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新生小鼠中非交替多环芳烃的致瘤活性。

Tumorigenic activity of non-alternant polynuclear aromatic hydrocarbons in newborn mice.

作者信息

Lavoie E J, Braley J, Rice J E, Rivenson A

出版信息

Cancer Lett. 1987 Jan;34(1):15-20. doi: 10.1016/0304-3835(87)90068-1.

DOI:10.1016/0304-3835(87)90068-1
PMID:3802065
Abstract

The tumorigenic activity of benzo[b]fluoranthene, benzo[j]fluoranthene, benzo[k]fluoranthene, and indeno-[1,2,3-cd]pyrene was evaluated in newborn CD-1 mice. The total doses of these non-alternant polycyclic aromatic hydrocarbons employed in this study ranged from 0.5 to 2.1 mumol per mouse. The results of this assay indicate that both benzo[b]fluoranthene and benzo[j]fluoranthene exhibit significant tumorigenic activity. In contrast to these results, neither benzo[k]fluoranthene nor indeno[1,2,3-cd]pyrene were tumorigenic under these assay conditions.

摘要

在新生CD-1小鼠中评估了苯并[b]荧蒽、苯并[j]荧蒽、苯并[k]荧蒽和茚并[1,2,3-cd]芘的致瘤活性。本研究中使用的这些非交替多环芳烃的总剂量为每只小鼠0.5至2.1微摩尔。该试验结果表明,苯并[b]荧蒽和苯并[j]荧蒽均表现出显著的致瘤活性。与这些结果相反,在这些试验条件下,苯并[k]荧蒽和茚并[1,2,3-cd]芘均无致瘤性。

相似文献

1
Tumorigenic activity of non-alternant polynuclear aromatic hydrocarbons in newborn mice.新生小鼠中非交替多环芳烃的致瘤活性。
Cancer Lett. 1987 Jan;34(1):15-20. doi: 10.1016/0304-3835(87)90068-1.
2
Polycyclic aromatic hydrocarbons: 15 Listings - benz[a]anthracene, benzo[b]fluoranthene, benzo[j]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, dibenz[a,h]acridine, dibenz[a,j]acridine, dibenz[a,h]anthracene, 7H-dibenzo[c,g]carbazole, dibenzo[a,e]pyrene, dibenzo[a,h]pyrene, dibenzo[a,i]pyrene, dibenzo[a,l]pyrene, indeno[1,2,3-cd]pyrene, 5-methylchrysene.多环芳烃:15种物质——苯并[a]蒽、苯并[b]荧蒽、苯并[j]荧蒽、苯并[k]荧蒽、苯并[a]芘、二苯并[a,h]吖啶、二苯并[a,j]吖啶、二苯并[a,h]蒽、7H - 二苯并[c,g]咔唑、二苯并[a,e]芘、二苯并[a,h]芘、二苯并[a,i]芘、二苯并[a,l]芘、茚并[1,2,3 - cd]芘、5 - 甲基屈。
Rep Carcinog. 2011;12:353-61.
3
Mutagenicity and tumor initiating activity of methylated benzo[b]fluoranthenes.甲基化苯并[b]荧蒽的致突变性和肿瘤起始活性。
Carcinogenesis. 1985 Jul;6(7):1023-5. doi: 10.1093/carcin/6.7.1023.
4
Tumorigenic activity of the 4,5- and 9,10-dihydrodiols of benzo[j]fluoranthene and their syn- and anti-diol epoxides in newborn mice.苯并[j]荧蒽的4,5-二氢二醇和9,10-二氢二醇及其顺式和反式二醇环氧化物在新生小鼠中的致瘤活性。
Cancer Res. 1994 Feb 15;54(4):962-8.
5
Tumour initiating activity of dihydrodiols of benzo[b]fluoranthene, benzo[j]fluoranthene, and benzo[k]fluoranthene.苯并[b]荧蒽、苯并[j]荧蒽和苯并[k]荧蒽二氢二醇的肿瘤起始活性。
Carcinogenesis. 1982;3(1):49-52. doi: 10.1093/carcin/3.1.49.
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Exceptional tumor-initiating activity of 4-fluorobenzo[j]-fluoranthene on mouse skin: comparison with benzo[j]-fluoranthene, 10-fluoro-benzo[j]fluoranthene, benzo[a]pyrene, dibenzo[a,l]pyrene and 7,12-dimethylbenz[a]anthracene.4-氟苯并[j]荧蒽对小鼠皮肤的异常肿瘤起始活性:与苯并[j]荧蒽、10-氟苯并[j]荧蒽、苯并[a]芘、二苯并[a,l]芘和7,12-二甲基苯并[a]蒽的比较。
Cancer Lett. 1993 Jun 15;70(1-2):7-14. doi: 10.1016/0304-3835(93)90068-k.
7
Tumorigenicity in newborn mice of fjord region and other sterically hindered diol epoxides of benzo[g]chrysene, dibenzo[a,l]pyrene (dibenzo[def,p]chrysene), 4H-cyclopenta[def]chrysene and fluoranthene.峡湾地区苯并[g]屈、二苯并[a,l]芘(二苯并[def,p]屈)、4H-环戊二烯并[def]屈和荧蒽的空间位阻二醇环氧化物在新生小鼠中的致瘤性。
Carcinogenesis. 1995 Nov;16(11):2813-7. doi: 10.1093/carcin/16.11.2813.
8
Relative tumor initiating activity of benzo[a]fluoranthene, benzo[b]fluoranthene, naphtho[1,2-b]fluoranthene and naphtho[2,1-a]fluoranthene on mouse skin.苯并[a]荧蒽、苯并[b]荧蒽、萘并[1,2-b]荧蒽和萘并[2,1-a]荧蒽对小鼠皮肤的相对肿瘤起始活性。
Cancer Lett. 1990 Jul 31;52(3):229-33. doi: 10.1016/0304-3835(90)90191-y.
9
Tumorigenicity of nitrated derivatives of pyrene, benz[a]anthracene, chrysene and benzo[a]pyrene in the newborn mouse assay.芘、苯并[a]蒽、屈和苯并[a]芘的硝化衍生物在新生小鼠试验中的致瘤性。
Carcinogenesis. 1986 Aug;7(8):1317-22. doi: 10.1093/carcin/7.8.1317.
10
Fluoranthene and pyrene enhance benzo[a]pyrene--DNA adduct formation in vivo in mouse skin.荧蒽和芘可增强苯并[a]芘在小鼠皮肤体内形成DNA加合物的能力。
Cancer Lett. 1984 Oct;24(3):327-33. doi: 10.1016/0304-3835(84)90030-2.

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