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Inhibition of MMP-2 and MMP-9 activities by solvent-partitioned Sargassum horneri extracts

  • Karadeniz, Fatih (Department of Organic Material Science and Engineering, Pusan National University) ;
  • Lee, Seul-Gi (Department of Food and Nutrition, College of Medical and Life Sciences, Silla University) ;
  • Oh, Jung Hwan (Department of Food and Nutrition, College of Medical and Life Sciences, Silla University) ;
  • Kim, Jung-Ae (Department of Food and Nutrition, College of Medical and Life Sciences, Silla University) ;
  • Kong, Chang-Suk (Department of Food and Nutrition, College of Medical and Life Sciences, Silla University)
  • Received : 2018.01.18
  • Accepted : 2018.03.12
  • Published : 2018.06.30

Abstract

Background: Matrix metalloproteinases (MMPs) are linked with several complications such as metastasis of cancer progression, oxidative stress, and hepatic fibrosis. Brown seaweeds are being extensively studied for their bioactive molecule content against cancer progression. In this context, Sargassum horneri was reported to possess various bioactivities including antiviral, antimicrobial, and anti-inflammatory partly due to its phenolic compound content. Methods: In this study, potential of S. horneri was evaluated through anti-MMP effect in HT1080 fibrosarcoma cells. S. horneri crude extract was fractionated with organic solvents, namely, water ($H_2O$), n-buthanol (n-BuOH), 85% aqueous methanol (85% aq. MeOH), and n-hexane. The non-toxicity of fraction samples (Sargassum horneri solvent-partitioned extracts (SHEs)) was confirmed by cell-viability assay. SHEs were tested for their ability to inhibit MMP enzymatic activity through gelatin digestion evaluation and cell migration assay. Expressions of MMP-2 and MMP-9 and tissue inhibitors of MMP (TIMPs) were evaluated by reverse transcription and Western blotting. Results: All fractions inhibited the enzymatic activities of MMP-2 and MMP-9 according to gelatin zymography. Except $H_2O$ fraction, fractions hindered the cell migration significantly. All tested fractions suppressed both mRNA and protein levels of MMP-2, MMP-9, TIMP-1, and TIMP-2. Conclusion: Overall, current results suggested that S. horneri has potential to be a good source for anti-MMP agents, and further investigations are underway for better understanding of the action mechanism and isolation and elucidation of the bioactive molecules.

