Moon R C, McCormick D L, Mehta R G
Cancer Res. 1983 May;43(5 Suppl):2469s-2475s.
Retinoids are effective inhibitors of chemical carcinogenesis in the mammary gland and urinary bladder of experimental animals. Modification of the basic retinoid structure has produced retinoids with increased target organ specificity, resulting in increased anticancer activity with reduced systemic toxicity. Combining retinoid treatment with hormonal manipulation results in a synergistic inhibition of mammary carcinogenesis; this combination approach also inhibits development of additional mammary cancers following surgical removal of the first mammary cancer. Retinoids are most effective when administered shortly after the carcinogenic insult. However, even when retinoid treatment is delayed, the compounds are still effective cancer chemopreventive agents for the mammary gland and urinary bladder. The length of time that retinoid exposure can be delayed and retain an anticancer effect is directly related to tumor latency, with a longer delay permissible against tumors with long latent periods.
维甲酸是实验动物乳腺和膀胱化学致癌作用的有效抑制剂。对基本维甲酸结构的修饰产生了具有更高靶器官特异性的维甲酸,从而在降低全身毒性的同时提高了抗癌活性。将维甲酸治疗与激素调控相结合可协同抑制乳腺癌发生;这种联合方法还能抑制在手术切除首例乳腺癌后其他乳腺癌的发展。维甲酸在致癌损伤后不久给药时最为有效。然而,即使维甲酸治疗延迟,这些化合物仍是乳腺和膀胱有效的癌症化学预防剂。维甲酸暴露可延迟并保持抗癌效果的时间长度与肿瘤潜伏期直接相关,对于潜伏期长的肿瘤允许更长的延迟时间。