[1]
|
De Bont, R. and van Larebeke, N. (2004) Endogenous DNA damage in humans: A review of quantitative data. Mutagenesis, 19, 169-185. doi:10.1093/mutage/geh025
|
[2]
|
Lindahl, T. (1993) Instability and decay of the primary structure of DNA. Nature, 362, 709-715.
doi:10.1038/362709a0
|
[3]
|
Jackson, A.L. and Loeb, L.A. (2001) The contribution of endogenous sources of DNA damage to the multiple mutations in cancer. Mutation Research, 477, 7-21.
doi:10.1016/S0027-5107(01)00091-4
|
[4]
|
Nohmi, T., Kim, S.R. and Yamada, M. (2005) Modulation of oxidative mutagenesis and carcinogenesis by polymorphic forms of human DNA repair enzymes. Mutation Research, 591, 60-73.
doi:10.1016/j.mrfmmm.2005.03.033
|
[5]
|
Ohno, M., et al. (2006) A genome-wide distribution of 8- oxoguanine correlates with the preferred regions for recombination and single nucleotide polymorphism in the human genome. Genome Research, 16, 567-575.
doi:10.1101/gr.4769606
|
[6]
|
Slupska, M.M., et al. (1999) Functional expression of hMYH, a human homolog of the Escherichia coli MutY protein. Journal of Bacteriology, 181, 6210-6213.
|
[7]
|
Ohtsubo, T., et al. (2000) Identification of human MutY homolog (hMYH) as a repair enzyme for 2-hydro-xyadenine in DNA and detection of multiple forms of hMYH located in nuclei and mitochondria. Nucleic Acids Research, 28, 1355-1364. doi:10.1093/nar/28.6.1355
|
[8]
|
Shinmura, K., et al. (2000) Adenine excisional repair function of MYH protein on the adenine: 8-hydroxy-guanine base pair in double-stranded DNA. Nucleic Acids Research, 28, 4912-4918. doi:10.1093/nar/28.24.4912
|
[9]
|
Tsuzuki, T., Nakatsu, Y. and Nakabeppu, Y. (2007) Significance of error-avoiding mechanisms for oxidative DNA damage in carcinogenesis. Cancer Science, 98, 465-470.
doi:10.1111/j.1349-7006.2007.00409.x
|
[10]
|
Michaels, M.L., et al. (1992) Evidence that MutY and MutM combine to prevent mutations by an oxidatively damaged form of guanine in DNA. Proceedings of the National Academy of Sciences of the USA, 89, 7022-7025.
doi:10.1073/pnas.89.15.7022
|
[11]
|
Charames, G.S. and Bapat, B. (2003) Genomic instability and cancer. Current Molecular Medicine, 3, 589-596.
doi:10.2174/1566524033479456
|
[12]
|
Al-Tassan, N., et al., Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors. Nature Genetics, 30, 227-232. doi:10.1038/ng828
|
[13]
|
Cheadle, J.P. and Sampson, J.R. (2007) MUTYH-associated polyposis from defect in base excision repair to clinical genetic testing. DNA Repair, 6, 274-279.
doi:10.1016/j.dnarep.2006.11.001
|
[14]
|
Enholm, S., et al. (2003) Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients. American Journal of Pathology, 163, 827-832.
doi:10.1016/S0002-9440(10)63443-8
|
[15]
|
Halford, S.E., et al. (2003) Germline mutations but not somatic changes at the MYH locus contribute to the pathogenesis of unselected colorectal cancers. American Journal of Pathology, 162, 1545-1548.
doi:10.1016/S0002-9440(10)64288-5
|
[16]
|
Jones, S., et al. (2002) Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C-->T:A mutations. Human Molecular Genetics, 11, 2961-2967. doi:10.1093/hmg/11.23.2961
|
[17]
|
Sampson, J.R., et al. (2003) Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH. Lancet, 362, 39-41.
doi:10.1016/S0140-6736(03)13805-6
|
[18]
|
Sieber, O.M., et al. (2003) Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH. The New England Journal of Medicine, 348, 791-799. doi:10.1056/NEJMoa025283
|
[19]
|
Kambara, T., et al (2004) Role of inherited defects of MYH in the development of sporadic colorectal cancer. Genes Chromosomes Cancer, 40, 1-9.
doi:10.1002/gcc.20011
|
[20]
|
Yamaguchi, S., et al. (2002) A single nucleotide polymorphism at the splice donor site of the human MYH base excision repair genes results in reduced translation efficiency of its transcripts. Genes Cells, 7, 461-474.
doi:10.1046/j.1365-2443.2002.00532.x
|
[21]
|
Miyaki, M., et al. (2005) Germline mutations of the MYH gene in Japanese patients with multiple colorectal adenomas. Mutation Research, 578, 430-433.
