Leslie Amy, Pratt Norman R, Gillespie Karen, Sales Mark, Kernohan Neil M, Smith Gillian, Wolf C Roland, Carey Francis A, Steele Robert J C
Department of Surgery and Molecular Oncology, University of Dundee, Ninewells Hospital, Dundee DD1 9SY, Scotland, UK.
Cancer Res. 2003 Aug 1;63(15):4656-61.
It is widely accepted that both large-scale chromosomal abnormalities and mutation of specific genes, such as APC, K-ras, and/or p53, occur in the majority of colorectal adenocarcinomas. Whether or not a relationship exists between these different forms of genetic abnormalities was previously unknown. Using comparative genomic hybridization and mutational analysis of APC, K-ras, and p53 to evaluate 50 colorectal adenocarcinomas, we have shown that mutation of p53 is significantly associated with gain of 20q, 13q, and 8q and loss of 18q (P = 0.000, 0.02, 0.044, and 0.001, respectively). Conversely, APC mutation did not associate with any of the above-mentioned aberrations but did associate significantly with gain of 7p (P = 0.01). Gain of chromosomal arm 12p, although a less common aberration, was significantly associated with K-ras mutation (P = 0.011). The associations we have described should refine the search for candidate genes underlying chromosomal aberrations and assist in the definition of distinct pathways in colorectal tumorigenesis.
人们普遍认为,大多数结直肠癌中都会出现大规模染色体异常以及特定基因(如APC、K-ras和/或p53)的突变。此前尚不清楚这些不同形式的基因异常之间是否存在关联。通过使用比较基因组杂交以及对APC、K-ras和p53进行突变分析来评估50例结直肠癌,我们发现p53突变与20q、13q和8q的增加以及18q的缺失显著相关(P值分别为0.000、0.02、0.044和0.001)。相反,APC突变与上述任何一种畸变均无关联,但与7p的增加显著相关(P = 0.01)。染色体臂12p的增加虽然是一种不太常见的畸变,但与K-ras突变显著相关(P = 0.011)。我们所描述的这些关联应能优化对染色体畸变潜在候选基因的寻找,并有助于明确结直肠癌发生的不同途径。