Gene-diet interaction between SIRT6 and soybean intake for different levels of pulse wave velocity

International Journal of Molecular Sciences

Volumn 16, Issue 7, 2015, Pages 14338-14352

  Sun, Kexin ^a   Xiang, Xiao ^a   Li, Na ^b   Huang, Shaoping ^b   Qin, Xueying ^a   Wu, Yiqun ^a   Tang, Xun ^a   Gao, Pei ^a   Li, Jing ^a   Wu, Tao ^a   Chen, Dafang ^a   Hu, Yonghua ^a  

^a PEKING UNIVERSITY HEALTH SCIENCE CENTER   (China)

^b CHINESE CENTER FOR DISEASE CONTROL AND PREVENTION   (China)

Author keywords

ADIPOQ; Atherosclerosis; Brachial ankle pulse wave velocity; Genetic polymorphisms; Inflammation; Interaction; SIRT6; Soybean

Indexed keywords

ADIPONECTIN; ARYLDIALKYLPHOSPHATASE 1; CADHERIN 13; CHEMOKINE RECEPTOR CXCR4; CHOLESTEROL; CYCLIN DEPENDENT KINASE INHIBITOR 2B; GLUCOSE; GLYCOPROTEIN; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; LOW DENSITY LIPOPROTEIN CHOLESTEROL; NEURONAL NITRIC OXIDE SYNTHASE; SIRTUIN 3; SIRTUIN 6; STROMAL CELL DERIVED FACTOR 1; TRIACYLGLYCEROL; UNCLASSIFIED DRUG; ADIPOQ PROTEIN, HUMAN; SIRT6 PROTEIN, HUMAN; SIRTUIN; SOYBEAN PROTEIN;

ADULT; ANTHROPOMETRY; ARTICLE; BIOCHEMISTRY; CROSS-SECTIONAL STUDY; DIETARY INTAKE; ENVIRONMENTAL FACTOR; FEMALE; GENE INTERACTION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOTYPE; HUMAN; MALE; MIDDLE AGED; PULSE WAVE; SOYBEAN; AGED; DRUG EFFECTS; GENE LOCUS; GENETICS; GENOTYPE ENVIRONMENT INTERACTION; HEMODYNAMICS; SINGLE NUCLEOTIDE POLYMORPHISM;

GLYCINE MAX;

ADIPONECTIN; AGED; FEMALE; GENE-ENVIRONMENT INTERACTION; GENETIC LOCI; HEMODYNAMICS; HUMANS; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PULSE WAVE ANALYSIS; SIRTUINS; SOYBEAN PROTEINS;

EID: 84933567430     PISSN: 16616596     EISSN: 14220067     Source Type: Journal    
DOI: 10.3390/ijms160714338     Document Type: Article

References (53)

