Expression of Vimentin, α-SMA, and CD34 in Malignant Mammary Tumors in Dogs
https://doi.org/10.23947/2949-4826-2026-25-2-54-60
EDN: GIVVOK
Abstract
Introduction. At the contemporary stage of mammary tumor studies, the microenvironment is considered a key factor contributing to neoplasia formation and metastasis. Therefore, the greatest attention is paid to the cellular composition of the mammary tumor microenvironment, in which the most widespread elements are the stromal cancer-associated fibroblasts (CAFs). However, in veterinary oncology, stromal markers of malignant mammary tumors are insufficiently studied. The aim of the present study is to investigate the expression of tumor marker proteins, i.e. vimentin, α-SMA, and CD34, in the stroma of the malignant mammary tumor microenvironments in dogs.
Materials and Methods. The objects of the study that was conducted in the period from 2022 to 2024 were the female dogs of various breeds and ages (n=26). The materials studied were the mammary tumors. A comprehensive range of histological and immunohistochemical studies was conducted in compliance with the standard techniques.
Results. It has been established that in different histological types and degrees of canine mammary tumor malignancy, the fibroblastic differentiation lineage cells demonstrate a high expression of vimentin and α-SMA and a low expression of CD34, which indicates their differentiation into CAFs.
Discussion and Conclusion. The obtained results can be used as basic applied data in the study of carcinogenesis in veterinary oncology.
Keywords
About the Authors
A. A. DarbishevaRussian Federation
Alina A. Darbisheva, Post Graduate Degree Student of the Parasitology and Veterinary-Sanitary Inspection, Anatomy and Pathoanatomy Department Named after S.N. Nikolsky
12, Zootechnichesky Lane, Stavropol, 355017
O. V. Dilekova
Russian Federation
Olga V. Dilekova, Dr.Sci. (Biology), Associate Professor of the Parasitology and Veterinary-Sanitary Inspection, Anatomy and Pathoanatomy Department Named after S.N. Nikolsky
12, Zootechnichesky Lane, Stavropol, 355017
References
1. Place AE, Huh SJ, Polyak K. The Microenvironment in Breast Cancer Progression: Biology and Implications for Treatment. Breast Cancer Research. 2011;13:227. https://doi.org/10.1186/bcr2912
2. Mehraj U, Dar AH, Wani NA, Mir MA. Tumor Microenvironment Promotes Breast Cancer Chemoresistance. Cancer Chemother Pharmacol. 2021;87:147–158. https://doi.org/10.1007/s00280-020-04222-w
3. Yu T, Di G. Role of Tumor Microenvironment in Triple-Negative Breast Cancer and Its Prognostic Significance. Chinese Journal of Cancer Research. 2017;29(3):237–252. https://doi.org/10.21147/j.issn.1000-9604.2017.03.10
4. Li JJ, Tsang JY, Tse MG. Tumor Microenvironment in Breast Cancer—Updates on Therapeutic Implications and Pathologic Assessment. Cancers. 2021;13(16):4233. https://doi.org/10.3390/cancers13164233
5. Giorello MB, Borzone FR, Labovsky V, Piccioni FV, Chasseing NA. Cancer-Associated Fibroblasts in the Breast Tumor Microenvironment. Journal of Mammary Gland Biology and Neoplasia. 2021;26:135–155. https://doi.org/10.1007/s10911-020-09475-y
6. Chen Z, Fang Z, Ma J. Regulatory Mechanisms and Clinical Significance of Vimentin in Breast Cancer. Biomedi-cine and Pharmacotherapy. 2021;133:111068. https://doi.org/10.1016/j.biopha.2020.111068
7. Han C, Liu T, Yin R. Biomarkers for Cancer-Associated Fibroblasts. Biomarker Research. 2020;8:64. https://doi.org/10.1186/s40364-020-00245-w
8. Dominguez R, Holmes KC. Actin structure and function. Annual Review of Biophysics. 2011;40:169–186. https://doi.org/10.1146/annurev-biophys-042910-155359
9. Yoshimura H, Michishita M, Ohkusu-Tsukada K, Takahashi K. Increased Presence of Stromal Myofibroblasts and Tenascin-C with Malignant Progression in Canine Mammary Tumors. Veterinary Pathology. 2010;48(1):313–321. https://doi.org/10.1177/0300985810369901
10. Radu P, Zurzu M, Paic V, Bratucu M, Garofil D, Tigora A, et al. CD34—Structure, Functions and Relationship with Cancer Stem Cells . Medicina. 2023;59(5):938. https://doi.org/10.3390/medicina59050938
11. Sidney LE, Branch MJ, Dunphy SE, Dua HS, Hopkinson A. Concise Review: Evidence for CD34 as a Common Marker for Diverse Progenitors. Stem Cells. 2014;32(6):1380–1389. https://doi.org/10.1002/stem.1661
12. Catteau X, Simon P, Noël JC. Myofibroblastic Stromal Reaction and Lymph Node Status in Invasive Breast Carcinoma: Possible Role of the TGF- β1/TGF- βR1 Pathway. BMC Cancer. 2014;14:499. https://doi.org/10.1186/1471-2407-14-499
13. Díaz-Flores L, Gutiérrez R, González-Gómez M, García MP, Díaz-Flores L, Carrasco JL, et al. CD34+ Stromal Cells/Telocytes as a Source of Cancer-Associated Fibroblasts (CAFs) in Invasive Lobular Carcinoma of the Breast. In-ternational Journal of Molecular Sciences. 2021;22(7):3686. https://doi.org/10.3390/ijms22073686
14. Khan AA, Alam K, Harris Н. A Clinicopathological Study of CD34 Antigen Expression in Benign and Malignant Breast Lesions. Journal of Clinical and Experimental Pathology. 2017;07(04). https://doi.org/10.4172/2161-0681.1000321
Review
For citations:
Darbisheva A.A., Dilekova O.V. Expression of Vimentin, α-SMA, and CD34 in Malignant Mammary Tumors in Dogs. Russian Journal of Veterinary Pathology. 2026;25(2):54-60. https://doi.org/10.23947/2949-4826-2026-25-2-54-60. EDN: GIVVOK
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