Watanabe H, Shimokado K, Asahara T, Dohi K, Niwa O
Second Department of Surgery, Hiroshima University School of Medicine.
Jpn J Cancer Res. 1999 Jan;90(1):40-7. doi: 10.1111/j.1349-7006.1999.tb00663.x.
We have examined 63 methylcholanthrene (MCA)-induced mouse sarcomas for possible correlations of mutations involving the c-myc, ras and p53 genes. The c-myc gene was found to be amplified in 18 of these sarcomas (29%). Polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) analysis and subsequent direct sequencing identified 18 cases carrying K-ras mutation at codons 12, 13 and 61 (29%). No mutation was detected in the H-ras and N-ras genes. Mutations of the p53 gene in exons 5 to 8 were found in 45 cases (71%). Comparison of these mutations revealed that out of 18 cases with c-myc gene amplifications, 10 carried K-ras mutations (56%) and 14 carried p53 mutations (78%). In contrast, among 45 cases of sarcomas without c-myc gene amplification, 8 were found to have K-ras mutations (18%). The same 45 cases were found to have 31 p53 mutations (69%). The present study suggests a strong correlation between c-myc gene amplification and K-ras gene mutation (P < 0.01). p53 gene mutation was frequently found among MCA-induced mouse sarcomas, indicating the importance of this mutation in the etiology of these tumors. However, p53 mutations were present in sarcomas regardless of the state of c-myc amplification and K-ras mutation. Therefore, a defect in the p53 gene is independent of amplification of the c-myc gene or point mutation of the K-ras gene.
我们检测了63个甲基胆蒽(MCA)诱导的小鼠肉瘤,以寻找涉及c-myc、ras和p53基因的突变之间可能存在的相关性。在这些肉瘤中,有18个(29%)发现c-myc基因发生扩增。聚合酶链反应-单链构象多态性(PCR-SSCP)分析及随后的直接测序确定了18个病例在密码子12、13和61处携带K-ras突变(29%)。在H-ras和N-ras基因中未检测到突变。在外显子5至8中发现p53基因的突变有45例(71%)。对这些突变的比较显示,在18例c-myc基因扩增的病例中,10例携带K-ras突变(56%),14例携带p53突变(78%)。相比之下,在45例无c-myc基因扩增的肉瘤病例中,发现8例有K-ras突变(18%)。同样的45例病例中有31例p53突变(69%)。本研究表明c-myc基因扩增与K-ras基因突变之间存在很强的相关性(P < 0.01)。p53基因突变在MCA诱导的小鼠肉瘤中很常见,表明该突变在这些肿瘤的病因学中具有重要意义。然而,无论c-myc扩增状态和K-ras突变情况如何,p53突变都存在于肉瘤中。因此,p53基因缺陷独立于c-myc基因扩增或K-ras基因点突变。