Miller W H
Lady Davis Institute for Medical Research and SMBD Jewish General Hospital, Department of Oncology, McGill University, Montreal, Quebec, Canada.
Cancer. 1998 Oct 15;83(8):1471-82. doi: 10.1002/(sici)1097-0142(19981015)83:8<1471::aid-cncr1>3.0.co;2-6.
Although significant advances have been made in the treatment of some malignancies, the prognosis of patients with metastatic tumors remains poor. Differentiating agents redirect cells toward their normal phenotype and therefore may reverse or suppress evolving malignant lesions or prevent cancer invasion. In addition, they offer a potential alternative to the classic cytostatic drugs.
The purpose of this review was to examine the current and potential future roles of differentiating agents in the treatment of cancer.
Initial studies with differentiating agents focused on retinoid therapy. Although retinoids have shown some clinical success, their widespread use has been limited by resistance and, in the chemopreventive setting, toxicity. This has led to the synthesis of a number of new retinoids that currently are undergoing clinical investigation. A further approach to overcoming the drawbacks associated with exogenous retinoids has been to increase the levels of endogenous retinoic acid (RA) by inhibiting the cytochrome P450-mediated catabolism of RA using a novel class of agents known as retinoic acid metabolism blocking agents (RAMBAs). Liarozole, the first RAMBA to undergo clinical investigation, preferentially increases intratumor levels of endogenous RA resulting in antitumor activity.
Although studies using exogenous retinoids in this setting have not yet fulfilled their initial promise, studies with a growing set of synthetic retinoids are ongoing. Furthermore, modulation of endogenous retinoids may offer a significant new potential treatment for cancer.
尽管在某些恶性肿瘤的治疗方面已取得显著进展,但转移性肿瘤患者的预后仍然很差。分化剂可使细胞转向其正常表型,因此可能逆转或抑制正在发展的恶性病变或预防癌症侵袭。此外,它们为经典的细胞抑制药物提供了一种潜在的替代方案。
本综述的目的是研究分化剂在癌症治疗中的当前及潜在未来作用。
最初关于分化剂的研究集中在维甲酸治疗上。尽管维甲酸已显示出一些临床疗效,但其广泛应用受到耐药性的限制,并且在化学预防方面存在毒性。这导致了一些新型维甲酸的合成,目前这些新型维甲酸正在进行临床研究。克服外源性维甲酸相关缺点的另一种方法是通过使用一类称为维甲酸代谢阻断剂(RAMBAs)的新型药物抑制细胞色素P450介导的维甲酸分解代谢,从而提高内源性维甲酸(RA)的水平。利阿唑是首个进行临床研究的RAMBA,它优先提高肿瘤内源性RA的水平,从而产生抗肿瘤活性。
尽管在这种情况下使用外源性维甲酸的研究尚未实现其最初的承诺,但越来越多的合成维甲酸的研究正在进行。此外,调节内源性维甲酸可能为癌症提供一种重要的新的潜在治疗方法。