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Somatic mutation in the mammary gland: influence of time and estrus.

机译:乳腺体细胞突变:时间和发情的影响。

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摘要

A critical factor in the quantitation of mutation induction in vivo is the time interval between treatment and sampling. In order to study mutagenesis in the mammary epithelium, the cell type in which breast cancer arises, we have measured the manifestation time, the minimum time required for the maximum mutant frequency to be achieved, in this tissue. The F1 LacZ transgenic mice (Muta MousexSWR) were treated with N-ethyl-N-nitrosourea (ENU) at 50 mg/kg for five consecutive days and then sampled at 1, 2, 4, 6, 9, or 12 weeks after the last treatment. The LacZ- mutant frequency reached a maximum at 4 weeks post-treatment and did not vary significantly thereafter. Dlb-1- mutations in the small intestine reached a maximum at 2 weeks after treatment and did not vary significantly thereafter. Since the stage of estrus cycle during carcinogen exposure influences the mammary tumor incidence and latency, it was expected that it would also affect mutation induction. To test this, F1 LacZ mice in the estrus or di-estrus stage were treated with an acute dose of 250 mg/kg ENU and sampled 10-13 weeks post-treatment. No statistical difference between the two groups was found, indicating that the effect of estrus on carcinogenesis is not due to variation in the sensitivity of the stage of the mammary gland to mutation. Copyright 1999 Elsevier Science B.V.
机译:体内突变诱导定量的关键因素是治疗和采样之间的时间间隔。为了研究乳腺上皮(发生乳腺癌的细胞类型)中的诱变,我们测量了该组织中的表现时间,即达到最大突变频率所需的最短时间。 F1 LacZ转基因小鼠(Muta MousexSWR)用N-乙基-N-亚硝基脲(ENU)以50 mg / kg的剂量连续处理五天,然后在第1、2、4、6、9或12周取样最后的治疗。 LacZ突变体频率在治疗后4周达到最大值,此后没有明显变化。小肠中的Dlb-1-突变在治疗后2周达到最大,此后没有明显变化。由于致癌物暴露期间的发情周期阶段会影响乳腺肿瘤的发生率和潜伏期,因此预计也会影响突变诱导。为了对此进行测试,对发情或发情期的F1 LacZ小鼠进行了250 mg / kg ENU的急性剂量治疗,并在治疗后10-13周取样。两组之间未发现统计学差异,这表明发情对癌变的影响并非归因于乳腺突变阶段敏感性的变化。版权所有1999 Elsevier Science B.V.

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