Ana R Gomes, Elisiário J Tavares-da-Silva, Fernanda M F Roleira, Ana S Pires
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引用次数: 0
摘要
胰腺癌仍然是世界上最危及生命的癌症之一,治疗选择有限,预后差。尽管治疗方案取得了进展,但胰腺癌患者的死亡率仍在继续上升,这证明需要新的治疗药物。甾体衍生物以其独特的可修饰框架,在药物发现,即寻找新的抗癌药物方面,已成为一类有前途的化合物。本文综述了合成甾体衍生物和天然甾体衍生物在胰腺癌治疗中的抗癌活性,重点介绍了它们的结构通用性、作用机制和最新进展。为此,在两个主要数据库PubMed和Web of Science中进行了广泛的文献检索。在临床前环境中,本综述中描述的甾体衍生物通过不同的机制显示其细胞毒性,其最终导致细胞凋亡。值得注意的是,受这类化合物影响的许多途径被认为是许多癌症特征的关键参与者,这加强了研究类固醇衍生物治疗胰腺癌的重要性。本文综述了甾体衍生物的研究现状,强调了其作为胰腺癌治疗新方法基础的潜力,并概述了其作为有效抗癌药物的未来发展方向。
Steroidal derivatives in pancreatic cancer: Paving the way to new anticancer drugs.
Pancreatic cancer remains one of the most life-threatening cancers worldwide with limited therapeutic options and a poor prognosis. Despite the advances in treatment regimens, the death rate of pancreatic cancer patients continues to rise, justifying the need for novel therapeutic agents. Steroidal derivatives, with their unique modifiable framework, have emerged as a promising class of compounds in drug discovery, namely for the search for novel anticancer drugs. A comprehensive review of studies on the anticancer activity of synthetic and natural steroidal derivatives for potential pancreatic cancer treatment was conducted, highlighting their structural versatility, mechanisms of action, and recent advances in their development. For this, an extensive literature search was conducted in two main databases - PubMed and Web of Science. In the preclinical setting, the steroidal derivatives described throughout this review display their cytotoxicity by different mechanisms, which culminate in cell death mostly by apoptosis. Remarkably, many of the pathways affected by this class of compounds are considered key players in many of the hallmarks of cancer, which reinforces the importance of studying steroidal derivatives for the treatment of pancreatic cancer. This review summarises the current state of research and underscores the potential of steroidal derivatives as a groundwork for novel therapeutic approaches in pancreatic cancer management, outlining future directions for their development as effective anticancer agents.