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首页> 外文期刊>Cancer biology & therapy >Enhanced acute apoptotic response to azoxymethane-induced DNA damage in the rodent colonic epithelium by Tyrian purple precursors: a potential colorectal cancer chemopreventative.
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Enhanced acute apoptotic response to azoxymethane-induced DNA damage in the rodent colonic epithelium by Tyrian purple precursors: a potential colorectal cancer chemopreventative.

机译:Tyrian紫色前体对啮齿动物结肠上皮中由乙氧基甲烷诱导的DNA损伤的急性凋亡反应增强:一种潜在的结直肠癌化学预防剂。

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Colorectal cancer (CRC) is the second most prevalent and deadly cancer worldwide. Due to the mortality and morbidity associated with chemotherapeutic regimes, research is turning to natural product enhancement of the acute apoptotic response to genotoxic carcinogens (AARGC). Although Tyrian purple dye pigments and precursors from muricid molluscs are known for their anti-proliferative and proapoptotic activity, the chemoprotective properties of these edible molluscs has not been assessed. Enhancement of AARGC by oral administration of muricid extract (ME), containing a mixture of the cytotoxins tyrindoleninone and 6-bromoisatin, was assessed in an azoxymethane (AOM) rodent model. A dose-dependent increase in apoptotic index was observed in the distal colon, with a significant increase detected at an ME dose of 1.0 mg/g (p < 0.01). Proliferation (PCNA) index failed to vary significantly at this ME concentration, which confirms the ME-induced increase in apoptotic response to DNA alkylation. ME also appears to confer no major toxic side effects, as all mice consistently gained weight during the trial and colonic crypt height was maintained (p > 0.05) independent of ME dose. Although, this is the first example of AARGC enhancement by indole-based compounds, bioactive precursor degradation in simulated gastric fluid may prevent introduction of muricids as a chemopreventative food. Nevertheless, the protective effect of ME against CRC in vivo clearly substantiates further research into the chemopreventative efficacy of Muricidae natural products.
机译:大肠癌(CRC)是全球第二大最致命的癌症。由于与化学疗法有关的死亡率和发病率,研究转向天然产物增强对遗传毒性致癌物(AARGC)的急性凋亡反应。尽管泰里安紫色染料颜料和鼠类软体动物的前体以其抗增殖和促凋亡活性而著称,但尚未评估这些食用软体动物的化学保护性能。在乙氧基甲烷(AOM)啮齿动物模型中评估了通过口服施用含有细胞毒素酪氨酸多烯酮和6-溴异丁香素混合物的鼠科提取物(ME)来增强AARGC的效果。在远端结肠中观察到凋亡指数的剂量依赖性增加,在1.0 mg / g的ME剂量下,凋亡指数显着增加(p <0.01)。在此ME浓度下,增殖(PCNA)指数没有显着变化,这证实了ME诱导的对DNA烷基化的凋亡反应增加。 ME似乎也没有带来重大的毒副作用,因为所有小鼠在试验期间持续增加体重,并且结肠隐窝高度得以维持(p> 0.05),与ME剂量无关。尽管这是基于吲哚的化合物增强AARGC的第一个例子,但是在模拟胃液中生物活性前体的降解可能会阻止引入杀鼠剂作为化学预防食品。然而,ME对CRC在体内的保护作用显然证实了对Muricidae天然产物化学预防功效的进一步研究。

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