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Seminal vesicles are important hormone-dependent accessory sex glands. Transgenic adenocarcinoma of the mouse prostate (TRAMP) model has been used to evaluate malignant diseases in the prostate and in other sexual glands. The aim of this study was to characterize structural and molecular features of the seminal vesicle in different life periods of the TRAMP mice. Groups: Control Group (5 FVB/12 week old mice), TRAMP 12 and 22 Groups (10 TRAMP 12 and 22 week old mice, respectively). Seminal vesicles were evaluated by morphological and immunohistochemical parameters; androgenic receptor (AR), Insulin-like growth factor 1 (IGFR-1) and metalloproteinase 9 (MMP-9). The TRAMP mice showed frequent epithelial proliferation, including cellular stromal invasion, especially in the TRAMP 22 group. Intense AR reactivity was seen in both stroma and epithelial regions in the TRAMP 22 group. Intense IGFR-1 and MMP-9 stromal immunolabeling was identified in both TRAMP groups. Thus, there were structural and molecular changes in the seminal vesicle in TRAMP mice, compromising not only the structure but also the stromal signaling, damaging thus the function and leading to glandular lesions. TRAMP mice could be indicated as a good model to study alterations of the seminal vesicle in association to prostate cancer.
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http://dx.doi.org/10.1016/j.tice.2016.03.005 | DOI Listing |
Int J Mol Sci
August 2025
Departamento de Neurobiología Celular y Molecular, Instituto de Neurobiología, Universidad Nacional Autónoma de México, Campus Juriquilla, Querétaro 76230, Mexico.
Advanced prostate cancer frequently develops resistance to antiandrogen therapy and acquires an aggressive neuroendocrine phenotype. Antiandrogens stimulate peroxisome proliferator-activated receptor gamma (PPARG) signaling and cancer progression. Molecular iodine (I) induces cytotoxic effects in prostate cancer cell lines and antineoplastic effects in neuroblastoma and breast cancer through the indirect activation of PPARG.
View Article and Find Full Text PDFSci Rep
July 2025
Prostate Cancer Discovery and Development Program, Thomas Jefferson University, Bluemle Life Sciences Building, 233 South 10th Street Suite 506, Philadelphia, PA, 19107, USA.
It is known that β1 integrins and a downstream signaling molecule c-Src are upregulated in prostate cancer (PrCa) tissues, are co-expressed in circulating small extracellular vesicles (sEVs) and contribute to cancer progression. Here, we demonstrate that sEVs from PrCa patients show robust expression of both β1 integrins and c-Src. The impact of irradiation, a widely used therapy for the treatment of PrCa, on circulating sEVs is however not fully understood.
View Article and Find Full Text PDFJ Mol Histol
June 2025
Departament of Biological Sciences, Institute of Biosciences, Humanities and Exact Sciences, São Paulo State University (UNESP), São José do Rio Preto, São Paulo, Brazil.
The polyunsaturated fatty acid docosahexaenoic acid (DHA) has impressive anti-inflammatory and pro-resolution properties but its therapeutic use in PCa requires pre-clinical evidence. Here, the transgenic adenocarcinoma of the mouse prostate (TRAMP) was used as a pre-clinical model to assess the effect of DHA intake on the inflammatory microenvironment and proliferative and survival pathways in early- and late-stage disease. TRAMP mice were fed with standard rodent or DHA-enriched diet (DHA-d) for 4 (early stage) or 10 weeks (late stage).
View Article and Find Full Text PDFFront Immunol
June 2025
Departments of Medical Physics and Radiology, University of Wisconsin-Madison, Madison, WI, United States.
Background: Radiation therapy can modulate the tumor microenvironment (TME), influencing antitumor immune responses. This study compared the immunomodulatory effects of alpha-emitting (Ac) and beta-emitting (Lu) radiopharmaceutical therapies (RPT) using NM600 in murine prostate cancer models.
Methods: We assessed immunological changes in TRAMP-C1 and Myc-CaP tumor models treated with Ac-NM600 or Lu-NM600.
Viruses
May 2025
Department of Microbiology & Immunology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Both hepatitis B virus (HBV), an hepadnavirus with a DNA genome, and hepatitis A virus (HAV), a picornavirus, require the TRAMP-like host ZCCHC14-TENT4 complex for efficient replication. However, whereas HBV requires the nucleotidyltransferase activity of TENT4 to extend and stabilize the 3' poly(A) tails of mRNA transcribed from its genome, the role played by TENT4 in HAV replication is uncertain. HAV proteins are synthesized directly from its genomic RNA, which possesses a 3' poly(A) tail, with its length and composition presumably maintained by 3D-catalyzed RNA transcription during its replicative cycle.
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