참고문헌
- Taji S, Yamada T, In Y, Wada SI, Usami Y, Sakuma K, Tanaka R. Three new lanostane triterpenoids from Inonotus obliquus. Helv Chim Acta 2007;90:2047-57. https://doi.org/10.1002/hlca.200790214
- Saar M. Fungi in khanty folk medicine. J Ethnopharmacol 1991;31: 175-9. https://doi.org/10.1016/0378-8741(91)90003-V
- Zhao F, Piao H, Han C. Studies on anti-mutation active constituents of the Fuscoporia oblique. J Med Sci Yanbian Univ 2004;27:250-2.
- Chen H, Xu X, Zhu Y. Optimization of hydroxyl radical scavenging activity of exo-polysaccharides from Inonotus obliquus in submerged fermentation using response surface methodology. J Microbiol Biotechnol 2010;20:835-43.
- Choi SY, Hur SJ, An CS, Jeon YH, Jeoung YJ, Bak JP, Lim BO. Anti-inflammatory effects of Inonotus obliquus in colitis induced by dextran sodium sulfate. J Biomed Biotechnol 2010;2010:943516.
- Kahlos K, Kangas L, Hiltunen R. Antitumor activity of some compounds and fractions from an n-hexane extract of Inonotus obliquus in vitro. Acta Pharm Fennica 1987;96:33-40
- Ichimura T, Watanabe O, Maruyama S. Inhibition of HIV-1 protease by water-soluble lignin-like substance from an edible mushroom, Fuscoporia obliqua. Biosci Biotechnol Biochem 1998;62:575-7. https://doi.org/10.1271/bbb.62.575
- Nakata T, Yamada T, Taji S, Ohishi H, Wada S, Tokuda H, Sakuma K, Tanaka R. Structure determination of inonotsuoxides A and B and in vivo anti-tumor promoting activity of inotodiol from the sclerotia of Inonotus obliquus. Bioorg Med Chem 2007;15:257-64. https://doi.org/10.1016/j.bmc.2006.09.064
- Shibnev VA, Mishin DV, Garaev TM, Finogenova NP, Botikov AG, Deryabin PG. Antiviral activity of Inonotus obliquus fungus extract towards infection caused by hepatitis C virus in cell cultures. Bull Exp Biol Med 2011;151:612-4. https://doi.org/10.1007/s10517-011-1395-8
- Song FQ, Liu Y, Kong XS, Chang W, Song G. Progress on understanding the anticancer mechanisms of medicinal mushroom: inonotus obliquus. Asian Pac J Cancer Prev 2013;14:1571-8. https://doi.org/10.7314/APJCP.2013.14.3.1571
- Lee SH, Hwang HS, Yun JW. Antitumor activity of water extract of a mushroom, Inonotus obliquus, against HT-29 human colon cancer cells. Phytother Res 2009;23:1784-9. https://doi.org/10.1002/ptr.2836
- Lee IK, Kim YS, Jang YW, Jung JY, Yun BS. New antioxidant polyphenols from the medicinal mushroom Inonotus obliquus. Bioorg Med Chem Lett 2007;17:6678-81. https://doi.org/10.1016/j.bmcl.2007.10.072
- Park YM, Won JH, Kim YH, Choi JW, Park HJ, Lee KT. In vivo and in vitro anti-inflammatory and anti-nociceptive effects of the methanol extract of Inonotus obliquus. J Ethnopharmacol 2005; 101:120-8. https://doi.org/10.1016/j.jep.2005.04.003
- Nakajima Y, Sato Y, Konishi T. Antioxidant small phenolic ingredients in Inonotus obliquus (persoon) Pilat (Chaga). Chem Pharm Bull (Tokyo) 2007;55:1222-6. https://doi.org/10.1248/cpb.55.1222
- Youn MJ, Kim JK, Park SY, Kim Y, Kim SJ, Lee JS, Chai KY, Kim HJ, Cui MX, So HS, Kim KY, Park R. Chaga mushroom (Inonotus obliquus) induces G0/G1 arrest and apoptosis in human hepatoma HepG2 cells. World J Gastroenterol 2008;14:511-7. https://doi.org/10.3748/wjg.14.511
- Hyun KW, Jeong SC, Lee DH, Park JS, Lee JS. Isolation and characterization of a novel platelet aggregation inhibitory peptide from the medicinal mushroom, Inonotus obliquus. Peptides 2006; 27:1173-8. https://doi.org/10.1016/j.peptides.2005.10.005
- Cui Y, Kim DS, Park KC. Antioxidant effect of Inonotus obliquus. J Ethnopharmacol 2005;96:79-85. https://doi.org/10.1016/j.jep.2004.08.037
- Ma L, Chen H, Dong P, Lu X. Anti-inflammatory and anticancer activities of extracts and compounds from the mushroom Inonotus obliquus. Food Chem 2013;139:503-8. https://doi.org/10.1016/j.foodchem.2013.01.030
- Senderowicz AM. Novel direct and indirect cyclin-dependent kinase modulators for the prevention and treatment of human neoplasms. Cancer Chemother Pharmacol 2003;52 Suppl 1:S61-73. https://doi.org/10.1007/s00280-003-0624-x
- Swanton C. Cell-cycle targeted therapies. Lancet Oncol 2004;5: 27-36. https://doi.org/10.1016/S1470-2045(03)01321-4
- Sherr CJ. Cancer cell cycles. Science 1996;274:1672-7. https://doi.org/10.1126/science.274.5293.1672
