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Inhibitory effects of calcium against intestinal cancer in human colon cancer cells and $Apc^{Min/+}$ mice

  • Ju, Jihyeung (Department of Food and Nutrition, Chungbuk National University) ;
  • Kwak, Youngeun (Department of Food and Nutrition, Chungbuk National University) ;
  • Hao, Xingpei (Susan Lehman Cullman Laboratory for Cancer Research, Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey) ;
  • Yang, Chung S. (Susan Lehman Cullman Laboratory for Cancer Research, Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey)
  • Received : 2012.06.21
  • Accepted : 2012.08.06
  • Published : 2012.10.31

Abstract

The aim of the study was to investigate the inhibitory effects of calcium against intestinal cancer in vitro and in vivo. We first investigated the effects of calcium treatment in HCT116 and HT29 human colon cancer cells. At the concentration range of 0.8-2.4 mM, calcium significantly inhibited cell growth (by 9-29%), attachment (by 12-26%), invasion (by 15-31%), and migration (by 19-61%). An immunofluorescence microscope analysis showed that the treatment with calcium (1.6 mM) for 24 h increased plasma membrane ${\beta}$-catenin but decreased nuclear ${\beta}$-catenin levels in HT29 cells. We then investigated the effect of dietary calcium on intestinal tumorigenesis in $Apc^{Min/+}$ mice. Mice received dietary treatment starting at 6 weeks of age for the consecutive 8 weeks. The basal control diet contained high-fat (20% mixed lipids by weight) and low-calcium (1.4 mg/g diet) to mimic the average Western diet, while the treatment diet contained an enriched level of calcium (5.2 mg calcium/g diet). The dietary calcium treatment decreased the total number of small intestinal tumors (by 31.4%; P < 0.05). The largest decrease was in tumors which were ${\geq}$ 2 mm in diameter, showing a 75.6% inhibition in the small intestinal tumor multiplicity (P < 0.001). Immunohistochemical analysis showed significantly reduced nuclear staining of ${\beta}$-catenin (expressed as nuclear positivity), but increased plasma membrane staining of ${\beta}$-catenin, in the adenomas from the calcium-treated groups in comparison to those from the control group (P < 0.001). These results demonstrate intestinal cancer inhibitory effects of calcium both in human colon cancer cells and $Apc^{Min/+}$ mice. The decreased ${\beta}$-catenin nuclear localization caused by the calcium treatment may contribute to the inhibitory action.

