, with tumors that were removed later being significantly larger than those removed earlier.
- The amount of time a horse had a tumor was also found to correlate statistically with the number of tumors, with horses that had a tumor for a longer period being more likely to have multiple tumors.
- Finally, the excision interval was found to be statistically associated with malignancy, with tumors removed later being five times more likely to be malignant. Hence proving that the longer a tumor remains, the higher the chance it has of becoming cancerous.
Conclusion of the Study
- This research provides evidence suggesting that delaying excision can impact the progression of equine melanomas. It also supports the idea that early removal of these tumors is essential to control its growth and malignity.
Cite This Article
APA
Pimenta J, Prada J, Pires I, Cotovio M.
(2024).
The Impact of Excision Interval on Equine Melanoma Progression: Time Matters?
Animals (Basel), 14(8).
https://doi.org/10.3390/ani14081244 Publication
Researcher Affiliations
- CECAV-Veterinary and Animal Research Center, University of Trás-os-Montes e Alto Douro, 5000-801 Vila Real, Portugal.
- Associate Laboratory for Animal and Veterinary Sciences (AL4AnimalS), 5000-801 Vila Real, Portugal.
- CIVG-Vasco da Gama Research Center, EUVG-Vasco da Gama University School, 3020-210 Coimbra, Portugal.
- CECAV-Veterinary and Animal Research Center, University of Trás-os-Montes e Alto Douro, 5000-801 Vila Real, Portugal.
- Associate Laboratory for Animal and Veterinary Sciences (AL4AnimalS), 5000-801 Vila Real, Portugal.
- Veterinary Sciences Department, University of Trás-os-Montes e Alto Douro, 5000-801 Vila Real, Portugal.
- CECAV-Veterinary and Animal Research Center, University of Trás-os-Montes e Alto Douro, 5000-801 Vila Real, Portugal.
- Associate Laboratory for Animal and Veterinary Sciences (AL4AnimalS), 5000-801 Vila Real, Portugal.
- Veterinary Sciences Department, University of Trás-os-Montes e Alto Douro, 5000-801 Vila Real, Portugal.
- CECAV-Veterinary and Animal Research Center, University of Trás-os-Montes e Alto Douro, 5000-801 Vila Real, Portugal.
- Associate Laboratory for Animal and Veterinary Sciences (AL4AnimalS), 5000-801 Vila Real, Portugal.
- Veterinary Sciences Department, University of Trás-os-Montes e Alto Douro, 5000-801 Vila Real, Portugal.
- Faculty of Veterinary Medicine, Lusófona University, Campo Grande 376, 1749-024 Lisbon, Portugal.
Grant Funding
- UIDB/00772/2020 / Fundação para a Ciência e Tecnologia
Conflict of Interest Statement
The authors declare no conflicts of interest.
References
This article includes 46 references
- Knottenbelt DC, Patterson-Kane JC, Snalune KL. Melanocytic Neoplasms. Elsevier; Amsterdam, The Netherlands: 2015. pp. 237–246.
- Phillips JC, Lembcke LM. Equine Melanocytic Tumors. Vet. Clin. N. Am. Equine Pract. 2013;29:673–687.
- Sullins KE. Melanocytic Tumours in Horses. Equine Vet. Educ. 2020;32:624–630.
- Valentine BA. The Spectrum of Equine Melanocytic Tumours. Equine Vet. Educ. 2003;15:24.
- Seltenhammer MH, Simhofer H, Scherzer S, Zechner P, Curik I, Sölkner J, Brandt SM, Jansen B, Pehamberger H, Eisenmenger E. Equine Melanoma in a Population of 296 Grey Lipizzaner Horses. Equine Vet. J. 2003;35:153–157.
- Valentine BA. Equine Melanocytic Tumors: A Retrospective Study of 5 3 Horses (1988 to 1991). J. Vet. Intern. Med. 1995;95:291–297.
- Moore JS, Shaw C, Shaw E, Buechner-Maxwell V, Scarratt WK, Crisman M, Furr M, Robertson J. Melanoma in Horses: Current Perspectives. Equine Vet. Educ. 2013;25:144–151.
- Rosengren Pielberg G, Golovko A, Sundström E, Curik I, Lennartsson J, Seltenhammer MH, Druml T, Binns M, Fitzsimmons C, Lindgren G. A Cis-Acting Regulatory Mutation Causes Premature Hair Graying and Susceptibility to Melanoma in the Horse. Nat. Genet. 2008;40:1004–1009.
- Cavalleri JMV, Mählmann K, Steinig P, Feige K. Aetiology, Clinical Presentation and Current Treatment Options of Equine Malignant Melanoma—A Review of the Literature. Pferdeheilkunde 2014;30:455–460.
