Sanford-Burnham Medical Research Institute (SBMRI), 10901N. Torrey Pines Rd, La Jolla, CA 92037, United States.
Mutat Res. 2010 Nov 10;693(1-2):61-76. doi: 10.1016/j.mrfmmm.2010.08.010. Epub 2010 Sep 17.
Genetic somatic alterations are fundamental hallmarks of cancer. In addition to point and other small mutations targeting cancer genes, solid tumors often exhibit aneuploidy as well as multiple chromosomal rearrangements of large fragments of the genome. Whether somatic chromosomal alterations and aneuploidy are a driving force or a mere consequence of tumorigenesis remains controversial. Recently it became apparent that not only genetic but also epigenetic alterations play a major role in carcinogenesis. Epigenetic regulation mechanisms underlie the maintenance of cell identity crucial for development and differentiation. These epigenetic regulatory mechanisms have been found substantially altered during cancer development and progression. In this review, we discuss approaches designed to analyze genetic and epigenetic alterations in colorectal cancer, especially DNA fingerprinting approaches to detect changes in DNA copy number and methylation. DNA fingerprinting techniques, despite their modest throughput, played a pivotal role in significant discoveries in the molecular basis of colorectal cancer. The aim of this review is to revisit the fingerprinting technologies employed and the oncogenic processes that they unveiled.
遗传体细胞改变是癌症的基本特征。除了针对癌症基因的点突变和其他小突变外,实体瘤还经常表现出非整倍体以及基因组大片段的多种染色体重排。体细胞染色体改变和非整倍体是肿瘤发生的驱动因素还是仅仅是后果仍存在争议。最近,人们明显意识到,不仅遗传改变,而且表观遗传改变在癌症发生中也起着主要作用。表观遗传调控机制是维持细胞特性所必需的,这些特性对于发育和分化至关重要。在癌症的发生和发展过程中,这些表观遗传调控机制发生了实质性改变。在这篇综述中,我们讨论了用于分析结直肠癌中遗传和表观遗传改变的方法,特别是用于检测 DNA 拷贝数和甲基化变化的 DNA 指纹分析方法。尽管 DNA 指纹分析技术的通量较低,但在揭示结直肠癌分子基础的重大发现中发挥了关键作用。本综述的目的是重新审视所采用的指纹分析技术以及揭示的致癌过程。