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$\beta$-Glucan enhanced apoptosis in human colon cancer cells SNU-C4

  • Kim, Mi-Ja (Department of Food and Nutrition, Dongduk Women's University) ;
  • Hong, Se-Young (Department of Food and Nutrition, Dongduk Women's University) ;
  • Kim, Sun-Kyu (Department of Fermented Food Science, Seoul university of Venture & Information) ;
  • Cheong, Chul (Department of Fermented Food Science, Seoul university of Venture & Information) ;
  • Park, Hong-Ju (Department of Agrofood Resources, National Academy of Agricultural Science, RDA) ;
  • Chun, Hye-Kyung (Department of Agrofood Resources, National Academy of Agricultural Science, RDA) ;
  • Jang, Ki-Hyo (Department of Food and Nutrition, Kangwon National University) ;
  • Yoon, Byung-Dae (Molecular Bioprocess Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Kim, Chul-Ho (Molecular Bioprocess Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Kang, Soon-Ah (Department of Fermented Food Science, Seoul university of Venture & Information)
  • Published : 2009.09.30

Abstract

The apoptotic effect of bacteria-derived $\beta$-glucan was investigated in human colon cancer cells SNU-C4 using terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end labeling (TUNEL) assay, reverse transcription-polymerase chain reaction (RT-PCR) expressions of Bcl-2, Bax, and Caspase-3 genes, and assay of caspase-3 enzyme activity. $\beta$-Glucan of 10, 50, and $100{\mu}g$/mL decreased cell viability in a dose-dependent manner with typical apoptotic characteristics, such as morphological changes of chromatin condensation and apoptotic body formation from TUNEL assay. In addition, $\beta$-glucan ($100{\mu}g$/mL) decreased the expression of Bc1-2 by 0.6 times, whereas the expression of Bax and Caspase-3 were increased by 3.1 and 2.3 times, respectively, compared to untreated control group. Furthermore, the caspase-3 activity in the $\beta$-glucan-treated group was significantly increased compared to those in control group (P < 0.05). Bacterial derived $\beta$-glucan could be used as an effective compound inducing apoptosis in human colon cancer.