1. Bramwell, J.C.; Hill, A. Velocity of transmission of the pulse-wave: And elasticity of arteries. Lancet 1922, 199, 891–892
2. O’Rourke, M.F.; Mancia, G. Arterial stiffness. J. Hypertens. 1999, 17, 1–4
3. Blacher, J.; Asmar, R.; Djane, S.; London, G.M.; Safar, M.E. Aortic pulse wave velocity as a marker of cardiovascular risk in hypertensive patients. Hypertension 1999, 33, 1111–1117
4. Epstein, F.H.; Ross, R. Atherosclerosis—An inflammatory disease. N. Engl. J. Med. 1999, 340, 115–126
5. Hansson, G.K. Inflammation, atherosclerosis, and coronary artery disease. N. Engl. J. Med. 2005, 352, 1685–1695
6. Stone, G.W.; Maehara, A.; Lansky, A.J.; de Bruyne, B.; Cristea, E.; Mintz, G.S.; Mehran, R.; McPherson, J.; Farhat, N.; Marso, S.P.; et al. A prospective natural-history study of coronary atherosclerosis. N. Engl. J. Med. 2011, 364, 226–235
7. Angelovich, T.A.; Hearps, A.C.; Jaworowski, A. Inflammation-induced foam cell formation in chronic inflammatory disease. Immunol. Cell Biol. 2015, doi:10.1038/icb.2015.26
8. McPherson, R.; Davies, R.W. Inflammation and coronary artery disease: Insights from genetic studies. Can. J. Cardiol. 2012, 28, 662–666
9. McPherson, R.; Pertsemlidis, A.; Kavaslar, N.; Stewart, A.; Roberts, R.; Cox, D.R.; Hinds, D.A.; Pennacchio, L.A.; Tybjaerg-Hansen, A.; Folsom, A.R.; et al. A common allele on chromosome 9 associated with coronary heart disease. Science 2007, 316, 1488–1491
10. Helgadottir, A.; Thorleifsson, G.; Manolescu, A.; Gretarsdottir, S.; Blondal, T.; Jonasdottir, A.; Jonasdottir, A.; Sigurdsson, A.; Baker, A.; Palsson, A.; et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 2007, 316, 1491–1493
11. Samani, N.J.; Erdmann, J.; Hall, A.S.; Hengstenberg, C.; Mangino, M.; Mayer, B.; Dixon, R.J.; Meitinger, T.; Braund, P.; Wichmann, H.E.; et al. Genomewide association analysis of coronary artery disease. N. Engl. J. Med. 2007, 357, 443–453
12. Hu, E.; Liang, P.; Spiegelman, B.M. ADIPOQ is a novel adipose-specific gene dysregulated in obesity. J. Biol. Chem. 1996, 271, 10697–10703
13. Ouchi, N.; Kihara, S.; Funahashi, T.; Matsuzawa, Y.; Walsh, K. Obesity, adiponectin and vascular inflammatory disease. Curr. Opin. Lipidol. 2003, 14, 561–566
14. Wassel, C.L.; Pankow, J.S.; Rasmussen-Torvik, L.J.; Li, N.; Taylor, K.D.; Guo, X.; Goodarzi, M.O.; Palmas, W.R.; Post, W.S. Associations of SNPs in ADIPOQ and subclinical cardiovascular disease in the multi-ethnic study of atherosclerosis (MESA). Obesity 2011, 19, 840–847
15. Hug, C.; Wang, J.; Ahmad, N.S.; Bogan, J.S.; Tsao, T.S.; Lodish, H.F. T-cadherin is a receptor for hexameric and high-molecular-weight forms of Acrp30/adiponectin. Proc. Natl. Acad. Sci. USA 2004, 101, 10308–10313
16. Takeuchi, T.; Adachi, Y.; Ohtsuki, Y.; Furihata, M. Adiponectin receptors, with special focus on the role of the third receptor, T-cadherin, in vascular disease. Med. Mol. Morphol. 2007, 40, 115–120
17. Imai, S.; Armstrong, C.M.; Kaeberlein, M.; Guarente, L. Transcriptional silencing and longevity protein Sir2 is an nad-dependent histone deacetylase. Nature 2000, 403, 795–800
18. Liu, G.; Cao, M.; Xu, Y.; Li, Y. Sirt3 protects endothelial cells from high glucose-induced cytotoxicity. Int. J. Clin. Exp. Pathol. 2015, 8, 353–360
19. Webster, K.A. A sirtuin link between metabolism and heart disease. Nat. Med. 2012, 18, 1617–1619
20. Sundaresan, N.R.; Vasudevan, P.; Zhong, L.; Kim, G.; Samant, S.; Parekh, V.; Pillai, V.B.; Ravindra, P.V.; Gupta, M.; Jeevanandam, V.; et al. The sirtuin SIRT6 blocks IGF-Akt signaling and development of cardiac hypertrophy by targeting c-Jun. Nat. Med. 2012, 18, 1643–1650
21. Kugel, S.; Mostoslavsky, R. Chromatin and beyond: The multitasking roles for SIRT6. Trends Biochem. Sci. 2014, 39, 72–81
