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α-二氟甲基鸟氨酸对用N-甲基-N'-硝基-N-亚硝基胍处理的大鼠胃肿瘤发生的抑制作用。

Inhibition of gastric tumorigenesis by alpha-difluoromethylornithine in rats treated with N-methyl-N'-nitro-N-nitrosoguanidine.

作者信息

Lehnert T, Buhl K, Ivankovic S

机构信息

Department of Surgery, University of Heidelberg, Germany.

出版信息

J Cancer Res Clin Oncol. 1993;119(10):594-8. doi: 10.1007/BF01372722.

Abstract

Male Wistar rats were treated concurrently with a combination of the carcinogen N-methyl-N'-nitro-N-nitrosoguanidine (MNNG; CAS 70-25-7) and the polyamine-synthesis inhibitor alpha-difluoromethylornithine (DFMO) at two different doses of 0.5% and 1.0% (w/v). Experimental groups were treated with (I) MNNG alone (n = 25), (II) MNNG plus 0.5% (w/v) DFMO (n = 25), (III) MNNG plus 1.0% (w/v) DFMO (n = 25), (IV) 1.0% (w/v) DFMO alone (n = 25). Group V represented untreated controls (n = 20). Both the carcinogen and DFMO were administered in drinking water. The treatment time with the carcinogen and DFMO was 35 weeks. After treatment was completed animals were followed for an additional 50 weeks to cover a total observation time of 85 weeks. Significantly fewer animals developed gastric adenocarcinoma in the two groups of animals that received a combined treatment of MNNG plus DFMO compared to animals treated with the carcinogen alone (P < 0.05 and 0.005). No benign or malignant neoplastic lesions were observed in the stomach or duodenum of animals treated with DFMO alone or in untreated controls. It is concluded that concurrent treatment with DFMO prevents the development of malignant gastric epithelial tumors induced by MNNG in rats.

摘要

将雄性Wistar大鼠同时用致癌物N-甲基-N'-硝基-N-亚硝基胍(MNNG;化学物质登录号70-25-7)和多胺合成抑制剂α-二氟甲基鸟氨酸(DFMO)以0.5%和1.0%(w/v)两种不同剂量进行处理。实验组分别接受以下处理:(I)单独使用MNNG(n = 25),(II)MNNG加0.5%(w/v)DFMO(n = 25),(III)MNNG加1.0%(w/v)DFMO(n = 25),(IV)单独使用1.0%(w/v)DFMO(n = 25)。第五组为未处理的对照组(n = 20)。致癌物和DFMO均通过饮用水给予。致癌物和DFMO的处理时间为35周。处理完成后,对动物再随访50周,以使总观察时间达到85周。与单独用致癌物处理的动物相比,接受MNNG加DFMO联合处理的两组动物中发生胃腺癌的动物明显较少(P < 0.05和0.005)。在单独用DFMO处理的动物或未处理的对照组动物的胃或十二指肠中未观察到良性或恶性肿瘤性病变。结论是,DFMO联合处理可预防MNNG诱导的大鼠恶性胃上皮肿瘤的发生。

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