Anzano M A, Smith J M, Uskoković M R, Peer C W, Mullen L T, Letterio J J, Welsh M C, Shrader M W, Logsdon D L, Driver C L
Laboratory of Chemoprevention, National Cancer Institute, Bethesda, Maryland 20892.
Cancer Res. 1994 Apr 1;54(7):1653-6.
We have used the vitamin D analogue, 1 alpha,25-dihydroxy-16-ene-23-yne-26,27-hexafluorocholecalcifero l (Ro24-5531), for inhibition of mammary carcinogenesis induced by N-nitroso-N-methylurea (NMU) in Sprague-Dawley rats. Rats were first treated with a single dose of either 15 or 50 mg/kg body weight NMU and then fed Ro24-5531 (2.5 or 1.25 nmol/kg of diet) for 5-7 months. Ro24-5531 significantly extended tumor latency and lessened tumor incidence as well as tumor number in rats treated with the lower dose of NMU. In rats treated with the higher dose of NMU, Ro24-5531 was fed in combination with tamoxifen; in these experiments, Ro24-5531 significantly enhanced the ability of tamoxifen to reduce total tumor burden, as well as to increase the probability that an animal would be tumor free at the end of the experiment. In vitro, Ro24-5531 was 10-100 times more potent than 1,25-dihydroxyvitamin D3 for inhibition of proliferation of human breast cancer cell lines as well as primary cultures of cells from 2 patients with acute myelogenous leukemia. When fed chronically, Ro24-5531 did not elevate serum calcium in the present studies. We propose the new term, "deltanoids," for the set of molecules composed of vitamin D and its synthetic analogues, in a manner similar to the naming of "retinoids" for the corresponding set of molecules related to vitamin A.
我们使用了维生素D类似物1α,25 - 二羟基 - 16 - 烯 - 23 - 炔 - 26,27 - 六氟胆钙化醇(Ro24 - 5531),来抑制N - 亚硝基 - N - 甲基脲(NMU)诱导的Sprague - Dawley大鼠的乳腺癌变。大鼠首先接受15或50mg/kg体重的NMU单剂量处理,然后喂食Ro24 - 5531(2.5或1.25nmol/kg饲料)5 - 7个月。Ro24 - 5531显著延长了低剂量NMU处理大鼠的肿瘤潜伏期,降低了肿瘤发生率以及肿瘤数量。在高剂量NMU处理的大鼠中,Ro24 - 5531与他莫昔芬联合喂食;在这些实验中,Ro24 - 5531显著增强了他莫昔芬降低总肿瘤负荷的能力,以及增加了实验结束时动物无肿瘤的概率。在体外,Ro24 - 5531抑制人乳腺癌细胞系以及2例急性髓性白血病患者细胞原代培养物增殖的能力比1,25 - 二羟基维生素D3强10 - 100倍。在本研究中,长期喂食Ro24 - 5531并未升高血清钙。我们以类似于将与维生素A相关的相应分子组命名为“类视黄醇”的方式,为维生素D及其合成类似物组成的分子组提出了新术语“δ类化合物”。