22. Zernecke, A.; Shagdarsuren, E.; Weber, C. Chemokines in atherosclerosis: An update. Arterioscler. Thromb. Vasc. Biol. 2008, 28, 1897–1908
23. Breton, C.V.; Park, C.; Siegmund, K.; Gauderman, W.J.; Whitfield-Maxwell, L.; Hodis, H.N.; Avol, E.; Gilliland, F.D. NOS1 methylation and carotid artery intima-media thickness in children. Circ. Cardiovasc. Genet. 2014, 7, 116–122
24. Liu, T.; Zhang, X.; Zhang, J.; Liang, Z.; Cai, W.; Huang, M.; Yan, C.; Zhu, Z.; Han, Y. Association between PON1 rs662 polymorphism and coronary artery disease. Eur. J. Clin. Nutr. 2014, 68, 1029–1035
25. Madssen, E.; Videm, V.; Moholdt, T.; Wisloff, U.; Hegbom, K.; Wiseth, R. Predictors of beneficial coronary plaque changes following aerobic exercise. Med. Sci. Sports Exerc. 2015, in press
26. Van Bussel, B.C.; Henry, R.M.; Ferreira, I.; van Greevenbroek, M.M.; van der Kallen, C.J.; Twisk, J.W.; Feskens, E.J.; Schalkwijk, C.G.; Stehouwer, C.D. A healthy diet is associated with less endothelial dysfunction and less low-grade inflammation over a 7-year period in adults at risk of cardiovascular disease. J. Nutr. 2015, 145, 532–540
27. Yamori, Y. Food factors for atherosclerosis prevention: Asian perspective derived from analyses of worldwide dietary biomarkers. Exp. Clin. Cardiol. 2006, 11, 94–98
28. Cortez-Cooper, M.Y.; Supak, J.A.; Tanaka, H. A new device for automatic measurements of arterial stiffness and ankle-brachial index. Am. J. Cardiol. 2003, 91, 1519–1522
29. Kobayashi, K.; Akishita, M.; Yu, W.; Hashimoto, M.; Ohni, M.; Toba, K. Interrelationship between non-invasive measurements of atherosclerosis: Flow-mediated dilation of brachial artery, carotid intima-media thickness and pulse wave velocity. Atherosclerosis 2004, 173, 13–18
30. Ong, K.L.; Li, M.; Tso, A.W.; Xu, A.; Cherny, S.S.; Sham, P.C.; Tse, H.F.; Lam, T.H.; Cheung, B.M.; Lam, K.S. Association of genetic variants in the adiponectin gene with adiponectin level and hypertension in hong kong chinese. Eur. J. Endocrinol. 2010, 163, 251–257
31. Shi, H.; Lu, Y.; Du, J.; Du, W.; Ye, X.; Yu, X.; Ma, J.; Cheng, J.; Gao, Y.; Cao, Y.; et al. Application of back propagation artificial neural network on genetic variants in adiponectin ADIPOQ, peroxisome proliferator-activated receptor-γ, and retinoid x receptor-α genes and type 2 diabetes risk in a chinese han population. Diabetes Technol. Ther. 2012, 14, 293–300
32. Sanghera, D.K.; Demirci, F.Y.; Been, L.; Ortega, L.; Ralhan, S.; Wander, G.S.; Mehra, N.K.; Singh, J.; Aston, C.E.; Mulvihill, J.J.; et al. PPARG and ADIPOQ gene polymorphisms increase type 2 diabetes mellitus risk in asian indian Sikhs: Pro12Ala still remains as the strongest predictor. Metabolism 2010, 59, 492–501
33. Liszt, G.; Ford, E.; Kurtev, M.; Guarente, L. Mouse Sir2 homolog SIRT6 is a nuclear ADP-ribosyltransferase. J. Biol. Chem. 2005, 280, 21313–21320
34. Zhong, L.; D'Urso, A.; Toiber, D.; Sebastian, C.; Henry, R.E.; Vadysirisack, D.D.; Guimaraes, A.; Marinelli, B.; Wikstrom, J.D.; Nir, T et al. The histone deacetylase SIRT6 regulates glucose homeostasis via HIF1α. Cell 2010, 140, 280–293
35. Kim, H.S.; Xiao, C.; Wang, R.H.; Lahusen, T.; Xu, X.; Vassilopoulos, A.; Vazquez-Ortiz, G.; Jeong, W.I.; Park, O.; Ki, S.H et al. Hepatic specific disruption of SIRT6 in mice results in fatty liver formation due to enhanced glycolysis and triglyceride synthesis. Cell Metab. 2010, 12, 224–236
36. Yao, Q.P.; Zhang, P.; Qi, Y.X.; Chen, S.G.; Shen, B.R.; Han, Y.; Yan, Z.Q.; Jiang, Z.L. The role of SIRT6 in the differentiation of vascular smooth muscle cells in response to cyclic strain. Int. J. Biochem. Cell Biol. 2014, 49, 98–104
37. TenNapel, M.J.; Lynch, C.F.; Burns, T.L.; Wallace, R.; Smith, B.J.; Button, A.; Domann, F.E. SIRT6 minor allele genotype is associated with >5-year decrease in lifespan in an aged cohort. PLoS ONE 2014, 9, e115616
