Histoprotective and antiproliferative effects of Raloxifene treatment during prostate carcinogenesis in rats
Recommended Citation
Pinho CF, Soares L, Chamelete JLG, Salata GC, Aquino AM, Freitas A, Pereira S, Mendes LO, Scarano WR. Histoprotective and Antiproliferative Effects of Raloxifene Treatment During Prostate Carcinogenesis in Rats. Toxicol Appl Pharmacol. 2026;515:117947.
Document Type
Article
Publication Date
10-1-2026
Publication Title
Toxicology and applied pharmacology
Keywords
Animals, Male, Raloxifene Hydrochloride, Cell Proliferation, Rats, Inbred F344, Prostatic Neoplasms, Methylnitrosourea, Rats, Prostate, Selective Estrogen Receptor Modulators, Carcinogenesis
Abstract
The ability of prostate cancer to progress to castration-resistant disease underscores the importance of study on adjuvant therapies. Recent research suggests estrogen receptors as possible therapeutic targets in neoplasias and they can be modulated by drugs such as Raloxifene. In this context, this study aimed to evaluate the effects of Raloxifene therapy during prostatic carcinogenesis through exposure to the carcinogen N-methyl-N-nitrosourea (MNU). To this end, male Fisher 344 rats underwent a tumor induction protocol using MNU (15 mg/kg), followed or not by treatment with Raloxifene (10 mg/kg). Raloxifene mitigated the tissue alterations induced by the tumor induction protocol by attenuating cell proliferation and the development of lesions, and by limiting their progression to malignancy. Additionally, the periacinar smooth muscle layer and the stromal distribution of collagen fibers were preserved in Raloxifene group. These results pointed to a protective role of Raloxifene on the prostatic microenvironment, attenuating the structural and proliferative alterations that accumulate during the carcinogenic process.
Medical Subject Headings
Animals; Male; Raloxifene Hydrochloride; Cell Proliferation; Rats, Inbred F344; Prostatic Neoplasms; Methylnitrosourea; Rats; Prostate; Selective Estrogen Receptor Modulators; Carcinogenesis
PubMed ID
42447936
Volume
515
First Page
117947
Last Page
117947
