Abstract
Purpose
The primary aim was to respectively evaluate PLA2G4A mutants modifying protective effect of tea consumption against colorectal cancer (CRC), colon and rectal cancer.
Methods
All participants were recruited from January 2006 to April 2008. The information about tea consumption was collected by a structured questionnaire. CRC patients were diagnosed based on histology. Four single-nuclear polymorphisms (SNPs) in PLA2G4A gene were selected. Multiple logistic regression models were used for assessing the joint effects between tea consumption and SNPs on CRC, colon and rectal cancer.
Results
Three hundred patients with CRC and 296 controls well-matched were used in the final analyses. The significant individual associations between four SNPs (rs6666834, rs10911933, rs4650708 and rs7526089) and CRC were not observed. However, their CTAC haplotype was significantly associated with the increased risk of CRC (OR = 3.06; 95%CI = 1.52–6.19), compared with TCAC haplotype. Drinking tea was correlated with a decreased risk of CRC after adjustment for covariates (OR = 0.61; 95%CI = 0.39–0.97). Meanwhile, compared with no-tea drinkers with TT/CT genotype of rs6666834, tea drinkers with TT/CT or CC had significant lower risk of CRC (OR = 0.6, 95%CI = 0.36–1.00 for TT/CT; 0.38, 0.19–0.74 for CC). The joint effects between the remaining three SNPs and drinking tea on CRC were observed as well. Similar findings were observed on colon and rectal cancers.
Conclusions
Tea consumption and haplotype of mutants in PLA2G4A gene were respectively associated with the risk of CRC. PLA2G4A mutants modified the protective effect of tea consumption against CRC, colon and rectal cancers in Chinese population.
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References
Ferlay J, Bray F, Pisani P, Parkin DM (2004). GLOBOCAN 2002: cancer incidence, mortality and prevalence worldwide: Lyon, France
Sung JJ, Lau JY, Goh KL, Leung WK (2005) Increasing incidence of colorectal cancer in Asia: implications for screening. Lancet Oncol 6(11):871–6
Yang L, Parkin DM, Ferlay J, Li L, Chen Y (2005) Estimates of cancer incidence in China for 2000 and projections for 2005. Cancer Epidemiol Biomarkers Prev 14(1):243–50
Word Cancer Research Fund AIfCREP (2007) Food, nutrition and the prevention of cancer: a global perspective. Washington DAIfCR, editor
Anderson RF, Fisher LJ, Hara Y et al (2001) Green tea catechins partially protect DNA from (.)OH radical-induced strand breaks and base damage through fast chemical repair of DNA radicals. Carcinogenesis 22(8):1189–93
Lim YC, Lee SH, Song MH et al (2006) Growth inhibition and apoptosis by (−)-epicatechin gallate are mediated by cyclin D1 suppression in head and neck squamous carcinoma cells. Eur J Cancer 42(18):3260–6
Inoue M, Tajima K, Hirose K et al (1998) Tea and coffee consumption and the risk of digestive tract cancers: data from a comparative case-referent study in Japan. Cancer Causes Control 9(2):209–16
Kato I, Tominaga S, Matsuura A, Yoshii Y, Shirai M, Kobayashi S (1990) A comparative case–control study of colorectal cancer and adenoma. Jpn J Cancer Res 81(11):1101–8
Slattery ML, Caan BJ, Anderson KE, Potter JD (1999) Intake of fluids and methylxanthine-containing beverages: association with colon cancer. Int J Cancer 81(2):199–204
Franceschi S, Favero A, La Vecchia C et al (1997) Food groups and risk of colorectal cancer in Italy. Int J Cancer 72(1):56–61
Woolcott CG, King WD, Marrett LD (2002) Coffee and tea consumption and cancers of the bladder, colon and rectum. Eur J Cancer Prev 11(2):137–45
Baron JA, Gerhardsson de Verdier M, Ekbom A (1994) Coffee, tea, tobacco, and cancer of the large bowel. Cancer Epidemiol Biomarkers Prev 3(7):565–70
Cerhan JR, Putnam SD, Bianchi GD, Parker AS, Lynch CF, Cantor KP (2001) Tea consumption and risk of cancer of the colon and rectum. Nutr Cancer 41(1–2):33–40
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(11):771–83
