References
- Shen Y, Zhang H, Cheng L, Wang L, Qian H, Qi X (2016) In vitro and in vivo antioxidant activity of polyphenols extracted from black highland barley. Food Chem, 194, 1003-1012 https://doi.org/10.1016/j.foodchem.2015.08.083
- Niki E (2016) Antioxidant capacity of foods for scavenging reactive oxidants and inhibition of plasma lipid oxidation induced by multiple oxidants. Food Funct, 7, 2156-2168 https://doi.org/10.1039/C6FO00275G
- Maes M, Twisk FNM (2010) Chronic fatigue syndrome: Harvey and Wessely's (bio) psychosocial model versus a bio (psychosocial) model based on inflammatory and oxidative and nitrosative stress pathways. BMC Medicine, 8, 1-13 https://doi.org/10.1186/1741-7015-8-1
- Rittie L, Fisher GJ (2002) UV-light-induced signal cascades and skin aging. Ageing Res Rev, 1, 705-720 https://doi.org/10.1016/S1568-1637(02)00024-7
- Shen S, Callaghan D, Juzwik C, Xiong H, Huang P, Zhang W (2014) ABCG2 reduces ROS-mediated toxicity and inflammation: a potential role in Alzheimer's disease. J Neurochem, 114, 1590-1604
- Lee JH, Shin YJ, Cho DJ, Lim HJ, Choi WE, Lee YK (2004) Antitumor and antimutagenic effect of the proteinpolysaccharides from Poluporus umbellatus. J Korean Soc Food Sci Nutr, 33, 475-479 https://doi.org/10.3746/jkfn.2004.33.3.475
- Park MS, So JS, Bahk GJ (2015) Antioxidative and anticancer activities of water extracts from different parts of Taraxacum coreanum Nakai cultivated in Korea. J Korean Soc Food Sci Nutr, 44, 1234-1240 https://doi.org/10.3746/jkfn.2015.44.8.1234
- Burks DA, Littleton RH (1992) The epidemiology of prostate cancer in black men. Henry Ford Hosp Med J, 40, 89-92
- Panov A, Orynbayeva Z (2013) Bioenergetic and antiapoptotic properties of mitochondria from cultured human prostate cancer cell lines PC-3, DU145 and LNCaP. PLoS One, 8, e72078 https://doi.org/10.1371/journal.pone.0072078
- Won YS, Lee JH, Kwon SJ, Ahn DU, Shin DY, Seo KI (2014) Anticancer effects of cultivated Orostachys japonicus on human prostate cancer cells. J Korean Soc Food Sci Nutr, 43, 67-73 https://doi.org/10.3746/jkfn.2014.43.1.067
- Kwon SH, Kwon SJ, Kim JY, Park KW, Shim KH, Seo KI (2009) Protective effect of Corni fructus ethanol extracts against environmental hormones in human prostate cancer cells. J Korean Soc Food Sci Nutr, 38, 663-666 https://doi.org/10.3746/jkfn.2009.38.6.663
- Park SY, Kim EJ, Lim DY, Kim JS, Lim SS, Shin HK, Yoon JH (2008) Inhibitory effect of the hexane extract of Saussurea lappa on the growth of LNCaP human prostate cancer cells. J Korean Soc Food Sci Nutr, 37, 8-15 https://doi.org/10.3746/jkfn.2008.37.1.8
- Hwang EJ, Cha YJ, Park MH, Lee JW, Lee SY (2004) Cytotoxicity and chemosensitizing effect of camellia (Camellia japonica) tea extracts. J Korean Soc Food Sci Nutr, 33, 487-493 https://doi.org/10.3746/jkfn.2004.33.3.487
- Kwak CS, Lim SJ, Kim SA, Park SC, Lee MS (2004) Antioxidative and antimutagenic effects of Korean buckwheat, sorghum, millet and Job's tears. J Korean Soc Food Sci Nutr, 33, 921-929 https://doi.org/10.3746/jkfn.2004.33.6.921