38. Dong, C.; Della-Morte, D.; Wang, L.; Cabral, D.; Beecham, A.; McClendon, M.S.; Luca, C.C.; Blanton, S.H.; Sacco, R.L.; Rundek, T. Association of the sirtuin and mitochondrial uncoupling protein genes with carotid plaque. PLoS ONE 2011, 6, e27157
39. Maeda, S.; Koya, D.; Araki, S.-I.; Babazono, T.; Umezono, T.; Toyoda, M.; Kawai, K.; Imanishi, M.; Uzu, T.; Suzuki, D. Association between single nucleotide polymorphisms within genes encoding sirtuin families and diabetic nephropathy in Japanese subjects with type 2 diabetes. Clin. Exp. Nephrol. 2011, 15, 381–390
40. Rosenson, R.S.; Fioretto, P.; Dodson, P.M. Does microvascular disease predict macrovascular events in type 2 diabetes? Atherosclerosis 2011, 218, 13–18
41. Wei, P.; Liu, M.; Chen, Y.; Chen, D.-C. Systematic review of soy isoflavone supplements on osteoporosis in women. Asian Pac. J. Trop. Med. 2012, 5, 243–248
42. Huang, C.C.; Hsu, B.Y.; Wu, N.L.; Tsui, W.H.; Lin, T.J.; Su, C.C.; Hung, C.F. Anti-photoaging effects of soy isoflavone extract (aglycone and acetylglucoside form) from soybean cake. Int. J. Mol. Sci. 2010, 11, 4782–4795
43. Kao, T.H.; Huang, R.F.S.; Chen, B.H. Antiproliferation of hepatoma cell and progression of cell cycle as affected by isoflavone extracts from soybean cake. Int. J. Mol. Sci. 2007, 8, 1095–1110
44. Wang, Q.; Li, H.; Tao, P.; Wang, Y.P.; Yuan, P.; Yang, C.X.; Li, J.Y.; Yang, F.; Lee, H.; Huang, Y. Soy isoflavones, CYP1A1, CYP1B1, and COMT polymorphisms, and breast cancer: A case-control study in southwestern china. DNA Cell Biol. 2011, 30, 585–595
45. Xu, W.H.; Zheng, W.; Cai, Q.; Cheng, J.R.; Cai, H.; Xiang, Y.B.; Shu, X.O. The Asp(327)Asn polymorphism in the sex hormone-binding globulin gene modifies the association of soy food and tea intake with endometrial cancer risk. Nutr. Cancer 2008, 60, 736–743
46. Deming, S.L.; Zheng, W.; Xu, W.H.; Cai, Q.; Ruan, Z.; Xiang, Y.B.; Shu, X.O. UGT1A1 genetic polymorphisms, endogenous estrogen exposure, soy food intake, and endometrial cancer risk. Cancer Epidemiol. Biomark. Prev. 2008, 17, 563–570
47. Wang, J.W.; Tang, X.; Li, N.; Wu, Y.Q.; Li, S.; Li, J.; Qin, X.Y.; Zhang, Z.X.; Hu, Y.H.; Chen da, F. The impact of lipid-metabolizing genetic polymorphisms on body mass index and their interactions with soybean food intake: A study in a chinese population. Biomed. Environ. Sci. 2014, 27, 176–185
48. Serrano, J.C.; de Lorenzo, D.; Cassanye, A.; Martin-Gari, M.; Espinel, A.; Delgado, M.A.; Pamplona, R.; Portero-Otin, M. Vitamin D receptor BSMI polymorphism modulates soy intake and 25-hydroxyvitamin d supplementation benefits in cardiovascular disease risk factors profile. Genes Nutr. 2013, 8, 561–569
49. Kuiper, G.G.; Lemmen, J.G.; Carlsson, B.; Corton, J.C.; Safe, S.H.; van der Saag, P.T.; van der Burg, B.; Gustafsson, J.A. Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor β. Endocrinology 1998, 139, 4252–4263
50. Shu, X.O.; Yang, G.; Jin, F.; Liu, D.; Kushi, L.; Wen, W.; Gao, Y.T.; Zheng, W. Validity and reproducibility of the food frequency questionnaire used in the shanghai women’s health study. Eur. J. Clin. Nutr. 2004, 58, 17–23
51. Yamashina, A.; Tomiyama, H.; Takeda, K.; Tsuda, H.; Arai, T.; Hirose, K.; Koji, Y.; Hori, S.; Yamamoto, Y. Validity, reproducibility, and clinical significance of noninvasive brachial-ankle pulse wave velocity measurement. Hypertens. Res. 2002, 25, 359–364
52. Tomiyama, H.; Koji, Y.; Yambe, M.; Shiina, K.; Motobe, K.; Yamada, J.; Shido, N.; Tanaka, N.; Chikamori, T.; Yamashina, A. Brachial—Ankle pulse wave velocity is a simple and independent predictor of prognosis in patients with acute coronary syndrome. Circ. J. 2005, 69, 815–822
53. Lewis, C.M. Genetic association studies: Design, analysis and interpretation. Brief. Bioinform. 2002, 3, 146–153.