Interaction of Exo1 genotypes and smoking habit in oral cancer in Taiwan

Oral Oncology

Volumn 45, Issue 9, 2009, Pages

  Tsai, Ming Hsui ^a   Tseng, Hsien Chang ^a   Liu, Chiu Shong ^a   Chang, Chia Lin ^a   Tsai, Chia Wen ^a,b   Tsou, Yung An ^a   Wang, Rou Fen ^a   Lin, Cheng Chieh ^a   Wang, Hwei Chung ^a   Chiu, Chang Fang ^a   Bau, Da Tian ^a,b  

^a CHINA MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

^b CHINA MEDICAL UNIVERSITY   (Taiwan)

Author keywords

Carcinogenesis; Exo1; Oral cancer; Polymorphism

Indexed keywords

EXONUCLEASE;

ADULT; ALLELE; ARTICLE; CANCER RISK; CONTROL GROUP; ENVIRONMENTAL FACTOR; FEMALE; GENDER; GENE FREQUENCY; GENOTYPE; HOSPITAL; HUMAN; MAJOR CLINICAL STUDY; MALE; MOUTH CANCER; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SMOKING; TAIWAN;

AGED; ALLELES; CASE-CONTROL STUDIES; EXODEOXYRIBONUCLEASES; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MOUTH NEOPLASMS; POLYMORPHISM, SINGLE NUCLEOTIDE; SMOKING; TAIWAN;

EID: 68949219476     PISSN: 13688375     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.oraloncology.2009.03.011     Document Type: Article

References (42)