- Ha YD, Lee SP (2001) Characteristics of proteins in Italian millet, sorghum and common meillet. Korean J Postharvest Sci Technol, 8, 187-192
- An TK (1999) Illustrated book of Korean medicinal herbs. Kyohak Publishing Co Ltd, Seoul, Korea, p 887
- Zhang L, Liu R, Niu W (2014) Phytochemical and antiproliferative activity of proso millet. PLoS One, 9, e104058 https://doi.org/10.1371/journal.pone.0104058
- Park MY, Seo DW, Lee JY, Sung MK, Lee YM, Jang HH, Choi HY, Kim JH, Park DS (2011) Effects of Panicum miliaceum L. extract on adipogenic transcription factors and fatty acid accumulation in 3T3-L1 adipocytes. Nutr Res Pract, 5, 192-197 https://doi.org/10.4162/nrp.2011.5.3.192
- Park MY, Jang HH, Kim JB, Yoon HN, Lee JY, Lee YM, Kim JH, Park DS (2011) Hog millet (Panicum miliaceum L.)-supplemented diet ameliorates hyperlipidemia and hepatic lipid accumulation in C57BL/6J-ob/ob mice. Nutr Res Pract, 5, 511-519 https://doi.org/10.4162/nrp.2011.5.6.511
- Kim KO, Kim HS, Ryu HS (2006) Effect of Sorghum bicolor L. Moench(Sorghum, su-su) water extracts on mouse immune cell activation. J Korean Diet Assoc, 12, 82-88
- Vermont PD, Pangloli P, Jones L, McClureb A, Patel A (2016) Phytochemical concentrations and biological activities of Sorghum bicolor alcoholic extracts. Food Funct, 7, 3410-3420 https://doi.org/10.1039/C6FO00757K
-
Park JH, Lee SH, Chung IM, Park YS (2012) Sorghum extract exerts an anti-diabetic effect by improving insulin sensitivity via
$PPAR-{\gamma}$ in mice fed a high-fat diet. Nutr Res Pract, 6, 322-327 https://doi.org/10.4162/nrp.2012.6.4.322 - Gao X, Bjork L, Trajkovski V, Uggla M (2000) Evaluation of antioxidant activities of rosehip ethanol extracts in different test systems. J Sci Food Agric, 80, 2021-2027 https://doi.org/10.1002/1097-0010(200011)80:14<2021::AID-JSFA745>3.0.CO;2-2
- Blois MS (1958) Antioxidant determination by the use of a stable free radical. Nature, 181, 1199-1200 https://doi.org/10.1038/1811199a0
- Biglari F, AlKarkhi AFM, Easa AM (2008) Antioxidant activity and phenolic content of various date palm (Phoenix dactylifera) fruits from Iran. Food Chem, 107, 1636-1641 https://doi.org/10.1016/j.foodchem.2007.10.033
- Yildirim A, Mavi A, Kara AA (2001) Determination of antioxidant and antimicrobial activities of Rumex crispus L. extracts. J Agric Food Chem, 49, 4083-4089 https://doi.org/10.1021/jf0103572
- Marklund S, Marklund G (1974) Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem, 47, 469-474 https://doi.org/10.1111/j.1432-1033.1974.tb03714.x
- Vichai V, Kirtikara K (2006) Sulforhodamine B colorimetric assay for cytotoxicity screening. Nature Protocols, 1, 1112-1116 https://doi.org/10.1038/nprot.2006.179
- Kang HI, Kim JY, Kwon SJ, Park KW, Kang JS, Seo KI (2010) Antioxidative effects of peanut sprout extracts. J Korean Soc Food Sci Nutr, 39, 941-946 https://doi.org/10.3746/jkfn.2010.39.7.941
-
Kim DG, Lee BG, Kim HY (2003) Use of Fraxnius rhynchophylla
