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1
Organ-specific carcinogenicity of N-methyl-N-nitrosourea in F344 and ACI/N rats.N-甲基-N-亚硝基脲对F344和ACI/N大鼠的器官特异性致癌性。
J Cancer Res Clin Oncol. 1985;109(3):178-82. doi: 10.1007/BF00390353.
2
Carcinogenicity and organ specificity of N-trimethylsilylmethyl-N-nitrosourea (TMS-MNU), N-neopentyl-N-nitrosourea (neoPNU), and N-methyl-N-nitrosourea (MNU) in rats.N-三甲基硅烷基甲基-N-亚硝基脲(TMS-MNU)、N-新戊基-N-亚硝基脲(neoPNU)和N-甲基-N-亚硝基脲(MNU)对大鼠的致癌性和器官特异性
J Cancer Res Clin Oncol. 1988;114(5):473-6. doi: 10.1007/BF00391494.
3
DNA methylation in the digestive tract of F344 rats during chronic exposure to N-methyl-N-nitrosourea.F344大鼠长期暴露于N-甲基-N-亚硝基脲期间消化道中的DNA甲基化
J Cancer Res Clin Oncol. 1991;117(1):13-8. doi: 10.1007/BF01613190.
4
Induction of tumors in the small intestine and mammary gland of female Donryu rats by continuous oral administration of N-carboxymethyl-N-nitrosourea.通过持续口服N-羧甲基-N-亚硝基脲诱导雌性东京大鼠小肠和乳腺肿瘤
J Cancer Res Clin Oncol. 1983;106(1):12-6. doi: 10.1007/BF00399891.
5
Chemopreventive effects of zinc on prostate carcinogenesis induced by N-methyl-N-nitrosourea and testosterone in adult male Sprague-Dawley rats.锌对 N-甲基-N-亚硝脲和睾酮诱导的成年雄性 Sprague-Dawley 大鼠前列腺癌发生的化学预防作用。
J Cancer Res Clin Oncol. 2011 Apr;137(4):677-86. doi: 10.1007/s00432-010-0926-4. Epub 2010 Jun 16.
6
Experimental chemotherapy with N'N'-bis(2-chloroethyl)-N-nitrosourea (BCNU) in autochthonous neurogenic tumors of the rat transplacentally induced by ethylnitrosourea.用N'N'-双(2-氯乙基)-N-亚硝基脲(卡莫司汀)对经乙基亚硝基脲经胎盘诱导的大鼠自发性神经源性肿瘤进行实验性化疗。
J Cancer Res Clin Oncol. 1982;104(1-2):89-98. doi: 10.1007/BF00402057.
7
Two-year carcinogenicity study of 6-mercaptopurine in F344 rats.6-巯基嘌呤对F344大鼠的两年致癌性研究。
J Cancer Res Clin Oncol. 1990;116(3):245-50. doi: 10.1007/BF01612898.
8
Induction of lung tumors and peritoneal mesotheliomas in F344 rats given intragastric N-propyl-N-nitrosourea and histochemical, immunohistochemical, and ultrastructural characteristics of induced mesotheliomas.给F344大鼠灌胃N-丙基-N-亚硝基脲后诱发肺肿瘤和腹膜间皮瘤以及诱发间皮瘤的组织化学、免疫组织化学和超微结构特征
J Cancer Res Clin Oncol. 1988;114(3):259-65. doi: 10.1007/BF00405831.
9
Carcinogenesis in F-344 rats induced by nitrosohydroxyalkyl-chloroethylureas.亚硝基羟烷基 - 氯乙基脲诱发F - 344大鼠致癌作用。
J Cancer Res Clin Oncol. 1986;112(3):221-8. doi: 10.1007/BF00395916.
10
DNA strand breaks and death of thymocytes induced by N-methyl-N-nitrosourea.N-甲基-N-亚硝基脲诱导的DNA链断裂和胸腺细胞死亡。
J Cancer Res Clin Oncol. 1992;118(1):23-9. doi: 10.1007/BF01192307.

