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N-甲基-N'-亚硝基脲在器官培养中对小鼠乳腺上皮细胞的肿瘤转化及DNA损伤作用

Neoplastic transformation and DNA damage of mouse mammary epithelial cells by N-methyl-N'-nitrosourea in organ culture.

作者信息

Delp C R, Treves J S, Banerjee M R

机构信息

Tumor Biology Laboratory, School of Biological Sciences, University of Nebraska-Lincoln 68588-0342.

出版信息

Cancer Lett. 1990 Nov 19;55(1):31-7. doi: 10.1016/0304-3835(90)90062-3.

Abstract

An appropriate in vitro system was used to study the effect of a direct-acting carcinogen on the transformation of mammary epithelial cells in the organ culture of the whole mammary gland in vitro. Studies were done to determine the ability of N-methyl-N'-nitrosourea (MNU) to transform the mammary cells in organ culture. Mouse mammary glands were treated with single or multiple doses of MNU during various periods of the culture. To assay for neoplastic transformation potential of MNU on mammary cells, mammary glands were dissociated and the cells were injected into the parenchyma-free inguinal mammary fat pad of syngeneic virgin female host mice. Palpable tumors were observed in injected glands of 23% of the mice after 3-4 months and an additional 31% showed serially transplantable hyperplastic alveolar nodules (HANs). Histopathologic examination of the tissues showed that the tumors were mammary adenocarcinoma. All tumors and hyperplasias were secondarily transplanted into syngeneic animals, resulting in tumors and hyperplasias of similar histopathology. In addition, DNA damage of the epithelial cells in organ culture caused by MNU was also measurable using the new nick translation assay. The most extensive DNA damage occurred when the glands were treated on day 4 and day 5 of the mammogenic culture period. These results demonstrate that the mouse mammary epithelial cells are susceptible to the carcinogenic action of the direct-acting carcinogen MNU and that the whole mammary gland-culture system offers an appropriate in vitro model for studying the mechanism of carcinogenesis induced by MNU.

摘要

采用合适的体外系统,研究一种直接作用致癌物对全乳腺器官体外培养中乳腺上皮细胞转化的影响。开展研究以确定N-甲基-N'-亚硝基脲(MNU)在器官培养中转化乳腺细胞的能力。在培养的不同时期,用单剂量或多剂量的MNU处理小鼠乳腺。为了测定MNU对乳腺细胞的肿瘤转化潜能,将乳腺解离,然后将细胞注射到同基因处女雌性宿主小鼠无实质的腹股沟乳腺脂肪垫中。3 - 4个月后,在23%的小鼠注射腺体中观察到可触及的肿瘤,另外31%表现出可连续移植的增生性肺泡结节(HANs)。对组织进行组织病理学检查显示,肿瘤为乳腺腺癌。所有肿瘤和增生均再次移植到同基因动物体内,导致组织病理学相似的肿瘤和增生。此外,使用新的缺口平移分析也可检测到MNU在器官培养中引起的上皮细胞DNA损伤。在生乳培养期的第4天和第5天处理腺体时,DNA损伤最为广泛。这些结果表明,小鼠乳腺上皮细胞对直接作用致癌物MNU的致癌作用敏感,并且全乳腺培养系统为研究MNU诱导的致癌机制提供了合适的体外模型。

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