1. Swango P.A. Cancers of the oral cavity and pharynx in the United States: an epidemiologic overview. J Public Health Dent 56 (1996) 309-318
2. Caplan D.J., and Hertz-Picciotto I. Racial differences in survival of oral and pharyngeal cancer patients in North Carolina. J Public Health Dent 58 (1998) 36-43
3. Shiboski C.H., Shiboski S.C., and Silverman S.J. Trends in oral cancer rates in the United States, 1973-1996. Community Dent Oral Epidemiol 28 (2000) 249-256
4. Moore R.J., Doherty D.A., Do K.A., Chamberlain R.M., and Khuri F.R. Racial disparity in survival of patients with squamous cell carcinoma of the oral cavity and pharynx. Ethn Health 6 (2001) 165-177
5. Department of Health, Taiwan: cancer registration system annual report. Taiwan, Department of Health; 2006.
6. Sugimura T., Kumimoto H., Tohnai I., Fukui T., Matsuo K., Tsurusako S., et al. Gene-environment interaction involved in oral carcinogenesis: molecular epidemiological study for metabolic and DNA repair gene polymorphisms. J Oral Pathol Med 35 (2006) 11-18
7. Vogelstein B., Alberts B., and Shine K. Genetics. Please don't call it cloning!. Science 295 (2002) 1237
8. Miller K.L., Karagas M.R., Kraft P., Hunter D.J., Catalano P.J., Byler S.H., et al. XPA, haplotypes, and risk of basal and squamous cell carcinoma. Carcinogenesis 27 (2006) 1670-1675
9. Hung R.J., Hall J., Brennan P., and Boffetta P. Genetic polymorphisms in the base excision repair pathway and cancer risk: a HuGE review. Am J Epidemiol 162 (2005) 925-942
10. Kirk B.W., Feinsod M., Favis R., Kliman R.M., and Barany F. Single nucleotide polymorphism seeking long term association with complex disease. Nucleic Acids Res 30 (2002) 3295-3311
11. Iyer R.R., Pluciennik A., Burdett V., and Modrich P.L. DNA mismatch repair: functions and mechanisms. Chem Rev 106 (2006) 302-323
12. Li G.M. DNA mismatch repair and cancer. Front Biosci 8 (2003) 997-1017
13. Wang Y.C., Lu Y.P., and Tseng R.C. Inactivation of hMLH1 and hMSH2 by promoter methylation in primary non-small cell lung tumors and matched sputum samples. J Clin Invest 111 (2003) 887-895
14. Xinarianos G., Liloglou T., and Prime W. hMLH1 and hMSH2 expression correlates with allelic imbalance on chromosome 3p in non-small cell lung carcinomas. Cancer Res 60 (2000) 4216-4221
15. Schmutte C., Marinescu R.C., Sadoff M.M., Guerrette S., Overhauser J., and Fishel R. Human exonuclease I interacts with the mismatch repair protein hMSH2. Cancer Res 58 (1998) 4537-4542
16. Tishkoff D.X., Amin N.S., Viars C.S., Arden K.C., and Kolodner R.D. Identification of a human gene encoding a homologue of Saccharomyces cerevisiae EXO1, an exonuclease implicated in mismatch repair and recombination. Cancer Res 58 (1998) 5027-5031
17. Wilson III D.M., Carney J.P., Coleman M.A., Adamson A.W., Christensen M., and Lamerdin J.E. Hex1: a new human Rad2 nuclease family member with homology to yeast exonuclease 1. Nucleic Acids Res 26 (1998) 3762-3768
18. Jager A.C., Rasmussen M., Bisgaard H.C., Singh K.K., Nielsen F.C., and Rasmussen L.J. HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLa and hMLH1-hEXO1 complexes. Oncogene 20 (2001) 3590-3595
19. Rasmussen L.J., Rasmussen M., and Lee B.I. Identification of factors interacting with hMSH2 in the fetal liver utilizing the yeast twohybrid system. In vivo interaction through the C-terminal domains of hEXO1 and hMSH2 and comparative expression analysis. Mutat Res 460 (2000) 41-52
20. Schmutte C., Sadoff M.M., Shim K.S., Acharya S., and Fishel R. The interaction of DNA mismatch repair proteins with human exonuclease I. J Biol Chem 276 (2001) 33011-33018
21. Tishkoff D.X., Boerger A.L., and Bertrand P. Identification and characterization of Saccharomyces cerevisiae EXO1, a gene encoding an exonuclease that interacts with MSH2. Proc Natl Acad Sci USA 94 (1997) 7487-7492
22. Tran P.T., Simon J.A., and Liskay R.M. Interactions of Exo1p with components of MutLa in Saccharomyces cerevisiae. Proc Natl Acad Sci USA 98 (2001) 9760-9765
23. Bau D.T., Fu Y.P., Chen S.T., Cheng T.C., Yu J.C., Wu P.E., et al. Breast cancer risk and the DNA double-strand break end-joining capacity of non-homologous end-joining genes are affected by BRCA1. Cancer Res 64 (2004) 5013-5019
24. Bau D.T., Mau Y.C., Ding S.L., Wu P.E., and Shen C.Y. DNA double-strand-break repair capacity and risk of breast cancer. Carcinogenesis 28 (2007) 1726-1730
25. Bau D.T., Tseng H.C., Wang C.H., Chiu C.F., Hua C.H., Wu C.N., et al. Oral cancer and genetic polymorphism of DNA double strand break gene Ku70 in Taiwan. Oral Oncol 44 (2008) 1047-1051
26. Chiu C.F., Tsai M.H., Tseng H.C., Wang C.L., Wang C.H., Wu C.N., et al. A novel single nucleotide polymorphism in XRCC4 gene is associated with oral cancer susceptibility in Taiwanese patients. Oral Oncol 44 (2008) 898-902
27. Chiu C.F., Wang H.C., Wang C.H., Wang C.L., Lin C.C., Shen C.Y., et al. A new single nucleotide polymorphism in XRCC4 gene is associated with breast cancer susceptibility in Taiwanese patients. Anticancer Res 28 (2008) 267-270
28. Chiu C.F., Wang C.H., Wang C.L., Lin C.C., Hsu N.Y., Weng J.R., et al. A novel single nucleotide polymorphism in XRCC4 gene is associated with oral cancer susceptibility in Taiwan. Ann Surg Oncol 15 (2008) 514-518
29. Chiu C.F., Tsai M.H., Tseng H.C., Wang C.L., Tsai F.J., Lin C.C., et al. A novel single nucleotide polymorphism in ERCC6 gene is associated with oral cancer susceptibility in Taiwanese patients. Oral Oncol 44 (2008) 582-586
30. Chiu C.F., Wang C.H., Wang C.L., Lin C.C., Hsu N.Y., Weng J.R., et al. A novel single nucleotide polymorphism in XRCC4 gene is associated with gastric cancer susceptibility in Taiwan. Ann Surg Oncol 15 (2008) 514-518
31. Wu C.N., Liang S.Y., Tsai C.W., and Bau D.T. The role of XRCC4 in carcinogenesis and anticancer drug discovery. Recent Patents Anti-Cancer Drug Discovery 3 (2008) 209-219
32. Marti T.M., Kunz C., and Fleck O. DNA mismatch repair and mutation avoidance pathways. J Cell Physiol 191 (2002) 28-41
33. Modrich P., and Lahue R. Mismatch repair in replication fidelity, genetic recombination, and cancer biology. Annu Rev Biochem 65 (1996) 101-133
34. Liberti S.E., and Rasmussen L.J. Is hEXO1 a cancer predisposing gene?. Mol Cancer Res 2 (2004) 427-432
35. Jagmohan-Changur S., Poikonen T., and Vilkki S. EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer. Cancer Res 63 (2003) 154-158
36. Thompson E., Meldrum C.J., and Crooks R. Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations. Clin Genet 65 (2004) 215-225
37. Wu Y., Berends M.J., and Post J.G. Germline mutations of EXO1 gene in patients with hereditary nonpolyposis colorectal cancer (HNPCC) and atypical HNPCC forms. Gastroenterology 120 (2001) 1580-1587
38. Yamamoto H., Hanafusa H., Ouchida M., Yano M., Suzuki H., and Murakami M. Single nucleotide polymorphisms in the EXO1 gene and risk of colorectal cancer in a Japanese population. Carcinogenesis 26 (2005) 411-416
39. Jin G., Wang H., and Hu Z. Potentially functional polymorphisms of EXO1 and risk of lung cancer in a Chinese population: a case-control analysis. Lung Cancer 60 (2008) 340-346
40. Zienolddiny S., Campa D., Lind H., Ryberg D., Skaug V., Stangeland L., et al. Polymorphisms of DNA repair genes and risk of non-small cell lung cancer. Carcinogenesis 27 (2006) 560-567
41. Chang J.S., Yeh R.F., Wiencke J.K., Wiemels J.L., Smirnov I., Pico A.R., et al. Pathway analysis of single-nucleotide polymorphisms potentially associated with glioblastoma multiforme susceptibility using random forests. Cancer Epidemiol Biomarkers Prev 17 (2008) 1368-1373
42. Jenab M., McKay J.D., Ferrari P., Biessy C., Laing S., Munar G.M., et al. CDH1 gene polymorphisms, smoking, Helicobacter pylori infection and the risk of oral cancer in the European Prospective Investigation into Cancer and Nutrition. Eur J Cancer 44 (2008) 774-780