以紫杉烷为基础的化疗药物联合治疗前列腺癌:新见解和未来方向

BioChem Pub Date : 2023-08-29 DOI:10.3390/biochem3030009
Rafaella S. Coelho, S. M. Rocha, Cláudio J. Maia
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引用次数: 0

摘要

肿瘤疾病是一个重大的全球健康问题,每年造成数千人死亡,并对患者的生活质量产生重大影响。前列腺癌(PCa)是西方世界男性癌症相关死亡的第二大诊断癌症和第四大原因。描述PCa发展过程中的发病途径和关键驱动分子改变为预测疾病结果和确定潜在治疗靶点的生物标志物评估提供了路线图。从20世纪90年代开始引入的化疗药物包括紫杉醇(紫杉醇、多西紫杉醇和卡巴他赛),它们是最常用于前列腺癌治疗的抗癌药物。本文综述了目前关于前列腺癌的发病和发展的知识,紫杉烷为基础的治疗的最新进展,以及它们与针对不同跨膜癌蛋白的前列腺癌联合治疗的进展。一些跨膜蛋白的沉默可以提高紫杉烷的敏感性,因此可能是提高这些药物在PCa治疗中的有效性的一种机制。这种联合疗法需要作为一种潜在的治疗药物来减少前列腺癌的细胞增殖、迁移和侵袭性。
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Combined Therapies with Taxane-Based Chemotherapeutic Drugs in Prostate Cancer: Novel Insights and Future Directions
Oncologic disease is a significant global health issue that causes thousands of deaths annually, and it has a significant impact on the quality of life of patients. Prostate cancer (PCa) is the second most diagnosed cancer and the fourth leading cause of cancer-related death in men in the Western world. Delineation of pathogenetic pathways and key driver molecular alterations involved in PCa development has provided a roadmap for the evaluation of biomarkers in predicting disease outcome and to identify potential therapeutic targets. Chemotherapeutic agents introduced from the 1990s include the taxanes (paclitaxel, docetaxel, and cabazitaxel), which are the anticancer drugs used most frequently for PCa treatment. This review presents the current knowledge about the onset and development of PCa, the state of the art of the use of taxane-based therapy, and their combination with targeting different transmembrane oncoproteins in PCa. The silencing of some transmembrane proteins can improve taxane sensitivity, and therefore may be a mechanism to improve the effectiveness of these drugs in PCa treatment. This combined therapy needs to be explored as a potential therapeutic agent for reducing cell proliferation, migration, and invasiveness in PCa.
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