Keywords

References

  1. Behall K M, Scholfield DJ & Hallfrisch J (1997). Effect of $\beta$-glucan level in oat fiber extracts on blood lipids in men and women. J Am Coll Nutr 16:46-51 https://doi.org/10.1080/07315724.1997.10718648
  2. Cohen JJ (1993). Apoptosis. Immunol Today 14:126-130 https://doi.org/10.1016/0167-5699(93)90214-6
  3. Davidson MH, Dugan LD, Burns JH, Bova J, Story K & Drennan KB (1991). The ypocholesterolemic effects of β-glucan in oatmeal and oat bran: a dose-controlled study. J Am Med Assoc 265:1833-1839 https://doi.org/10.1001/jama.265.14.1833
  4. Harlozinska A (2005). Progress in molecular mechanisms of tumor metastasis and angiogenesis. Anticancer Res 25:3327-3333
  5. Hong KH, Jang KH, Lee JC, Kim SH, Kim MK, Lee IY, Kim SM, Lim YH & Kang SA (2005). Bacterial β-glucan exhibits potent hypoglycemic activity via decrease of serum lipids and adiposity, and increase of UCP mRNA expression. J Microbiol Biotechnol 15:823-830
  6. Kobayashi H, Yoshida R, Kanada Y, Fukuda Y, Yagyu T, Inagaki K, Kondo T, Kurita N, Suzuki M, Kanayama N & Terao T (2005). Suppressing effects of daily oral supplementation of β-glucan extracted from Agaricus blazei Murill on spontaneous and peritoneal disseminated metastasis in mouse model. J Cancer Res Clin Oncol 131:527-538 https://doi.org/10.1007/s00432-005-0672-1
  7. McIntosh GH, Whyte J, McArthur R & Nestel PJ (1991). Barley and wheat foods: influence on plasma cholesterol concentrations in hypercholesterolemic men. Am J Clin Nutr 53:1205-1209 https://doi.org/10.1093/ajcn/53.5.1205
  8. Moudy AM, Handran SD, Goldberg MP, Ruffin N, Karl I, Kranz-Eble P, DeVivo DC & Rothman SM (1995). Abnormal calcium homeostasis and mitochondrial polarization in a human encephalomyopathy. Proc Natl Acad Sci U S A 92:729-733 https://doi.org/10.1073/pnas.92.3.729
  9. Nameda S, Miura NN, Adachi Y & Ohno N (2007). Antibiotics protect against septic shock in mice administered β-glucan and indomethacin. Microbiol Immunol 51:851-859 https://doi.org/10.1111/j.1348-0421.2007.tb03981.x
  10. Newman RK, Lewis SE, Newman CW, Bioik RJ & Ramage RT (1989). Hypocholesterolemic effects of barley food on healthy men. Nutr Rep Int 34:749-760
  11. Nicolosi R, Bell SJ, Bistrian BR, Greenberg I, Forse RA & Blackburn GL (1999). Plasma lipid changes after supplementation with $\beta$-glucan fiber from yeast. Am J Clin Nutr 70:208-212 https://doi.org/10.1093/ajcn.70.2.208
  12. Novak M & Vetvicka V (2008). Β-glucans, history, and the present: immunomodulatory aspects and mechanisms of action. J Immunotoxicol 5:47-57 https://doi.org/10.1080/15476910802019045
  13. Ohno N, Egawa Y, Hashimoto T, Adachi Y & Yadomae T (1996). Effect of -$\beta$glucans on the nitric oxide synthesis by peritoneal macrophage in mice. Biol Pharm Bull 19:608-612 https://doi.org/10.1248/bpb.19.608
  14. Oltvai ZN, Milliman CL & Korsmeyer SJ (1993). Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death. Cell 74:609-619 https://doi.org/10.1016/0092-8674(93)90509-O
  15. Park HJ, Kim MJ, Ha E & Chung JH (2008). Apoptotic effect of hesperidin through caspase3 activation in human colon cancer cells, SNU-C4. Phytomedicine 15:147-151 https://doi.org/10.1016/j.phymed.2007.07.061
  16. Qiao L, Hanif R, Sphicas E, Shiff SJ & Rigas B (1998). Effect of aspirin on induction of apoptosis in HT-29 human colon adenocarcinoma cells. Biochem Pharmacol 55:53-64 https://doi.org/10.1016/S0006-2952(97)00400-0
  17. Siripong P, Hahnvajanawong C, Yahuafai J, Piyaviriyakul S, Kanokmedhakul K, Kongkathip N, Ruchirawat S & Oku N (2009) Induction of Apoptosis by Rhinacanthone isolated from Rhinacanthus nasutus roots in human cervical carcinoma cells. Biol Pharm Bull 32:1251-1260 https://doi.org/10.1248/bpb.32.1251
  18. Smiley ST, Reers M, Mottola-Hartshorn C, Lin M, Chen A, Smith TW, Steele GD Jr & Chen LB (1991). Intracellular heterogeneity in mitochondrial membrane potentials revealed by a J-aggregateforming lipophilic cation JC-1. Proc Natl Acad Sci U S A 88:3671-3675 https://doi.org/10.1073/pnas.88.9.3671
  19. Volman JJ, Ramakers JD & Plat J (2008). Dietary modulation of immune function by $\beta$-glucans. Physiol Behav 94:276-284 https://doi.org/10.1016/j.physbeh.2007.11.045
  20. Yamamoto K, Kimura T, Sugitachi A & Matsuura N (2009). Anti-angiogenic and anti-metastatic effects of $\beta$-1,3-D-glucan purified from Hanabiratake, Sparassis crispa. Biol Pharm Bull 32:259-263 https://doi.org/10.1248/bpb.32.259
  21. Yang ZG, Chen AQ & Liu B (2009). Antiproliferation and apoptosis induced by evodiamine in human colorectal carcinoma cells (COLO-205). Chem Biodivers 6:924-933 https://doi.org/10.1002/cbdv.200800256

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