- Curik I, Druml T, Seltenhammer M, Sundström E, Pielberg GR, Andersson L, Sölkner J. Complex Inheritance of Melanoma and Pigmentation of Coat and Skin in Grey Horses. PLoS Genet. 2013;9:e1003248.
- Teixeira RBC, Rendahl AK, Anderson SM, Mickelson JR, Sigler D, Buchanan BR, Coleman RJ, Mccue ME. Coat Color Genotypes and Risk and Severity of Melanoma in Gray Quarter Horses. J. Vet. Intern. Med. 2013;27:1201–1208.
- Foley G, Valentine B, Kincaid A. Congenital and Acquired Melanocytomas (Benign Melanomas) in Eighteen Young Horses. Vet. Pathol. 1991;28:363–369.
- Pimenta J, Prada J, Cotovio M. Equine Melanocytic Tumors: A Narrative Review. Animals 2023;13:247.
- Knottenbelt DC, Patterson-Kane JC, Snalune KL. Tumours of the Skin. Elsevier; Amsterdam, The Netherlands: 2015. pp. 544–584.
- Knottenbelt D, Croft J. The Equine Melanoma. Equine Health 2018;18:30–32.
- Pilsworth RC, Knottenbelt D. Skin Diseases Refresher Melanoma. Equine Vet. Educ. 2006;18:296–297.
- Knottenbelt DC, Patterson-Kane JC, Snalune KL. Principles of Diagnosis. Elsevier; Amsterdam, The Netherlands: 2015. pp. 85–107.
- Knottenbelt DC, Patterson-Kane JC, Snalune KL. The Challenges and Problems of Equine Oncological Practice. Elsevier Health Sciences; New York, NY, USA: 2015. pp. 7–10.
- Billi T, Karadima V, Tyrnenopoulou P, Apostolopoulou EP, Brellou GD, Diakakis N. Surgical Excision of a Malignant Metastatic Melanoma Located in a Skeletal Muscle of the Lateral Thorax of a Horse. Vet. Med. Sci. 2021;7:297–302.
- Groom LM, Sullins KE. Surgical Excision of Large Melanocytic Tumours in Grey Horses: 38 Cases (2001–2013). Equine Vet. Educ. 2018;30:438–443.
- Nishiya AT, Massoco CO, Felizzola CR, Perlmann E, Batschinski K, Tedardi MV, Garcia JS, Mendonça PP, Teixeira TF, Dagli MLZ. Comparative Aspects of Canine Melanoma. Vet. Sci. 2016;3:7.
- Resende L, Moreira J, Prada J, Queiroga FL, Pires I. Melanoma—Current Clinical Management and Future Therapeutics. Intech; Rijeka, Croatia: 2015.
- Wong K, van der Weyden L, Schott CR, Foote A, Constantino-Casas F, Smith S, Dobson JM, Murchison EP, Wu H, Yeh I. Cross-Species Genomic Landscape Comparison of Human Mucosal Melanoma with Canine Oral and Equine Melanoma. Nat. Commun. 2019;10:353.
- Seltenhammer MH, Heere-Ress E, Brandt S, Druml T, Jansen B, Pehamberger H, Niebauer GW. Comparative Histopathology of Grey-Horse-Melanoma and Human Malignant Melanoma. Pigment Cell Res. 2004;17:674–681.
- Burden K. Melanomas and Their Effect on the Grey Horse. Young Sci. J. 2011;4:75.
- Johnson P. Dermatologic Tumours (Excluding Sarcoids). Vet. Clin. N. Am. Equine Pract. 1998;14:625–658.
- Deleon M. Cutaneous Melanoma: A Comparative Study between Gray Horses, Canines, and Humans. Iowa State University; Ames, IA, USA: 2021.
- Macgillivray KC, Sweeney RW, Piero F. Metastatic Melanoma in Horses. J. Vet. Intern. Med. 2002;16:452–456.
- Hatai H, Hatazoe T, Seo H, Tozaki T, Ishikawa S, Miyoshi N, Misumi K, Hobo S. Primary Sinonasal Malignant Melanoma with Systemic Metastasis in a Non-Gray Horse. J. Vet. Diagn. Investig. 2021;33:379–383.
- Rodríguez F, Forga J, Herráez P, Andrada M, Fernández A. Metastatic Melanoma Causing Spinal Cord Compression in a Horse. Vet. Rec. 1998;142:248–249.
- Patterson-Kane JC, Sanchez LC, Uhl EW, Edens LM. Disseminated Metastatic Intramedullary Melanoma in an Aged Grey Horse. J. Comp. Pathol. 2001;125:204–207.