- Johnson DG, Walker CL. Cyclins and cell cycle checkpoints. Annu Rev Pharmacol Toxicol 1999;39:295-312. https://doi.org/10.1146/annurev.pharmtox.39.1.295
- Vermeulen K, Van Bockstaele DR, Berneman ZN. The cell cycle: a review of regulation, deregulation and therapeutic targets in cancer. Cell Prolif 2003;36:131-49. https://doi.org/10.1046/j.1365-2184.2003.00266.x
- Hall M, Peters G. Genetic alterations of cyclins, cyclin-dependent kinases, and Cdk inhibitors in human cancer. Adv Cancer Res 1996; 68:67-108. https://doi.org/10.1016/S0065-230X(08)60352-8
- Kim EJ, Holthuizen PE, Park HS, Ha YL, Jung KC, Park JH. Trans-10,cis-12-conjugated linoleic acid inhibits Caco-2 colon cancer cell growth. Am J Physiol Gastrointest Liver Physiol 2002;283: G357-67. https://doi.org/10.1152/ajpgi.00495.2001
- Cho HJ, Kim EJ, Lim SS, Kim MK, Sung MK, Kim JS, Park JH. Trans-10,cis-12, not cis-9,trans-11, conjugated linoleic acid inhibits G1-S progression in HT-29 human colon cancer cells. J Nutr 2006;136:893-8. https://doi.org/10.1093/jn/136.4.893
- Cho HJ, Kim WK, Kim EJ, Jung KC, Park S, Lee HS, Tyner AL, Park JH. Conjugated linoleic acid inhibits cell proliferation and ErbB3 signaling in HT-29 human colon cell line. Am J Physiol Gastrointest Liver Physiol 2003;284:G996-1005. https://doi.org/10.1152/ajpgi.00347.2002
- Kim EJ, Lim SS, Park SY, Shin HK, Kim JS, Park JH. Apoptosis of DU145 human prostate cancer cells induced by dehydrocostus lactone isolated from the root of Saussurea lappa. Food Chem Toxicol 2008;46:3651-8. https://doi.org/10.1016/j.fct.2008.08.038
- Handa N, Yamada T, Tanaka R. Four new lanostane-type triterpenoids from Inonotus obliquus. Phytochem Lett 2012;5:480-5. https://doi.org/10.1016/j.phytol.2012.04.010
- Song Y, Hui J, Kou W, Xin R, Jia F, Wang N, Hu F, Zhang H, Liu H. Identification of Inonotus obliquus and analysis of antioxidation and antitumor activities of polysaccharides. Curr Microbiol 2008; 57:454-62. https://doi.org/10.1007/s00284-008-9233-6
- Sun Y, Yin T, Chen XH, Zhang G, Curtis RB, Lu ZH, Jiang JH. In vitro antitumor activity and structure characterization of ethanol extracts from wild and cultivated Chaga medicinal mushroom, Inonotus obliquus (Pers.:Fr.) Pilat (Aphyllophoromycetideae). Int J Med Mushrooms 2011;13:121-30. https://doi.org/10.1615/IntJMedMushr.v13.i2.40
- Xiong Y, Hannon GJ, Zhang H, Casso D, Kobayashi R, Beach D. p21 is a universal inhibitor of cyclin kinases. Nature 1993;366:701-4. https://doi.org/10.1038/366701a0
- Gartel AL, Tyner AL. Transcriptional regulation of the p21(WAF1/ CIP1) gene. Exp Cell Res 1999;246:280-9. https://doi.org/10.1006/excr.1998.4319
- Chu IM, Hengst L, Slingerland JM. The Cdk inhibitor p27 in human cancer: prognostic potential and relevance to anticancer therapy. Nat Rev Cancer 2008;8:253-67. https://doi.org/10.1038/nrc2347
- Wu CL, Zukerberg LR, Ngwu C, Harlow E, Lees JA. In vivo association of E2F and DP family proteins. Mol Cell Biol 1995;15:2536-46. https://doi.org/10.1128/MCB.15.5.2536
- Das SK, Hashimoto T, Shimizu K, Yoshida T, Sakai T, Sowa Y, Komoto A, Kanazawa K. Fucoxanthin induces cell cycle arrest at G0/G1 phase in human colon carcinoma cells through up-regulation of p21 WAF1/Cip1. Biochim Biophys Acta 2005;1726:328-35. https://doi.org/10.1016/j.bbagen.2005.09.007
- Bartkova J, Gron B, Dabelsteen E, Bartek J. Cell-cycle regulatory proteins in human wound healing. Arch Oral Biol 2003;48:125-32. https://doi.org/10.1016/S0003-9969(02)00202-9
- Korenjak M, Brehm A. E2F-Rb complexes regulating transcription of genes important for differentiation and development. Curr Opin Genet Dev 2005;15:520-7. https://doi.org/10.1016/j.gde.2005.07.001
- Youn MJ, Kim JK, Park SY, Kim Y, Park C, Kim ES, Park KI, So HS, Park R. Potential anticancer properties of the water extract of Inonotus [corrected] obliquus by induction of apoptosis in melanoma B16-F10 cells. J Ethnopharmacol 2009;121:221-8. https://doi.org/10.1016/j.jep.2008.10.016
- Chung MJ, Chung CK, Jeong Y, Ham SS. Anticancer activity of subfractions containing pure compounds of Chaga mushroom (Inonotus obliquus) extract in human cancer cells and in Balbc/c mice bearing Sarcoma-180 cells. Nutr Res Pract 2010;4:177-82. https://doi.org/10.4162/nrp.2010.4.3.177
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