Asian Pacific Journal of Cancer Prevention

Asian Pacific Journal of Cancer Prevention (아시아태평양암예방학회)
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RPSA Gene Mutants Associated with Risk of Colorectal Cancer among the Chinese Population

  • Zhang, Shan-Chun (Department of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University) ;
  • Jin, Wen (Department of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University) ;
  • Liu, Hui (Department of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University) ;
  • Jin, Ming-Juan (Department of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University) ;
  • Chen, Ze-Xin (Department of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University) ;
  • Ding, Zhe-Yuan (Department of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University) ;
  • Zheng, Shuang-Shuang (Department of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University) ;
  • Wang, Li-Juan (Department of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University) ;
  • Yu, Yun-Xian (Department of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University) ;
  • Chen, Kun (Department of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University)
  • Published : 2013.12.31
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Abstract

The primary aim of this study was to evaluate the relationship of single nucleotide polymorphisms (SNPs) in ribosomal protein SA (RPSA) gene with colorectal cancer (CRC). A case-control study including 388 controls and 387 patients with CRC was conducted in a Chinese population. Information about socio-demography and living behavior factors was collected by a structured questionnaire. Three SNPs (rs2133579, rs2269349, rs7641291) in RPSA gene were genotyped by Illumina SnapShot method. Multiple logistic regression models were used for assessing the joint effects between tea consumption and SNPs on CRC. The subjects with rs2269349 CC genotype had a decreased risk for CRC (OR=0.60; 95%CI = 0.37-0.99), compared with TT/CT genotype after adjustment for covariates. A similar association of rs2269349 with rectal cancer was observed (OR=0.49; 95%CI=0.24-1.00). Further analyses indicated that this SNP could modify the protective effect of tea drinking on CRC. Among the subjects with rs2269349 TT/CT or rs2133579 AA/GA, there was a marginal significantly lower risk of CRC (OR and 95%CI: 0.63 and 0.39-1.01 for rs2269349; 0.64 and 0.40-1.02 for rs2133579) in tea-drinking subjects in comparison to non-tea-drinking subjects. Mutants in the RPSA gene might be associated with genetic susceptibility to CRC and influence the protective effect of tea consumption in the Chinese population.

