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黄酮8-乙酸:我们目前对其在实体瘤中作用机制的理解

Flavone 8-acetic acid: our current understanding of its mechanism of action in solid tumours.

作者信息

Cummings J, Smyth J F

机构信息

Imperial Cancer Research Fund Medical Oncology Unit, Western General Hospital, Edinburgh, United Kingdom.

出版信息

Cancer Chemother Pharmacol. 1989;24(5):269-72. doi: 10.1007/BF00304756.

Abstract

Flavone 8-acetic acid (FAA) represents a novel chemical structure undergoing clinical trials as an anticancer drug. Its unusual properties tend to distinguish it from a conventional cytotoxic compound, particularly in the response of solid murine tumours; as a consequence, novel mechanisms of action are currently under investigation. In this review we summarised these mechanisms into one of the three categories (a) direct cytotoxicity, (b) biologic response modifier and (c) pharmacologic effector and considered the evidence for and against each. FAA is cytotoxic to tumour cells in vitro, but only at high concentrations and after long exposures. In vivo it is considerably more cytotoxic to the same cells, and it is unlikely that direct cytotoxicity alone can account for this difference. FAA stimulates NK cell activity, induces interferon alpha and synergises with interleukin 2 in the treatment of murine renal cancer. However, a definite link between immunomodulation and antitumour activity has still to be confirmed. Perhaps FAA's most unusual property is its ability to reduce tumour blood flow dramatically, which may provide the appropriate conditions for reactive chemistry to occur. Finally, a combination of the above mechanisms probably work together in producing the drug's unique spectrum of antitumour activity.

摘要

黄酮8 - 乙酸(FAA)是一种正处于临床试验阶段的新型抗癌化学结构药物。其独特性质使其有别于传统细胞毒性化合物,尤其是在对实体小鼠肿瘤的反应方面;因此,目前正在研究其新的作用机制。在本综述中,我们将这些机制归纳为以下三类之一:(a)直接细胞毒性,(b)生物反应调节剂,(c)药理效应剂,并考量了支持和反对每一类机制的证据。FAA在体外对肿瘤细胞具有细胞毒性,但仅在高浓度和长时间暴露后才会出现这种情况。在体内,它对相同细胞的细胞毒性要大得多,仅靠直接细胞毒性不太可能解释这种差异。FAA可刺激自然杀伤细胞活性、诱导α干扰素,并在治疗小鼠肾癌时与白细胞介素2协同作用。然而,免疫调节与抗肿瘤活性之间的明确联系仍有待证实。或许FAA最不同寻常的特性是其能显著减少肿瘤血流,这可能为发生反应性化学作用提供适宜条件。最后,上述多种机制可能共同作用,产生该药物独特的抗肿瘤活性谱。

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