Keywords

References

  1. Boyle P, Levin B. World Cancer Report 2008. Geneva: WHO Press; 2008. p.11-55.
  2. McCullough ML, Giovannucci EL. Diet and cancer prevention. Oncogene 2004;23:6349-64. https://doi.org/10.1038/sj.onc.1207716
  3. Straub DA. Calcium supplementation in clinical practice: a review of forms, doses, and indications. Nutr Clin Pract 2007;22:286-96. https://doi.org/10.1177/0115426507022003286
  4. Chia V, Newcomb PA. Calcium and colorectal cancer: some questions remain. Nutr Rev 2004;62:115-20.
  5. Lamprecht SA, Lipkin M. Chemoprevention of colon cancer by calcium, vitamin D and folate: molecular mechanisms. Nat Rev Cancer 2003;3:601-14.
  6. Half E, Arber N. Colon cancer: preventive agents and the present status of chemoprevention. Expert Opin Pharmacother 2009;10:211-9. https://doi.org/10.1517/14656560802560153
  7. Carroll C, Cooper K, Papaioannou D, Hind D, Pilgrim H, Tappenden P. Supplemental calcium in the chemoprevention of colorectal cancer: a systematic review and meta-analysis. Clin Ther 2010;32:789-803. https://doi.org/10.1016/j.clinthera.2010.04.024
  8. Baron JA, Beach M, Mandel JS, van Stolk RU, Haile RW, Sandler RS, Rothstein R, Summers RW, Snover DC, Beck GJ, Bond JH, Greenberg ER. Calcium supplements for the prevention of colorectal adenomas. Calcium Polyp Prevention Study Group. N Engl J Med 1999;340:101-7. https://doi.org/10.1056/NEJM199901143400204
  9. Wallace K, Baron JA, Cole BF, Sandler RS, Karagas MR, Beach MA, Haile RW, Burke CA, Pearson LH, Mandel JS, Rothstein R, Snover DC. Effect of calcium supplementation on the risk of large bowel polyps. J Natl Cancer Inst 2004;96:921-5. https://doi.org/10.1093/jnci/djh165
  10. Kenar L, Karayilanoglu T, Aydin A, Serdar M, Kose S, Erbil MK. Protective effects of diets supplemented with omega-3 polyunsaturated fatty acids and calcium against colorectal tumor formation. Dig Dis Sci 2008;53:2177-82. https://doi.org/10.1007/s10620-007-0107-8
  11. Belbraouet S, Felden F, Pelletier X, Gastin I, Lambert D, Floquet J, Gueant JL, Debry G. Dietary calcium salts as protective agents and laminin P1 as a biochemical marker in chemically induced colon carcinogenesis in rats. Cancer Detect Prev 1996;20:294-9.
  12. Ranhotra GS, Gelroth JA, Glaser BK, Schoening P, Brown SE. Cellulose and calcium lower the incidence of chemically-induced colon tumors in rats. Plant Foods Hum Nutr 1999;54:295-303. https://doi.org/10.1023/A:1008149107282
  13. Pence BC, Dunn DM, Zhao C, Landers M, Wargovich MJ. Chemopreventive effects of calcium but not aspirin supplementation in cholic acid-promoted colon carcinogenesis: correlation with intermediate endpoints. Carcinogenesis 1995;16:757-65. https://doi.org/10.1093/carcin/16.4.757
  14. Vinas-Salas J, Biendicho-Palau P, Piñol-Felis C, Miguelsanz Garcia S, Perez-Holanda S. Calcium inhibits colon carcinogenesis in an experimental model in the rat. Eur J Cancer 1998;34: 1941-5. https://doi.org/10.1016/S0959-8049(98)00197-X
  15. Dwivedi C, Oredipe OA, Barth RF, Downie AA, Webb TE. Effects of the experimental chemopreventative agent, glucarate, on intestinal carcinogenesis in rats. Carcinogenesis 1989;10: 1539-41. https://doi.org/10.1093/carcin/10.8.1539
  16. Wargovich MJ, Allnutt D, Palmer C, Anaya P, Stephens LC. Inhibition of the promotional phase of azoxymethane-induced colon carcinogenesis in the F344 rat by calcium lactate: effect of simulating two human nutrient density levels. Cancer Lett 1990;53:17-25. https://doi.org/10.1016/0304-3835(90)90005-I
  17. Karkare MR, Clark TD, Glauert HP. Effect of dietary calcium on colon carcinogenesis induced by a single injection of 1,2-dimethylhydrazine in rats. J Nutr 1991;121:568-77.
  18. Adell-Carceller R, Segarra-Soria M, Gibert-Jerez J, Salvador Sanchís JL, Lazaro-Santander R, Escrig-Sos J, Ruiz-Castillo J. Inhibitory effect of calcium on carcinogenesis at the site of colonic anastomosis: an experimental study. Dis Colon Rectum 1997;40:1376-81. https://doi.org/10.1007/BF02050826
