吡非尼酮和维生素D在实验性动物模型中靶向心脏和肾脏纤维化通路的研究

S. Antar, M. El-Azab, Reem M Hazem, M. Saleh
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引用次数: 2

摘要

乳腺癌被认为是女性中最常见的癌症,在埃及占38.8%,在世界占29%。它是女性癌症相关死亡的第二大常见原因。用阿霉素治疗乳腺癌可能会导致许多副作用,主要是心脏和肾脏纤维化。本研究旨在探讨吡非尼酮(500mg/kg,每日1次口服)和维生素D (0.5μg/kg每日1次口服)对阿霉素(15mg /kg口服)诱导的心脏和肾脏纤维化的潜在抗纤维化作用的潜在分子机制。此外,将在乳腺癌异种移植实验模型中评估吡非尼酮(PFD)和维生素D单独使用或与阿霉素联合使用的抗癌潜力。然后在治疗两周后采集组织和血液样本,评估阿霉素的毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigating Pirfenidone and Vitamin D for Targeting Cardiac and Renal Fibrotic Pathways in Experimentally-Induced Animal Model
Breast cancer is considered as the most familiar cancer in females which represented 38.8 % in Egypt and 29% in the world. It is the second common cause of cancer-related death in women. Treatment of breast cancer with Doxorubicin may lead to many side effects, mainly cardiac and renal fibrosis. The present study aimed to investigate the underlying molecular mechanisms for the potential anti-fibrotic effect of pirfenidone (500mg/kg, P.O. once daily) and Vitamin D (0.5μg/kg I.P. once daily) against doxorubicin (15 mg/kg I.P.) induced cardioand renalfibrosis. Moreover, the anti-cancer potential of pirfenidone (PFD) and Vitamin D either alone or in combination with doxorubicin will be assessed in a xenograft experimental model of breast cancer. Then, tissue and blood samples will be collected after two weeks posttreatment to assess the toxicity of Doxorubicin.
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