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2003 - 2004年海洋药理学:抗肿瘤及细胞毒性化合物

Marine pharmacology in 2003-2004: anti-tumour and cytotoxic compounds.

作者信息

Mayer Alejandro M S, Gustafson Kirk R

机构信息

Department of Pharmacology, Chicago College of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.

出版信息

Eur J Cancer. 2006 Sep;42(14):2241-70. doi: 10.1016/j.ejca.2006.05.019. Epub 2006 Aug 9.

DOI:10.1016/j.ejca.2006.05.019
PMID:16901686
Abstract

During 2003 and 2004, marine pharmacology research directed towards the discovery and development of novel anti-tumour agents was published in 163 peer-reviewed articles. The purpose of this review is to present a structured assessment of the anti-tumour and cytotoxic properties of 150 marine natural products, many of which are novel compounds that belong to diverse structural classes, including polyketides, terpenes, steroids and peptides. The organisms yielding these bioactive marine compounds include invertebrate animals, algae, fungi and bacteria. Anti-tumour pharmacological studies were conducted with 31 structurally defined marine natural products in a number of experimental and clinical models that further defined their mechanisms of action. Particularly potent in vitro cytotoxicity data generated with murine and human tumour cell lines was reported for 119 novel marine chemicals with as yet undetermined mechanisms of action. Noteworthy is the fact that marine anti-cancer research was sustained by a global collaborative effort, involving researchers from Australia, Austria, Canada, China, Egypt, France, Germany, Italy, Japan, Mexico, the Netherlands, New Zealand, Papua New Guinea, the Philippines, South Africa, South Korea, Spain, Switzerland, Taiwan, Thailand and the United States of America (USA). Finally, this 2003-2004 overview of the marine pharmacology literature highlights the fact that the discovery of novel marine anti-tumour agents continued at the same pace as during 1998-2002.

摘要

在2003年至2004年期间,有关新型抗肿瘤药物发现与开发的海洋药理学研究发表在163篇经过同行评审的文章中。本综述的目的是对150种海洋天然产物的抗肿瘤和细胞毒性特性进行结构化评估,其中许多是属于不同结构类别的新型化合物,包括聚酮化合物、萜类、甾体和肽类。产生这些具有生物活性的海洋化合物的生物包括无脊椎动物、藻类、真菌和细菌。对31种结构明确的海洋天然产物在一些实验和临床模型中进行了抗肿瘤药理学研究,进一步明确了它们的作用机制。报道了119种作用机制尚未确定的新型海洋化学物质对小鼠和人类肿瘤细胞系产生的特别有效的体外细胞毒性数据。值得注意的是,海洋抗癌研究是由全球合作努力维持的,参与的研究人员来自澳大利亚、奥地利、加拿大、中国、埃及、法国、德国、意大利、日本、墨西哥、荷兰、新西兰、巴布亚新几内亚、菲律宾、南非、韩国、西班牙、瑞士、台湾、泰国和美利坚合众国(美国)。最后,这份2003 - 2004年海洋药理学文献综述突出了这样一个事实,即新型海洋抗肿瘤药物的发现与1998 - 2002年期间保持相同的速度。

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