Ji BT, Chow WH, Hsing AW et al (1997) Green tea consumption and the risk of pancreatic and colorectal cancers. Int J Cancer 70(3):255–8
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(6):1219–23
Lee KJ, Inoue M, Otani T, Iwasaki M, Sasazuki S, Tsugane S (2007) Coffee consumption and risk of colorectal cancer in a population-based prospective cohort of Japanese men and women. Int J Cancer 121(6):1312–8
Sun CL, Yuan JM, Koh WP, Lee HP, Yu MC (2007) Green tea and black tea consumption in relation to colorectal cancer risk: the Singapore Chinese Health Study. Carcinogenesis 28(10):2143–8
Nagano J, Kono S, Preston DL, Mabuchi K (2001) A prospective study of green tea consumption and cancer incidence, Hiroshima and Nagasaki (Japan). Cancer Causes Control 12(6):501–8
Tajima K, Tominaga S (1985) Dietary habits and gastro-intestinal cancers: a comparative case–control study of stomach and large intestinal cancers in Nagoya, Japan. Jpn J Cancer Res 76(8):705–16
Moran EM (2002) Epidemiological and clinical aspects of nonsteroidal anti-inflammatory drugs and cancer risks. J Environ Pathol Toxicol Oncol 21(2):193–201
Pereira C, Pimentel-Nunes P, Brandao C, Moreira-Dias L, Medeiros R, Dinis-Ribeiro M. COX-2 polymorphisms and colorectal cancer risk: a strategy for chemoprevention. Eur J Gastroenterol Hepatol 22(5):607–613
Herbert SP, Odell AF, Ponnambalam S, Walker JH (2007) The confluence-dependent interaction of cytosolic phospholipase A2-alpha with annexin A1 regulates endothelial cell prostaglandin E2 generation. J Biol Chem 282(47):34468–78
Balsinde J, Winstead MV, Dennis EA (2002) Phospholipase A(2) regulation of arachidonic acid mobilization. FEBS Lett 531(1):2–6
Kita Y, Ohto T, Uozumi N, Shimizu T (2006) Biochemical properties and pathophysiological roles of cytosolic phospholipase A2s. Biochim Biophys Acta 1761(11):1317–22
Ju J, Liu Y, Hong J, Huang MT, Conney AH, Yang CS (2003) Effects of green tea and high-fat diet on arachidonic acid metabolism and aberrant crypt foci formation in an azoxymethane-induced colon carcinogenesis mouse model. Nutr Cancer 46(2):172–8
Fan C, Jin M, Chen K, Zhang Y, Zhang S, Liu B (2007) Case-only study of interactions between metabolic enzymes and smoking in colorectal cancer. BMC Cancer 7:115
Dannenberg AJ, Altorki NK, Boyle JO et al (2001) Cyclo-oxygenase 2: a pharmacological target for the prevention of cancer. Lancet Oncol 2(9):544–51
Lim SC, Cho H, Lee TB et al (2010) Impacts of cytosolic phospholipase A2, 15-prostaglandin dehydrogenase, and cyclooxygenase-2 expressions on tumor progression in colorectal cancer. Yonsei Med J 51(5):692–9
Pae CU, Yu HS, Lee KU et al (2004) BanI polymorphism of the cytosolic phospholipase A2 gene may confer susceptibility to the development of schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry 28(4):739–41
Umeno J, Matsumoto T, Esaki M and others. Impact of group IVA cytosolic phospholipase A2 gene polymorphisms on phenotypic features of patients with familial adenomatous polyposis. Int J Colorectal Dis 25(3):293–301
Acknowledgment
The study was funded, in part, by grants from the Natural Science Foundation of Zhejiang Province (Y2090154), New Teacher Foundation of Ministry of Education (20090101120103), Department of Education of Zhejiang Province (Z200804565) and Zhejiang Foundation of Young Teachers’ innovation (2009QNA7018).
We thank the staff of the Cancer Institute of Jiashan County for their continuous support and assistance to collect the epidemiological data and blood specimen. We would like to particularly thank all participants and their family for their contributions and supports.
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Yu, Y., Zhang, M., Pan, Y. et al. PLA2G4A mutants modified protective effect of tea consumption against colorectal cancer. Int J Colorectal Dis 27, 1005–1013 (2012). https://doi.org/10.1007/s00384-012-1417-7
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DOI: https://doi.org/10.1007/s00384-012-1417-7