Keywords

References

  1. Bauvois B. New facets of matrix metalloproteinases MMP-2 and MMP-9 as cell surface transducers: outside-in signaling and relationship to tumor progression. Biochim Biophys Acta Rev Cancer. 2012;1825:29-36. https://doi.org/10.1016/j.bbcan.2011.10.001
  2. Benjamin MM, Khalil RA. Matrix metalloproteinase inhibitors as investigative tools in the pathogenesis and management of vascular disease. EXS. 2012;103: 209-79.
  3. Bhatnagar I, Kim SK. Marine antitumor drugs: status, shortfalls and strategies. Mar Drugs. 2010;8:2702-20. https://doi.org/10.3390/md8102702
  4. de la Mare JA, Lawson JC, Chiwakata MT, Beukes DR, Edkins AL, Blatch GL. Quinones and halogenated monoterpenes of algal origin show antiproliferative effects against breast cancer cells in vitro. Investig New Drugs. 2012;30:2187-200. https://doi.org/10.1007/s10637-011-9788-0
  5. Egeblad M, Werb Z. New functions for the matrix metalloproteinases in cancer progression. Nat Rev Cancer. 2002;2:161-74. https://doi.org/10.1038/nrc745
  6. Holdt SL, Kraan S. Bioactive compounds in seaweed: functional food applications and legislation. J Appl Phycol. 2011;23:543-97. https://doi.org/10.1007/s10811-010-9632-5
  7. Ibanez E, Cifuentes A. Benefits of using algae as natural sources of functional ingredients. J Sci Food Agric. 2013;93:703-9. https://doi.org/10.1002/jsfa.6023
  8. Jiao J, Friedman SL, Aloman C. Hepatic fibrosis. Curr Opin Gastroenterol. 2009;25: 223-9. https://doi.org/10.1097/MOG.0b013e3283279668
  9. Jones JL, Walker RA. Control of matrix metalloproteinase activity in cancer. J Pathol. 1997;183:377-9. https://doi.org/10.1002/(SICI)1096-9896(199712)183:4<377::AID-PATH951>3.0.CO;2-R
  10. Kato H, Duarte S, Liu D, Busuttil RW, Coito AJ. Matrix metalloproteinase-2 (MMP-2) gene deletion enhances MMP-9 activity, impairs PARP-1 degradation, and exacerbates hepatic ischemia and reperfusion injury in mice. PLoS One. 2015; 10(9):e0137642. https://doi.org/10.1371/journal.pone.0137642
  11. Kim YA, Kong CS, Park HH, Lee E, Jang MS, Nam KH, Seo Y. Anti-inflammatory activity of heterocarpin from the salt marsh plant Corydalis heterocarpa in LPS-induced RAW 264.7 macrophage cells. Molecules. 2015;20:14474-86. https://doi.org/10.3390/molecules200814474
  12. Matanjun P, Mohamed S, Mustapha NM, Muhammad K. Nutrient content of tropical edible seaweeds, Eucheuma cottonii, Caulerpa lentillifera and Sargassum polycystum. J Appl Phycol. 2009;21:75-80. https://doi.org/10.1007/s10811-008-9326-4
  13. Moss LAS, Jensen-Taubman S, Stetler-Stevenson WG. Matrix metalloproteinases: changing roles in tumor progression and metastasis. Am J Pathol. 2012;181: 1895-9. https://doi.org/10.1016/j.ajpath.2012.08.044
  14. Overall CM, Lopez-Otin C. Strategies for MMP inhibition in cancer: innovations for the post-trial era. Nat Rev Cancer. 2002;2:657-72. https://doi.org/10.1038/nrc884
  15. Patarra RF, Paiva L, Neto AI, Lima E, Baptista J. Nutritional value of selected macroalgae. J Appl Phycol. 2011;23:205-8. https://doi.org/10.1007/s10811-010-9556-0
  16. Plaza M, Santoyo S, Jaime L, Reina GGB, Herrero M, Senorans FJ. Screening for bioactive compounds from algae. J Pharm Biomed Anal. 2010;51:450-5. https://doi.org/10.1016/j.jpba.2009.03.016
  17. Reuter S, Gupta SC, Chaturvedi MM, Aggarwal BB. Oxidative stress, inflammation, and cancer: how are they linked? Free Radic Biol Med. 2010;49:1603-16. https://doi.org/10.1016/j.freeradbiomed.2010.09.006
  18. Seo Y, Lee HJ, Park KE, Kim YA, Ahn JW, Yoo JS, Lee BJ. Peroxynitrite-scavenging constituents from the brown alga Sargassum thunbergii. Biotechnol Bioprocess Eng. 2004;9:212-6. https://doi.org/10.1007/BF02942295
  19. Shipeng Y, Woo HC, Choi JH, Park YB, Chun BS. Measurement of antioxidant activities and phenolic and flavonoid contents of the brown seaweed Sargassum horneri: comparison of supercritical $CO_2$ and various solvent extractions. Fish Aquat Sci. 2015;18:123-30.
  20. Thomas NV, Kim SK. Potential pharmacological applications of polyphenolic derivatives from marine brown algae. Environ Toxicol Pharmacol. 2011;32: 325-35. https://doi.org/10.1016/j.etap.2011.09.004
  21. Tu G, Xu W, Huang H, Li S. Progress in the development of matrix metalloproteinase inhibitors. Curr Med Chem. 2008;15:1388-95. https://doi.org/10.2174/092986708784567680
  22. Yu P, Gu H. Bioactive substances from marine fishes, shrimps and algae and their functions: present and future. Crit Rev Food Sci Nutr. 2015;55:1114-36. https://doi.org/10.1080/10408398.2012.686933

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