$H{\cdot}$ ance bark as antioxidant. J Kor For En, 22, 69-76 - Kang SR, Shin MO, Kim SG, Lee SH, Kim MH (2009) Antioxidative activity of pine (Pinus densiflora) needle extracts in rats fed high-cholesterol diet. J Korean Soc Food Sci Nutr, 38, 423-429 https://doi.org/10.3746/jkfn.2009.38.4.423
- Lee JM, Chung H, Chang PS, Lee JH (2007) Development of a method predicting the oxidative stability of edible oils using 2,2-diphenyl-1- picrylhydrazyl (DPPH). Food Chem, 103, 662-669 https://doi.org/10.1016/j.foodchem.2006.07.052
- Berg RVD, Haenen GRMM, Berg HVD, Bast A (1999) Applicability of an improved Trolox equivalent antioxidant capacity (TEAC) assay for evaluation of antioxidant capacity measurements of mixtures. Food Chem, 66, 511-517 https://doi.org/10.1016/S0308-8146(99)00089-8
- Ko JY, Song SB, Lee JS, Kang JR, Seo MC, Oh BG, Kwak DY, Nam MH, Jeong HS, Woo KS (2011) Changes in chemical components of foxtail millet, proso millet, and sorghum with germination. J Korean Soc Food Sci Nutr, 40, 1128-1135 https://doi.org/10.3746/jkfn.2011.40.8.1128
- Oh YN, Jin SJ, Park HJ, Kwon HJ, Kim BW (2014) Anti-oxidative and anti-cancer activities by cell cycle regulation of Salsola collina extract. Korean J Microbiol Biotechnol, 42, 73-81 https://doi.org/10.4014/kjmb.1311.11009
- Khandrika L, Kumar B, Koul S, Maroni P, Koul HK (2009) Role of oxidative stress in prostate cancer. Cancer Lett, 282, 125-136 https://doi.org/10.1016/j.canlet.2008.12.011
- Liu C, Zhu Y, Lou W, Nadiminty N, Chen X, Zhou Q, Shi XB, White RW, Gao AC (2013) Functional p53 determines Docetaxel sensitivity in prostate cancer cells. The Prostate, 73, 418-427 https://doi.org/10.1002/pros.22583
- Wyllie AH, Kerr JFR, Currie AR, (1980) Cell death: the significance of apoptosis. Int Rev Cytol, 68, 251-306 https://doi.org/10.1016/S0074-7696(08)62312-8
- Fulda S, Debatin KM (2006) Extrinsic versus intrinsic apoptosis pathways in anticancer chemotherapy. Oncogene, 25, 4798-4811 https://doi.org/10.1038/sj.onc.1209608
-
Suganyadevi P, Saravanakumar KM, Mohandas S (2013) The antiproliferative activity of 3-deoxyanthocyanins extracted from red sorghum (Sorghum bicolor) bran through
$p^{53}$ -dependent and Bcl-2 gene expression in breast cancer cell line. Life Sci, 92, 379-382 https://doi.org/10.1016/j.lfs.2013.01.006 - Park JH, Darvin P, Lim EJ, Joung YH, Hong DY, Park EU, Park SH, Choi SK, Moon ES, Cho BW, Park KD, Lee HK, Kim MJ, Park DS, Chung IM, Yang YM (2012) Hwanggeumchal sorghum induces cell cycle arrest, and suppresses tumor growth and metastasis through Jak2/STAT pathways in breast cancer xenografts. PLoS One, 7, e40531 https://doi.org/10.1371/journal.pone.0040531
- Azuma K, Nakayama M, Koshioka M, Ippoushi K, Yamaguchi Y, Kohata K, Yamauchi Y, Ito H, Higashio H (1999) Phenolic antioxidants from the leaves of Corchorus olitorius L.. J Agric Food Chem, 47, 3963-3966 https://doi.org/10.1021/jf990347p
- Senter SD, Horvat RJ, Forbus WR (1983) Comparative GLC-MS analysis of phenolic acids of selected tree nuts. J Food Sci, 48, 798-799 https://doi.org/10.1111/j.1365-2621.1983.tb14902.x
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