Masramon L, Arribas R, Tórtola S, Perucho M, Peinado M A
Institut de Recerca Oncològica (Department of Cancer and Metastasis), Hospital Duran i Reynals, Barcelona, Spain.
Br J Cancer. 1998 Jun;77(12):2349-56. doi: 10.1038/bjc.1998.390.
C-myc gene activation is a common event in multiple types of neoplasia and has been associated with different cellular processes relevant to the malignant transformation of cancer cells. C-myc gene amplification has been analysed in colorectal carcinomas by means of an innovative DNA fingerprinting method based on the arbitrarily primed PCR. This method requires a low amount of DNA, uses multiple internal controls and appears sensitive and reproducible. Clinicopathological and molecular correlates have been investigated in a series of 70 colorectal carcinomas. The incidence of c-myc amplification was 26%, ranging from two- to fivefold increase in copy number. C-myc amplification occurrence was more frequent in more advanced stages of tumour invasion (P < 0.001) and was associated with mutations in the p53 tumour-suppressor gene (P = 0.048). The presence of c-myc amplification was indicative of a shorter disease-free survival period but, because of its strong association with Dukes' stage, its prognostic value is questionable.
C-myc基因激活是多种肿瘤形成中的常见事件,并且与癌细胞恶性转化相关的不同细胞过程有关。已通过基于任意引物PCR的创新DNA指纹图谱方法分析了结直肠癌中的C-myc基因扩增。该方法需要少量DNA,使用多个内部对照,并且似乎灵敏且可重复。在一系列70例结直肠癌中研究了临床病理和分子相关性。c-myc扩增的发生率为26%,拷贝数增加2至5倍。c-myc扩增在肿瘤浸润的更晚期阶段更频繁发生(P < 0.001),并且与p53肿瘤抑制基因突变相关(P = 0.048)。c-myc扩增的存在表明无病生存期较短,但是由于其与Dukes分期密切相关,其预后价值存在疑问。