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1
Evaluation of a 4-day repeated-dose micronucleus test in rat glandular stomach and colon using aneugens and non-genotoxic non-carcinogens.使用非整倍体诱导剂和非遗传毒性非致癌物对大鼠腺胃和结肠进行为期4天的重复剂量微核试验评估。
Genes Environ. 2022 Apr 11;44(1):12. doi: 10.1186/s41021-022-00241-6.
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Antioxidant and immunity activities of Fufang Kushen Injection Liquid.复方苦参注射液的抗氧化及免疫活性。
Molecules. 2012 May 30;17(6):6481-90. doi: 10.3390/molecules17066481.
3
Effects of X-irradiation on N-methyl-N-nitrosourea-induced multi-organ carcinogenesis in rats.X射线辐射对N-甲基-N-亚硝基脲诱导的大鼠多器官致癌作用的影响。
Jpn J Cancer Res. 1993 Jan;84(1):26-33. doi: 10.1111/j.1349-7006.1993.tb02779.x.
4
Lack of any positive effect of intestinal metaplasia on induction of gastric tumors in Wistar rats treated with N-methyl-N-nitrosourea in their drinking water.在用含N-甲基-N-亚硝基脲的饮用水处理的Wistar大鼠中,肠化生对胃肿瘤诱导无任何积极作用。
Jpn J Cancer Res. 1994 Sep;85(9):892-6. doi: 10.1111/j.1349-7006.1994.tb02965.x.
5
Elevated serum growth hormone accelerates gastric tumorigenesis in F344 rats after treatment with N-methyl-N-nitrosourea in their drinking water.在F344大鼠饮用含N-甲基-N-亚硝基脲的水后,血清生长激素升高会加速胃肿瘤发生。
Jpn J Cancer Res. 1995 Jul;86(7):631-7. doi: 10.1111/j.1349-7006.1995.tb02445.x.
6
Experimental induction of ovarian Sertoli cell tumors in rats by N-nitrosoureas.用N-亚硝基脲在大鼠中实验诱导卵巢支持细胞瘤
Environ Health Perspect. 1987 Aug;73:115-23. doi: 10.1289/ehp.8773115.
7
Carcinogenicity and organ specificity of N-trimethylsilylmethyl-N-nitrosourea (TMS-MNU), N-neopentyl-N-nitrosourea (neoPNU), and N-methyl-N-nitrosourea (MNU) in rats.N-三甲基硅烷基甲基-N-亚硝基脲(TMS-MNU)、N-新戊基-N-亚硝基脲(neoPNU)和N-甲基-N-亚硝基脲(MNU)对大鼠的致癌性和器官特异性
J Cancer Res Clin Oncol. 1988;114(5):473-6. doi: 10.1007/BF00391494.
8
DNA methylation in the digestive tract of F344 rats during chronic exposure to N-methyl-N-nitrosourea.F344大鼠长期暴露于N-甲基-N-亚硝基脲期间消化道中的DNA甲基化
J Cancer Res Clin Oncol. 1991;117(1):13-8. doi: 10.1007/BF01613190.
9
Modifying effects of various chemicals on preneoplastic and neoplastic lesion development in a wide-spectrum organ carcinogenesis model using F344 rats.在使用F344大鼠的广谱器官致癌模型中,各种化学物质对癌前和肿瘤性病变发展的修饰作用。
Jpn J Cancer Res. 1991 Jun;82(6):642-9. doi: 10.1111/j.1349-7006.1991.tb01899.x.
10
Enhancing potential of 6 different carcinogens on multi-organ tumorigenesis after initial treatment with N-methyl-N-nitrosourea in rats.在大鼠经N-甲基-N-亚硝基脲初始处理后,增强6种不同致癌物对多器官肿瘤发生的影响。
Jpn J Cancer Res. 1991 Dec;82(12):1397-405. doi: 10.1111/j.1349-7006.1991.tb01812.x.