  19. Pereira MA, Barnes LH, Rassman VL, Kelloff GV, Steele VE. Use of azoxymethane-induced foci of aberrant crypts in rat colon to identify potential cancer chemopreventive agents. Carcinogenesis 1994;15:1049-54. https://doi.org/10.1093/carcin/15.5.1049
  20. Liu Z, Tomotake H, Wan G, Watanabe H, Kato N. Combined effect of dietary calcium and iron on colonic aberrant crypt foci, cell proliferation and apoptosis, and fecal bile acids in 1,2-dimethylhydrazine-treated rats. Oncol Rep 2001;8:893-7.
  21. Molck AM, Poulsen M, Meyer O. The combination of 1alpha,25 (OH2)-vitamin D3, calcium and acetylsalicylic acid affects azoxymethane-induced aberrant crypt foci and colorectal tumours in rats. Cancer Lett 2002;186:19-28. https://doi.org/10.1016/S0304-3835(02)00285-9
  22. Wargovich MJ, Jimenez A, McKee K, Steele VE, Velasco M, Woods J, Price R, Gray K, Kelloff GJ. Efficacy of potential chemopreventive agents on rat colon aberrant crypt formation and progression. Carcinogenesis 2000;21:1149-55. https://doi.org/10.1093/carcin/21.6.1149
  23. Li H, Kramer PM, Lubet RA, Steele VE, Kelloff GJ, Pereira MA. Effect of calcium on azoxymethane-induced aberrant crypt foci and cell proliferation in the colon of rats. Cancer Lett 1998;124:39-46. https://doi.org/10.1016/S0304-3835(97)00453-9
  24. Nelson RL, Tanure JC, Andrianopoulos G. The effect of dietary milk and calcium on experimental colorectal carcinogenesis. Dis Colon Rectum 1987;30:947-9. https://doi.org/10.1007/BF02554282
  25. Sitrin MD, Halline AG, Abrahams C, Brasitus TA. Dietary calcium and vitamin D modulate 1,2-dimethylhydrazine-induced colonic carcinogenesis in the rat. Cancer Res 1991;51:5608-13.
  26. Beaty MM, Lee EY, Glauert HP. Influence of dietary calcium and vitamin D on colon epithelial cell proliferation and 1,2-dimethylhydrazine-induced colon carcinogenesis in rats fed high fat diets. J Nutr 1993;123:144-52.
  27. Pence BC, Dunn DM, Zhao C, Patel V, Hunter S, Landers M. Protective effects of calcium from nonfat dried milk against colon carcinogenesis in rats. Nutr Cancer 1996;25:35-45. https://doi.org/10.1080/01635589609514426
  28. Huerta S, Irwin RW, Heber D, Go VL, Moatamed F, Huerta S, Ou C, Harris DM. Intestinal polyp formation in the Apcmin mouse: effects of levels of dietary calcium and altered vitamin D homeostasis. Dig Dis Sci 2003;48:870-6. https://doi.org/10.1023/A:1023083025595
  29. Ding S, McEntee MF, Whelan J, Zemel M. Adiposity-related protection of intestinal tumorigenesis: interaction with dietary calcium. Nutr Cancer 2007;58:153-61. https://doi.org/10.1080/01635580701328248
  30. Newmark HL, Yang K, Lipkin M, Kopelovich L, Liu Y, Fan K, Shinozaki H. A Western-style diet induces benign and malignant neoplasms in the colon of normal C57Bl/6 mice. Carcinogenesis 2001;22:1871-5. https://doi.org/10.1093/carcin/22.11.1871
  31. Newmark HL, Yang K, Kurihara N, Fan K, Augenlicht LH, Lipkin M. Western-style diet-induced colonic tumors and their modulation by calcium and vitamin D in C57Bl/6 mice: a preclinical model for human sporadic colon cancer. Carcinogenesis 2009;30:88-92.
  32. Liu Y, Ju J, Xiao H, Simi B, Hao X, Reddy BS, Huang MT, Newmark H, Yang CS. Effects of combination of calcium and aspirin on azoxymethane-induced aberrant crypt foci formation in the colons of mice and rats. Nutr Cancer 2008;60:660-5. https://doi.org/10.1080/01635580802290215
  33. Van Aken E, De Wever O, Correia da Rocha AS, Mareel M. Defective E-cadherin/catenin complexes in human cancer. Virchows Arch 2001;439:725-51.
  34. Hao X, Frayling IM, Willcocks TC, Han W, Tomlinson IP, Pignatelli MN, Pretlow TP, Talbot IC. Beta-catenin expression and allelic loss at APC in sporadic colorectal carcinogenesis. Virchows Arch 2002;440:362-6. https://doi.org/10.1007/s00428-001-0570-0
