Immunohistochemical study of angiogenesis and angiogenic factors in equine granulosa cell tumours.
Abstract: The first part of our study (Müller et al., 2009) characterized angiogenesis in the equine cycling ovary through histomorphological and immunohistochemical examinations (vascular endothelial growth factors A and B [VEGF A, VEGF B], vascular endothelial growth factor receptors 1 and 2 [VEGF-R1, VEGF-R2], vascular angiopoietins 1 and 2 [Ang1, Ang2], angiopoietin receptor [Tie2], and von Willebrand Factor). Since angiogenesis plays an important role in development and growth of numerous tumours, the second part of our study involved a similar examination of 70 equine granulosa cell tumours (GCTt). The results of the second study were compared with those of the normal equine ovary. Certain similarities in the expression pattern could be detected between normal, cyclical ovaries (Müller et al., 2009) and GCTt. The immunoreactivity of granulosa cells and Leydig-like cells in GCTt resembles granulosa cells and luteinized thecal cells in periovulatory cycling ovaries. The neoplastic cells support circulation, supply and growth of GCTt by contributing to angiogenesis.
Copyright © 2011 Elsevier Ltd. All rights reserved.
Publication Date: 2011-04-14 PubMed ID: 21492887DOI: 10.1016/j.rvsc.2011.02.016Google Scholar: Lookup
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- Journal Article
Summary
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This research focuses on assessing angiogenesis and angiogenic factors in horse granulosa cell tumors (GCTt), with results compared to that of normal horse ovaries.
Study Overview
- The study was conducted in two parts: The first part characterized angiogenesis, the process through which new blood vessels are formed, in the equine cycling ovary. This was done through histomorphological and immunohistochemical examinations, taking into account various factors related to vascular growth.
- The second part employed similar examination techniques to study 70 equine granulosa cell tumours (GCTt). GCTts are a type of ovarian tumor that occurs in horses, and this part of the study involved understanding the role of angiogenesis in the development of these tumors.
Key Findings
- Certain similarities in the expression pattern were detected between normal, cyclical ovaries and GCTt. Such similarities were seen in terms of the behavior of angiogenic factors as well as cellular characteristics.
- The research found that the immunoreactivity of granulosa cells and Leydig-like cells in GCTt resembles that of granulosa cells and luteinized thecal cells in periovulatory cycling ovaries. This means the tumour cells displayed similar immunological responses as typical ovary cells during ovulation, hinting at possible similar physiological processes at play.
- The study concluded that the neoplastic, or tumour, cells support their circulation, supply and growth by contributing to angiogenesis. This is significant as it sheds light on the supporting structures that allow these tumors to grow and thrive.
Implications
- By understanding the role of angiogenesis in ovarian tumors in horses, researchers may be better equipped to develop strategies for managing or treating such conditions. The findings could have implications for not only veterinary medicine, but possibly human medicine as well, given the pathological similarities between ovarian tumours in horses and humans.
- The similarities in expression patterns between normal ovaries and GCTt may also lend insights into the pathogenesis of these tumours and provide targets for future therapeutic interventions.
- This research emphasises the importance of angiogenesis in tumour growth and suggests possible therapeutic directions focused on interfering with angiogenesis.
Cite This Article
APA
Müller K, Ellenberger C, Hoppen HO, Schoon HA.
(2011).
Immunohistochemical study of angiogenesis and angiogenic factors in equine granulosa cell tumours.
Res Vet Sci, 92(3), 471-477.
https://doi.org/10.1016/j.rvsc.2011.02.016 Publication
Researcher Affiliations
- Institute of Pathology, Faculty of Veterinary Medicine, University of Leipzig, An den Tierkliniken 33, 04103 Leipzig, Germany. kristin.mueller@vetmed.uni-leipzig.de
MeSH Terms
- Angiogenesis Inducing Agents / metabolism
- Animals
- Female
- Gene Expression Regulation, Neoplastic / physiology
- Granulosa Cell Tumor / blood supply
- Granulosa Cell Tumor / metabolism
- Granulosa Cell Tumor / pathology
- Granulosa Cell Tumor / veterinary
- Horse Diseases / metabolism
- Horse Diseases / pathology
- Horses
- Neovascularization, Pathologic / metabolism
- Neovascularization, Pathologic / veterinary
Citations
This article has been cited 7 times.- Zhao X, Hu J, Li J, Gu L, Chen J, Othmane B, Gong G, Yuan J, Deng H. THEM6: A Novel Molecular Biomarker Predicts Tumor Microenvironment, Molecular Subtype, and Prognosis in Bladder Cancer. Dis Markers 2022;2022:7147279.
- Zhao X, Tang Y, Ren H, Lei Y. Identification of Prognosis-Related Genes in Bladder Cancer Microenvironment across TCGA Database. Biomed Res Int 2020;2020:9143695.
- Bussche L, Van de Walle GR. Peripheral Blood-Derived Mesenchymal Stromal Cells Promote Angiogenesis via Paracrine Stimulation of Vascular Endothelial Growth Factor Secretion in the Equine Model. Stem Cells Transl Med 2014 Dec;3(12):1514-25.
- Lessiak U, Melchert M, Walter I, Kummer S, Nell B, Tschulenk W, Pratscher B. Isolation-protocol, characterization, and in-vitro performance of equine umbilical vein endothelial cells. Front Vet Sci 2024;11:1421946.
- Wolf N, Hahn JA, Walter I, Zablotski Y, Zerbe H, Witte TS. Pathohistological Findings after Bilateral Ovariectomy in Mares with Behavioral Problems. Animals (Basel) 2024 Oct 8;14(19).
- Peng X, Liu C, Zhang L, Chen Y, Mao L, Gao S, Shi X, Zuo L. IL4I1: a novel molecular biomarker represents an inflamed tumor microenvironment and precisely predicts the molecular subtype and immunotherapy response of bladder cancer. Front Pharmacol 2024;15:1365683.
- Lessiak U, Pratscher B, Tichy A, Nell B. Bevacizumab Efficiently Inhibits VEGF-Associated Cellular Processes in Equine Umbilical Vein Endothelial Cells: An In Vitro Characterization. Vet Sci 2023 Oct 26;10(11).
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