Crespo-Ortiz Maria P, Wei Ming Q
Department of Biomedical Science, Faculty of Basic and Health Science, Santiago de Cali University, Pampalinda Campus, Cali, Colombia.
J Biomed Biotechnol. 2012;2012:247597. doi: 10.1155/2012/247597. Epub 2011 Nov 22.
Improvement of quality of life and survival of cancer patients will be greatly enhanced by the development of highly effective drugs to selectively kill malignant cells. Artemisinin and its analogs are naturally occurring antimalarials which have shown potent anticancer activity. In primary cancer cultures and cell lines, their antitumor actions were by inhibiting cancer proliferation, metastasis, and angiogenesis. In xenograft models, exposure to artemisinins substantially reduces tumor volume and progression. However, the rationale for the use of artemisinins in anticancer therapy must be addressed by a greater understanding of the underlying mechanisms involved in their cytotoxic effects. The primary targets for artemisinin and the chemical base for its preferential effects on heterologous tumor cells need yet to be elucidated. The aim of this paper is to provide an overview of the recent advances and new development of this class of drugs as potential anticancer agents.
开发能够选择性杀死恶性细胞的高效药物将极大地提高癌症患者的生活质量和生存率。青蒿素及其类似物是天然存在的抗疟药物,已显示出强大的抗癌活性。在原发性癌症培养物和细胞系中,它们的抗肿瘤作用是通过抑制癌症增殖、转移和血管生成来实现的。在异种移植模型中,接触青蒿素可显著减小肿瘤体积并延缓肿瘤进展。然而,必须通过更深入地了解其细胞毒性作用的潜在机制来阐明青蒿素用于抗癌治疗的基本原理。青蒿素的主要靶点及其对异源肿瘤细胞产生优先作用的化学基础仍有待阐明。本文的目的是概述这类药物作为潜在抗癌剂的最新进展和新发展。