Møllersen Linda, Paulsen Jan Erik, Alexander Jan
Department of Food Toxicology, Division of Environmental Medicine, Norwegian Institute of Public Health, Oslo, Norway.
Anticancer Res. 2004 Sep-Oct;24(5A):2595-9.
C57BL/6J Min/+ mice, which carry a nonsense mutation in Apc, were injected twice neonatally with 5 mg azoxymethane (AOM) /kg body weight. AOM treatment in comparison with untreated Min mice increased the incidence and number of colonic tumours from 6/14 to 22/24 (incidence) and 0.64+/-0.9 to 4.0+/-3.5 tumours per mice, respectively. Colonic tumours were analysed for loss of heterozygosity (LOH) in Apc, and 32 of the samples showed LOH whereas 14 did not. In untreated Min mice, all 8 tumours had LOH in Apc. All tumour samples from the AOM-treated Min mice were analysed for nonsense mutations between codons 686 and 1217 in the Apc gene, and one sample had a G-->A transition mutation in codon 1047. No beta-catenin mutations in the region coding for phosphorylation sites important for degradation were found. In conclusion, the main mechanism for colonic tumour induction in AOM-induced Min mice is LOH in Apc, but Apc nonsense mutations may also occur.
携带Apc基因无义突变的C57BL/6J Min/+小鼠在新生期接受两次腹腔注射,剂量为5mg/kg体重的氧化偶氮甲烷(AOM)。与未处理的Min小鼠相比,AOM处理使结肠肿瘤的发生率和数量分别从6/14增加到22/24(发生率),每只小鼠的肿瘤数量从0.64±0.9增加到4.0±3.5。分析结肠肿瘤中Apc基因杂合性缺失(LOH)情况,32个样本显示有LOH,14个样本没有。在未处理的Min小鼠中,所有8个肿瘤在Apc基因中都有LOH。对AOM处理的Min小鼠的所有肿瘤样本分析Apc基因第686至1217密码子之间的无义突变,一个样本在密码子1047处有G→A转换突变。在对降解重要的磷酸化位点编码区域未发现β-连环蛋白突变。总之,AOM诱导的Min小鼠结肠肿瘤发生的主要机制是Apc基因的LOH,但也可能发生Apc无义突变。