  35. Hao X, Palazzo JP, Ilyas M, Tomlinson I, Talbot IC. Reduced expression of molecules of the cadherin/catenin complex in the transition from colorectal adenoma to carcinoma. Anticancer Res 1997;17:2241-7.
  36. Bhagavathula N, Hanosh AW, Nerusu KC, Appelman H, Chakrabarty S, Varani J. Regulation of E-cadherin and beta-catenin by Ca2+ in colon carcinoma is dependent on calcium-sensing receptor expression and function. Int J Cancer 2007;121:1455-62. https://doi.org/10.1002/ijc.22858
  37. Tu CL, Chang W, Xie Z, Bikle DD. Inactivation of the calcium sensing receptor inhibits E-cadherin-mediated cell-cell adhesion and calcium-induced differentiation in human epidermal keratinocytes. J Biol Chem 2008;283:3519-28.
  38. Chakrabarty S, Radjendirane V, Appelman H, Varani J. Extracellular calcium and calcium sensing receptor function in human colon carcinomas: promotion of E-cadherin expression and suppression of beta-catenin/TCF activation. Cancer Res 2003;63:67-71.
  39. Shtutman M, Levina E, Ohouo P, Baig M, Roninson IB. Cell adhesion molecule L1 disrupts E-cadherin-containing adherens junctions and increases scattering and motility of MCF7 breast carcinoma cells. Cancer Res 2006;66:11370-80. https://doi.org/10.1158/0008-5472.CAN-06-2106
  40. Boivin GP, Washington K, Yang K, Ward JM, Pretlow TP, Russell R, Besselsen DG, Godfrey VL, Doetschman T, Dove WF, Pitot HC, Halberg RB, Itzkowitz SH, Groden J, Coffey RJ. Pathology of mouse models of intestinal cancer: consensus report and recommendations. Gastroenterology 2003;124:762-77. https://doi.org/10.1053/gast.2003.50094
  41. Miyoshi Y, Nagase H, Ando H, Horii A, Ichii S, Nakatsuru S, Aoki T, Miki Y, Mori T, Nakamura Y. Somatic mutations of the APC gene in colorectal tumors: mutation cluster region in the APC gene. Hum Mol Genet 1992;1:229-33. https://doi.org/10.1093/hmg/1.4.229
  42. Corpet DE, Pierre F. Point: From animal models to prevention of colon cancer. Systematic review of chemoprevention in min mice and choice of the model system. Cancer Epidemiol Biomarkers Prev 2003;12:391-400.
  43. Ju J, Hong J, Zhou JN, Pan Z, Bose M, Liao J, Yang GY, Liu YY, Hou Z, Lin Y, Ma J, Shih WJ, Carothers AM, Yang CS. Inhibition of intestinal tumorigenesis in Apcmin/+ mice by (-)-epigallocatechin-3-gallate, the major catechin in green tea. Cancer Res 2005;65:10623-31. https://doi.org/10.1158/0008-5472.CAN-05-1949
  44. Sang S, Ju J, Lambert JD, Lin Y, Hong J, Bose M, Wang S, Bai N, He K, Reddy BS, Ho CT, Li F, Yang CS. Wheat bran oil and its fractions inhibit human colon cancer cell growth and intestinal tumorigenesis in Apc(min/+) mice. J Agric Food Chem 2006;54:9792-7. https://doi.org/10.1021/jf0620665
  45. Hao X, Sun Y, Yang CS, Bose M, Lambert JD, Ju J, Lu G, Lee MJ, Park S, Husain A, Wang S. Inhibition of intestinal tumorigenesis in Apc(min/+) mice by green tea polyphenols (polyphenon E) and individual catechins. Nutr Cancer 2007;59:62-9. https://doi.org/10.1080/01635580701365050
  46. Carafoli E. Intracellular calcium homeostasis. Annu Rev Biochem 1987;56:395-433. https://doi.org/10.1146/annurev.bi.56.070187.002143
  47. Newmark HL, Heaney RP, Lachance PA. Should calcium and vitamin D be added to the current enrichment program for cereal-grain products? Am J Clin Nutr 2004;80:264-70.
  48. Newmark HL. Nutrient density: an important and useful tool for laboratory animal studies. Carcinogenesis 1987;8:871-3. https://doi.org/10.1093/carcin/8.7.871
  49. Standing Committee on the Scientific Evaluation of Dietary Reference Intakes, Food and Nutrition Board, Institute of Medicine. Dietary Reference Intakes for Calcium, Phosphorus, Magnesium, Vitamin D, and Fluoride. Washington, D.C: National Academy Press; 1997.

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