|
1
|
Fengju S, Guanglin W and Kexin C:
Incidence of colon cancer in Tianjin, China, 1981ߝ2000. Asia Pac J
Public Health. 17:22–25. 2005. View Article : Google Scholar : PubMed/NCBI
|
|
2
|
de la Chapelle A: Genetic predisposition
to colorectal cancer. Nat Rev Cancer. 4:769–780. 2004. View Article : Google Scholar : PubMed/NCBI
|
|
3
|
Kunkel TA and Erie DA: DNA mismatch
repair. Annu Rev Biochem. 74:681–710. 2005. View Article : Google Scholar : PubMed/NCBI
|
|
4
|
Lipkin SM, Rozek LS, Rennert G, Yang W,
Chen PC, Hacia J, Hunt N, Shin B, Fodor S, Kokoris M, et al: The
MLH1 D132H variant is associated with susceptibility to sporadic
colorectal cancer. Nat Genet. 36:694–699. 2004. View Article : Google Scholar : PubMed/NCBI
|
|
5
|
Fearnhead NS, Wilding JL, Winney B, Tonks
S, Bartlett S, Bicknell DC, Tomlinson IP, Mortensen NJ and Bodmer
WF: Multiple rare variants in different genes account for
multifactorial inherited susceptibility to colorectal adenomas.
Proc Natl Acad Sci USA. 101:15992–15997. 2004. View Article : Google Scholar : PubMed/NCBI
|
|
6
|
Tomlinson IP, Webb E, Carvajal-Carmona L,
Broderick P, Howarth K, Pittman AM, Spain S, Lubbe S, Walther A,
Sullivan K, et al: A genome-wide association study identifies
colorectal cancer susceptibility loci on chromosomes 10p14 and
8q23.3. Nat Genet. 40:623–630. 2008. View
Article : Google Scholar : PubMed/NCBI
|
|
7
|
Christmann M, Tomicic MT, Roos WP and
Kaina B: Mechanisms of human DNA repair: An update. Toxicology.
193:3–34. 2003. View Article : Google Scholar : PubMed/NCBI
|
|
8
|
Lynch HT and de la Chapelle A: Hereditary
colorectal cancer. N Engl J Med. 348:919–932. 2003. View Article : Google Scholar : PubMed/NCBI
|
|
9
|
Hampel H, Frankel WL, Martin E, Arnold M,
Khanduja K, Kuebler P, Nakagawa H, Sotamaa K, Prior TW, Westman J,
et al: Screening for the Lynch syndrome (hereditary nonpolyposis
colorectal cancer). N Engl J Med. 352:1851–1860. 2005. View Article : Google Scholar : PubMed/NCBI
|
|
10
|
Ito E, Yanagisawa Y, Iwahashi Y, Suzuki Y,
Nagasaki H, Akiyama Y, Sugano S, Yuasa Y and Maruyama K: A core
promoter and a frequent single-nucleotide polymorphism of the
mismatch repair gene hMLH1. Biochem Biophys Res Commun.
256:488–494. 1999. View Article : Google Scholar : PubMed/NCBI
|
|
11
|
Arita M, Zhong X, Min Z, Hemmi H and
Shimatake H: Multiple sites required for expression in 5′-flanking
region of the hMLH1 gene. Gene. 306:57–65. 2003. View Article : Google Scholar : PubMed/NCBI
|
|
12
|
Simpkins SB, Bocker T, Swisher EM, Mutch
DG, Gersell DJ, Kovatich AJ, Palazzo JP, Fishel R and Goodfellow
PJ: MLH1 promoter methylation and gene silencing is the primary
cause of microsatellite instability in sporadic endometrial
cancers. Hum Mol Genet. 8:661–666. 1999. View Article : Google Scholar : PubMed/NCBI
|
|
13
|
Zou XP, Dai WJ and Cao J: CDH1 promoter
polymorphism (−347G->GA) is a possible prognostic factor in
sporadic colorectal cancer. World J Gastroenterol. 15:5340–5345.
2009. View Article : Google Scholar : PubMed/NCBI
|
|
14
|
Mei Q, Yan HL, Ding FX, Xue G, Huang JJ,
Wang YZ and Sun SH: Single-nucleotide polymorphisms of mismatch
repair genes in healthy Chinese individuals and sporadic colorectal
cancer patients. Cancer Genet Cytogenet. 171:17–23. 2006.
View Article : Google Scholar : PubMed/NCBI
|
|
15
|
Campbell PT, Curtin K, Ulrich CM, Samowitz
WS, Bigler J, Velicer CM, Caan B, Potter JD and Slattery ML:
Mismatch repair polymorphisms and risk of colon cancer, tumour
microsatellite instability and interactions with lifestyle factors.
Gut. 58:661–667. 2009. View Article : Google Scholar : PubMed/NCBI
|
|
16
|
Park SH, Lee GY, Jeon HS, Lee SJ, Kim KM,
Jang SS, Kim CH, Lee WK, Kam S, Park RW, et al: -93G->A
polymorphism of hMLH1 and risk of primary lung cancer. Int J
Cancer. 112:678–682. 2004. View Article : Google Scholar : PubMed/NCBI
|
|
17
|
Lo YL, Hsiao CF, Jou YS, Chang GC, Tsai
YH, Su WC, Chen KY, Chen YM, Huang MS, Hsieh WS, et al:
Polymorphisms of MLH1 and MSH2 genes and the risk of lung cancer
among never smokers. Lung Cancer. 72:280–286. 2011. View Article : Google Scholar : PubMed/NCBI
|
|
18
|
Allan JM, Shorto J, Adlard J, Bury J,
Coggins R, George R, Katory M, Quirke P, Richman S, Scott D, et al:
MLH1-93G>A promoter polymorphism and risk of mismatch repair
deficient colorectal cancer. Int J Cancer. 123:2456–2459. 2008.
View Article : Google Scholar : PubMed/NCBI
|
|
19
|
Raptis S, Mrkonjic M, Green RC, Pethe VV,
Monga N, Chan YM, Daftary D, Dicks E, Younghusband BH, Parfrey PS,
et al: MLH1-93G>A promoter polymorphism and the risk of
microsatellite-unstable colorectal cancer. J Natl Cancer Inst.
99:463–474. 2007. View Article : Google Scholar : PubMed/NCBI
|
|
20
|
Chen H, Taylor NP, Sotamaa KM, Mutch DG,
Powell MA, Schmidt AP, Feng S, Hampel HL, de la Chapelle A and
Goodfellow PJ: Evidence for heritable predisposition to epigenetic
silencing of MLH1. Int J Cancer. 120:1684–1688. 2007. View Article : Google Scholar : PubMed/NCBI
|
|
21
|
Brenner C, Deplus R, Didelot C, Loriot A,
Viré E, De Smet C, Gutierrez A, Danovi D, Bernard D, Boon T, et al:
Myc represses transcription through recruitment of DNA
methyltransferase corepressor. EMBO J. 24:336–346. 2005. View Article : Google Scholar : PubMed/NCBI
|
|
22
|
Brenner C and Fuks F: DNA
methyltransferases: Facts, clues, mysteries. Curr Top Microbiol
Immunol. 301:45–66. 2006.PubMed/NCBI
|