- Szweda M, Rychlik A, Babińska I, Pomianowski A. Significance of Cyclooxygenase-2 in Oncogenesis. J. Vet. Res. 2019;63:215–224.
- Goulet AC, Einsphar JG, Alberts DS, Beas A, Burk C, Bhattacharyya A, Bangert J, Harmon JM, Fujiwara H, Koki A. Analysis of Cyclooxygenase 2 (COX-2) Expression during Malignant Melanoma Progression. Cancer Biol. Ther. 2003;2:713–718.
- Rao DS, Gui D, Koski ME, Popoviciu LM, Wang H, Reiter RE, Said JW. An Inverse Relation between COX-2 and E-Cadherin Expression Correlates with Aggressive Histologic Features in Prostate Cancer. Appl. Immunohistochem. Mol. Morphol. 2006;14:375–383.
- Silvestri S, Porcellato I, Mechelli L, Menchetti L, Iussich S, De Maria R, Sforna M, Bongiovanni L, Brachelente C. E-Cadherin Expression in Canine Melanocytic Tumors: Histological, Immunohistochemical, and Survival Analysis. Vet. Pathol. 2020;57:608–619.
- Han JI, Kim Y, Kim DY, Na KJ. Alteration in E-Cadherin/β-Catenin Expression in Canine Melanotic Tumors. Vet. Pathol. 2013;50:274–280.
- Silveira TL, Pang LY, Di Domenico A, Veloso ES, Silva ILD, Puerto HLD, Ferreria E, Argyle DJ. COX-2 Silencing in Canine Malignant Melanoma Inhibits Malignant Behaviour. Front. Vet. Sci. 2021;8:633170.
- Tudor DV, Bâldea I, Lupu M, Kacso T, Kutasi E, Hopârtean A, Stretea R, Filip AG. COX-2 as a Potential Biomarker and Therapeutic Target in Melanoma. Cancer Biol. Med. 2020;17:20–31.
- Kuphal S, Poser I, Jobin C, Hellerbrand C, Bosserhoff AK. Loss of E-Cadherin Leads to Upregulation of NFκB Activity in Malignant Melanoma. Oncogene 2004;23:8509–8519.
- Dohadwala M, Yang SC, Luo J, Sharma S, Batra RK, Huang M, Lin Y, Goodglick L, Krysan K, Fishbein MC. Cyclooxygenase-2-Dependent Regulation of E-Cadherin: Prostaglandin E 2 Induces Transcriptional Repressors ZEB1 and Snail in Non-Small Cell Lung Cancer. Cancer Res. 2006;66:5338–5345.
- Jang TJ, Jeon KH, Jung KH. Cyclooxygenase-2 Expression Is Related to the Epithelial-to-Mesenchymal Transition in Human Colon Cancers. Yonsei Med. J. 2009;50:818–824.
- Sitarz R, Leguit RJ, De Leng WWJ, Morsink FHM, Polkowski WP, Maciejewski R, Offerhaus GJA, Milne AN. Cyclooxygenase-2 Mediated Regulation of E-Cadherin Occurs in Conventional but Not Early-Onset Gastric Cancer Cell Lines. Cell. Oncol. 2009;31:475–485.
- Campagne C, Julé S, Bernex F, Estrada M, Aubin-Houzelstein G, Panthier J, Egidy G. RACK1, a Clue to the Diagnosis of Cutaneous Melanomas in Horses. BMC Vet. Res. 2012;8:95.
- Queiroga FL, Pires I, Lobo L, Lopes CS. The Role of Cox-2 Expression in the Prognosis of Dogs with Malignant Mammary Tumours. Res. Vet. Sci. 2010;88:441–445.
- Pires I, Garcia A, Prada J, Queiroga FL. COX-1 and COX-2 Expression in Canine Cutaneous, Oral and Ocular Melanocytic Tumours. J. Comp. Pathol. 2010;143:142–149.
- Rowe EL, Sullins KE. Excision as Treatment of Dermal Melanomatosisin Horses: 11 Cases (1994–2000). J. Am. Vet. Med. Assoc. 2004;225:94–96.
Use Nutrition Calculator
Check if your horse's diet meets their nutrition requirements with our easy-to-use tool Check your horse's diet with our easy-to-use tool
Talk to a Nutritionist
Discuss your horse's feeding plan with our experts over a free phone consultation Discuss your horse's diet over a phone consultation
Submit Diet Evaluation
Get a customized feeding plan for your horse formulated by our equine nutritionists Get a custom feeding plan formulated by our nutritionists