doi:10.1016/j.mrfmmm.2005.01.017
|
[22]
|
Tao, H., et al. (2008) Association between genetic polymerphisms of the base excision repair gene MUTYH and increased colorectal cancer risk in a Japanese population. Cancer Science, 99, 355-360.
doi:10.1111/j.1349-7006.2007.00694.x
|
[23]
|
Parker, A.R. and Eshleman, J.R. (2003) Human MutY: Gene structure, protein functions and interactions, and role in carcinogenesis. Cellular and Molecular Life Sciences, 60, 2064-2083. doi:10.1007/s00018-003-3053-4
|
[24]
|
Nielsen, M., et al. (2007) Cost-utility analysis of genetic screening in families of patients with germline MUTYH mutations. BMC Medical Genetics, 8, 42.
doi:10.1186/1471-2350-8-42
|
[25]
|
Rahman, N. and Scott, R.H. (2007) Cancer genes associated with phenotypes in monoallelic and biallelic mutation carriers: new lessons from old players. Human Molecular Genetics, 16, 60-66. doi:10.1093/hmg/ddm026
|
[26]
|
Sulova, M., et al. (2007) Mutation analysis of the MYH gene in unrelated Czech APC mutation-negative polyposis patients. European Journal of Cancer, 43, 1617- 1621. doi:10.1016/j.ejca.2007.04.010
|
[27]
|
Shields, P.G. and Harris, C.C. (2000) Cancer risk and low-penetrance susceptibility genes in gene-environment interactions. Journal of Clinical Oncology, 18, 2309- 2315.
|
[28]
|
Peterlongo, P., et al. (2005) Colorectal cancer risk in individuals with biallelic or monoallelic mutations of MYH. International Journal of Cancer, 114, 505-507.
doi:10.1002/ijc.20767
|
[29]
|
Boiteux, S. and Radicella, J.P. (2000) The human OGG1 gene: structure, functions, and its implication in the process of carcinogenesis. Archives of Biochemistry and Biophysics, 377, 1-8. doi:10.1006/abbi.2000.1773
|
[30]
|
Nakabeppu, Y., et al. (2004) The defense mechanisms in mammalian cells against oxidative damage in nucleic acids and their involvement in the suppression of mutagenesis and cell death. Free Radical Research, 38, 423- 429. doi:10.1080/10715760410001688348
|
[31]
|
Bruner, S.D., Norman, D.P. and Verdine, G.L. (2000) Structural basis for recognition and repair of the endogenous mutagen 8-oxoguanine in DNA. Nature, 403, 859- 866. doi:10.1038/35002510
|
[32]
|
Shinmura, K. and Yokota, J. (2001) The OGG1 gene encodes a repair enzyme for oxidatively damaged DNA and is involved in human carcinogenesis. Antioxidants and Redox Signaling, 3, 597-609.
doi:10.1089/15230860152542952
|
[33]
|
Croitoru, M.E., et al. (2004) Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk. Journal of the National Cancer Institute, 96, 1631-1634. doi:10.1093/jnci/djh288
|
[34]
|
Fleischmann, C., et al. (2004) Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer. International Journal of Cancer, 109, 554-558. doi:10.1002/ijc.20020
|
[35]
|
Kairupan, C.F., et al. (2005) Mutation analysis of the MYH gene in an Australian series of colorectal polyposis patients with or without germline APC mutations. International Journal of Cancer, 116, 73-77.
doi:10.1002/ijc.20983
|
[36]
|
Tao, H., et al. (2004) A novel splicesite variant of the base excision repair gene MYH is associated with production of an aberrant mRNA transcript encoding a truncated MYH protein not localized in the nucleus. Carcinogenesis, 25, 1859-1866. doi:10.1093/carcin/bgh206
|
[37]
|
Zhang, Y., et al. (2006) Germline mutations and polymorphic variants in MMR, E-cadherin and MYH genes associated with familial gastric cancer in Jiangsu of China. International Journal of Cancer, 119, 2592-2596.
doi:10.1002/ijc.22206
|
[38]
|
Kim, I.J., et al. (2004) Mutational analysis of OGG1, MYH, MTH1 in FAP, HNPCC and sporadic colorectal cancer patients: R154H OGG1 polymorphism is associated with sporadic colorectal cancer patients. Human Genetics, 115, 498-503. doi:10.1007/s00439-004-1186-7
|
[39]
|
Huang, M., et al. (2007) High-order interactions among genetic variants in DNA base excision repair pathway genes and smoking in bladder cancer susceptibility. Cancer Epidemiology, Biomarkers and Prevention, 16, 84-91.
doi:10.1158/1055-9965.EPI-06-0712
|
[40]
|
Miyaishi, A., et al. (2009) MUTYH Gln324His gene polymerphism and genetic susceptibility for lung cancer in a Japanese population. Journal of Experimental and Clinical Cancer Research, 28, 10.
doi:10.1186/1756-9966-28-10
|