本文引用的文献

1
Induction of duodenal-tumors and thymomas in Fischer rats by continuous oral administration of 1-propyl-1-nitrosourea.通过持续口服1-丙基-1-亚硝基脲诱导Fischer大鼠十二指肠肿瘤和胸腺瘤。
Gan. 1980 Apr;71(2):231-7.
2
Induction of duodenal tumors in F344 rats by continuous oral administration of N-ethyl-N-nitrosourea.
J Natl Cancer Inst. 1980 Mar;64(3):613-6.
3
Induction of tumors in the small intestine and mammary gland of female Donryu rats by continuous oral administration of N-carboxymethyl-N-nitrosourea.通过持续口服N-羧甲基-N-亚硝基脲诱导雌性东京大鼠小肠和乳腺肿瘤
J Cancer Res Clin Oncol. 1983;106(1):12-6. doi: 10.1007/BF00399891.
4
Spontaneous tumors in F-344/DuCrj rats.F-344/DuCrj大鼠的自发性肿瘤。
Gan. 1983 Jun;74(3):365-72.
5
Carcinogenicity of N-nitroso compounds. Species and route differences in regard to organotropism.N-亚硝基化合物的致癌性。关于器官嗜性的物种和途径差异。
Oncology. 1980;37(4):237-42. doi: 10.1159/000225444.
6
Carcinogenicity of low doses of N-ethyl-N-nitrosourea in F344 rats; a dose-response study.
Gan. 1984 Feb;75(2):117-25.
7
Induction of digestive-tract tumors in F344 rats by continuous oral administration of N-butyl-N-nitrosourea.通过连续口服N-丁基-N-亚硝基脲诱导F344大鼠消化道肿瘤
J Cancer Res Clin Oncol. 1984;107(1):32-7. doi: 10.1007/BF00395487.
8
Spontaneous tumors of the nervous system and associated organs and/or tissues in rats.大鼠神经系统及相关器官和/或组织的自发性肿瘤
Gan. 1984 Sep;75(9):784-91.
9
Leukemogenesis of N-nitrosobutylurea in the rat. I. Effect of various concentrations in the drinking water to female Donryu rats.N-亚硝基丁脲对大鼠的白血病诱导作用。I. 饮用水中不同浓度对雌性东京大鼠的影响。
Gan. 1970 Jun;61(3):245-53.
10
Spontaneous tumors in ACI/N rats.ACI/N大鼠的自发性肿瘤。
J Natl Cancer Inst. 1975 Dec;55(6):1437-45. doi: 10.1093/jnci/55.6.1437.

N-甲基-N-亚硝基脲对F344和ACI/N大鼠的器官特异性致癌性。

Organ-specific carcinogenicity of N-methyl-N-nitrosourea in F344 and ACI/N rats.

作者信息

Maekawa A, Matsuoka C, Onodera H, Tanigawa H, Furuta K, Ogiu T, Mitsumori K, Hayashi Y

出版信息

J Cancer Res Clin Oncol. 1985;109(3):178-82. doi: 10.1007/BF00390353.

DOI:10.1007/BF00390353
PMID:4008511
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12253545/
Abstract

Male and female F344 rats were continuously administered N-methyl-N-nitrosourea (MNU) in their drinking water at concentrations of 200 or 100 ppm, and both sexes of ACI/N rats were given MNU at a concentration of 200 ppm. By the 42nd week of the experiment, high incidences of brain/spinal cord tumors were observed in both strains of rats. Histologically, many of them were astrocytomas or anaplastic astrocytomas. In addition, malignant neurinomas were also detected in the spinal nerve roots and trigeminal nerves, although their incidences were rather low. There was no difference in the type and incidence of these neurogenic tumors between the two strains of rats. Tumors of the tongue and esophagus were mainly observed in the high-dose group of F344 rats and those of the glandular stomach were observed in the low-dose group of F344 rats. In ACI/N rats, tumors of the heart and renal pelvis were detected. The organ-specific carcinogenicity of MNU in these two strains of rats was compared with that of MNU in Donryu rats. It was demonstrated that organ specificity of MNU given orally was influenced not only by the strain of rats but also by the dose level.

摘要

将雄性和雌性F344大鼠的饮用水中持续加入浓度为200或100 ppm的N-甲基-N-亚硝基脲(MNU),并给ACI/N大鼠两性给予浓度为200 ppm的MNU。到实验第42周时,在两种品系的大鼠中均观察到脑/脊髓肿瘤的高发生率。组织学上,其中许多是星形细胞瘤或间变性星形细胞瘤。此外,在脊神经根和三叉神经中也检测到恶性神经鞘瘤,尽管其发生率相当低。两种品系大鼠之间这些神经源性肿瘤的类型和发生率没有差异。舌和食管肿瘤主要在高剂量组的F344大鼠中观察到,而腺胃肿瘤在低剂量组的F344大鼠中观察到。在ACI/N大鼠中,检测到心脏和肾盂肿瘤。将MNU在这两种品系大鼠中的器官特异性致癌性与MNU在唐育大鼠中的进行比较。结果表明,口服MNU的器官特异性不仅受大鼠品系影响,还受剂量水平影响。