DNA fingerprinting techniques for the analysis of genetic and epigenetic alterations in colorectal cancer

被引:12
作者
Samuelsson, Johanna K. [1 ]
Alonso, Sergio [1 ]
Yamamoto, Fumiichiro [1 ]
Perucho, Manuel [1 ]
机构
[1] Sanford Burnham Med Res Inst SBMRI, La Jolla, CA 92037 USA
关键词
Colorectal cancer; DNA fingerprinting; Genetics; Epigenetics; COMPARATIVE GENOMIC HYBRIDIZATION; ABERRANT PROMOTER METHYLATION; FRAGMENT LENGTH POLYMORPHISM; CONSENSUS CODING SEQUENCES; POLYMERASE-CHAIN-REACTION; COPY-NUMBER CHANGES; COLON-CANCER; MICROSATELLITE INSTABILITY; LUNG-CANCER; GASTROINTESTINAL CANCER;
D O I
10.1016/j.mrfmmm.2010.08.010
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:61 / 76
页数:16
相关论文
共 156 条
[1]   CLUES TO THE PATHOGENESIS OF FAMILIAL COLORECTAL-CANCER [J].
AALTONEN, LA ;
PELTOMAKI, P ;
LEACH, FS ;
SISTONEN, P ;
PYLKKANEN, L ;
MECKLIN, JP ;
JARVINEN, H ;
POWELL, SM ;
JEN, J ;
HAMILTON, SR ;
PETERSEN, GM ;
KINZLER, KW ;
VOGELSTEIN, B ;
DELACHAPELLE, A .
SCIENCE, 1993, 260 (5109) :812-816
[2]  
Achille A, 1996, CANCER RES, V56, P3808
[3]  
Ahuja N, 1997, CANCER RES, V57, P3370
[4]  
Alberts B., 2002, The shape and structure of proteins, Vfourth, DOI 10.1093/aob/mcg023
[5]   Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene [J].
Albertson, DG ;
Ylstra, B ;
Segraves, R ;
Collins, C ;
Dairkee, SH ;
Kowbel, D ;
Kuo, WL ;
Gray, JW ;
Pinkel, D .
NATURE GENETICS, 2000, 25 (02) :144-146
[6]   Assessment of genomic damage in colorectal cancer by DNA fingerprinting: Prognostic applications [J].
Arribas, R ;
Capella, G ;
Tortola, S ;
Masramon, L ;
Grizzle, WE ;
Perucho, M ;
Peinado, MA .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (10) :3230-3240
[7]  
Asaga S, 2006, ANTICANCER RES, V26, P35
[8]   The random amplified polymorphic DNA (RAPD) assay and related techniques applied to genotoxicity and carcinogenesis studies: A critical review [J].
Atienzar, Franck A. ;
Jha, Awadhesh N. .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2006, 613 (2-3) :76-102
[9]   Isolation and characterization of a novel pituitary tumor apoptosis gene [J].
Bahar, A ;
Simpson, DJ ;
Cutty, SJ ;
Bicknell, JE ;
Hoban, PR ;
Holley, S ;
Mourtada-Maarbouni, M ;
Williams, GT ;
Clayton, RN ;
Farrell, WE .
MOLECULAR ENDOCRINOLOGY, 2004, 18 (07) :1827-1839
[10]   Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA [J].
Barrett, MT ;
Scheffer, A ;
Ben-Dor, A ;
Sampas, N ;
Lipson, D ;
Kincaid, R ;
Tsang, P ;
Curry, B ;
Baird, K ;
Meltzer, PS ;
Yakhini, Z ;
Bruhn, L ;
Laderman, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (51) :17765-17770