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References

  1. Akache B, Grimm D, Pandey K, et al (2006). The 37/67-kilodalton laminin receptor is a receptor for adeno-associated virus serotypes 8, 2, 3, and 9. J Virol, 80, 9831-6. https://doi.org/10.1128/JVI.00878-06
  2. Fujimura Y, Sumida M, Sugihara K, et al (2012). Green tea polyphenol EGCG sensing motif on the 67-kDa laminin receptor. PLoS One, 7, e37942. https://doi.org/10.1371/journal.pone.0037942
  3. Gauczynski S, Nikles D, El-Gogo S, et al (2006). The 37-kDa/67-kDa laminin receptor acts as a receptor for infectious prions and is inhibited by polysulfated glycanes. J Infect Dis, 194, 702-9. https://doi.org/10.1086/505914
  4. Gauczynski S, Peyrin JM, Haik S, et al (2001). The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein. EMBO J, 20, 5863-75. https://doi.org/10.1093/emboj/20.21.5863
  5. Hakim IA, Chow HH, Harris RB (2008). Green tea consumption is associated with decreased DNA damage among GSTM1-positive smokers regardless of their hOGG1 genotype. J Nutr, 138, S1567-71. https://doi.org/10.1093/jn/138.8.1567S
  6. Jamieson KV, Wu J, Hubbard SR, et al (2008). Crystal structure of the human laminin receptor precursor. J Biol Chem, 283, 3002-5. https://doi.org/10.1074/jbc.C700206200
  7. Ji BT, Chow WH, Hsing AW, et al (1997). Green tea consumption and the risk of pancreatic and colorectal cancers. Int J Cancer, 70, 255-8. https://doi.org/10.1002/(SICI)1097-0215(19970127)70:3<255::AID-IJC1>3.0.CO;2-W
  8. Kato I, Tominaga S, Matsuura A, et al (1990). A comparative case-control study of colorectal cancer and adenoma. Jpn J Cancer Res, 81, 1101-8. https://doi.org/10.1111/j.1349-7006.1990.tb02520.x
  9. Kawai Y, Matsui Y, Kondo H, et al (2008). Galloylated catechins as potent inhibitors of hypochlorous acid-induced DNA damage. Chem Res Toxicol, 21, 1407-14. https://doi.org/10.1021/tx800069e
  10. Kim KJ, Chung JW, Kim KS (2005). 67-kDa laminin receptor promotes internalization of cytotoxic necrotizing factor 1-expressing Escherichia coli K1 into human brain microvascular endothelial cells. J Biol Chem, 280, 1360-8. https://doi.org/10.1074/jbc.M410176200
  11. Kuzuhara T, Tanabe A, Sei Y, et al (2007). Synergistic effects of multiple treatments, and both DNA and RNA direct bindings on, green tea catechins. Mol Carcinog, 46, 640-5. https://doi.org/10.1002/mc.20332
  12. Lee KJ, Inoue M, Otani T, et al (2007). Coffee consumption and risk of colorectal cancer in a population-based prospective cohort of Japanese men and women. Int J Cancer, 121, 1312-8. https://doi.org/10.1002/ijc.22778
  13. Lin YL, Lin JK (1997). (-)-Epigallocatechin-3-gallate blocks the induction of nitric oxide synthase by down-regulating lipopolysaccharide-induced activity of transcription factor nuclear factor-kappaB. Mol Pharmacol, 52, 465-72. https://doi.org/10.1124/mol.52.3.465
  14. Martignone S, Menard S, Bufalino R, et al (1993). Prognostic significance of the 67-kilodalton laminin receptor expression in human breast carcinomas. J Natl Cancer Inst, 85, 398-402. https://doi.org/10.1093/jnci/85.5.398
  15. Menard S, Castronovo V, Tagliabue E, et al (1997). New insights into the metastasis-associated 67 kD laminin receptor. J Cell Biochem, 67, 155-65. https://doi.org/10.1002/(SICI)1097-4644(19971101)67:2<155::AID-JCB1>3.0.CO;2-W
  16. Nagano J, Kono S, Preston DL, et al (2001). A prospective study of green tea consumption and cancer incidence, Hiroshima and Nagasaki (Japan). Cancer Causes Control, 12, 501-8. https://doi.org/10.1023/A:1011297326696
  17. Nasiri H, Forouzandeh M, Rasaee MJ, et al (2005). Modified salting-out method: high-yield, high-quality genomic DNA extraction from whole blood using laundry detergent. J Clin Lab Anal, 19, 229-32. https://doi.org/10.1002/jcla.20083
  18. Qiao J, Su X, Wang Y, et al (2009). Cloning and characterization of full-length coding sequence (CDS) of the ovine 37/67-kDa laminin receptor (RPSA). Mol Biol Rep, 36, 2131-7. https://doi.org/10.1007/s11033-008-9426-x
  19. Sang S, Lee MJ, Hou Z, et al (2005). Stability of tea polyphenol (-)-epigallocatechin-3-gallate and formation of dimers and epimers under common experimental conditions. J Agric Food Chem, 53, 9478-84. https://doi.org/10.1021/jf0519055
  20. Siegel R, Naishadham D, Jemal A (2012). Cancer statistics, 2012. CA Cancer J Clin, 62, 10-29. https://doi.org/10.3322/caac.20138
  21. Sun CL, Yuan JM, Koh WP, et al (2007). Green tea and black tea consumption in relation to colorectal cancer risk: the Singapore Chinese Health Study. Carcinogenesis, 28, 2143-8. https://doi.org/10.1093/carcin/bgm171
  22. Sung JJ, Lau JY, Goh KL, et al (2005). Increasing incidence of colorectal cancer in Asia: implications for screening. Lancet Oncol, 6, 871-6. https://doi.org/10.1016/S1470-2045(05)70422-8
  23. Tachibana H, Koga K, Fujimura Y, et al (2004). A receptor for green tea polyphenol EGCG. Nat Struct Mol Biol, 11, 380-1. https://doi.org/10.1038/nsmb743
  24. Thepparit C, Smith DR (2004). Serotype-specific entry of dengue virus into liver cells: identification of the 37-kilodalton/67-kilodalton high-affinity laminin receptor as a dengue virus serotype 1 receptor. J Virol, 78, 12647-56. https://doi.org/10.1128/JVI.78.22.12647-12656.2004
  25. Tsukamoto S, Hirotsu K, Kumazoe M, et al (2012). Green tea polyphenol EGCG induces lipid-raft clustering and apoptotic cell death by activating protein kinase Cdelta and acid sphingomyelinase through a 67 kDa laminin receptor in multiple myeloma cells. Biochem J, 443, 525-34. https://doi.org/10.1042/BJ20111837
  26. Umeda D, Yano S, Yamada K, et al (2008). Green tea polyphenol epigallocatechin-3-gallate signaling pathway through 67-kDa laminin receptor. J Biol Chem, 283, 3050-8. https://doi.org/10.1074/jbc.M707892200
  27. Wang ZY, Cheng SJ, Zhou ZC, et al (1989). Antimutagenic activity of green tea polyphenols. Mutat Res, 223, 273-85. https://doi.org/10.1016/0165-1218(89)90120-1
  28. Yang G, Shu XO, Li H, et al (2007). Prospective cohort study of green tea consumption and colorectal cancer risk in women. Cancer Epidemiol Biomarkers Prev, 16, 1219-23. https://doi.org/10.1158/1055-9965.EPI-07-0097
  29. Yang L, Parkin DM, Ferlay J, et al (2005). Estimates of cancer incidence in China for 2000 and projections for 2005. Cancer Epidemiol Biomarkers Prev, 14, 243-50.
  30. Zhang X, Albanes D, Beeson WL, et al (2010). Risk of colon cancer and coffee, tea, and sugar-sweetened soft drink intake: pooled analysis of prospective cohort studies. J Natl Cancer Inst, 102, 771-83. https://doi.org/10.1093/jnci/djq107
  31. Zhang Y, Liu B, Jin M, et al (2009). Genetic polymorphisms of transforming growth factor-beta1 and its receptors and colorectal cancer susceptibility: a population-based casecontrol study in China. Cancer Lett, 275, 102-8. https://doi.org/10.1016/j.canlet.2008.10.017

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