참고문헌
- Aggarwal, B.B., Shishodia, S., Sandur, S.K., Pandey, M.K. and Sethi, G. (2006) Inflammation and cancer: how hot is the link? Biochem. Pharmacol. 72, 1605-1621 https://doi.org/10.1016/j.bcp.2006.06.029
- Martey, C.A., Pollock, S.J., Turner, C.K., O'Reilly, K.M., Baglole, C.J., Phipps, R.P. and Sime, P.J. (2004) Cigarette smoke induces cyclooxygenase-2 and microsomal prostaglandin E2 synthase in human lung fibroblasts: implications for lung inflammation and cancer. Am. J. Physiol. Lung Cell Mol. Physiol. 287, L981-991 https://doi.org/10.1152/ajplung.00239.2003
- Peek, R.M., Jr. and Crabtree, J.E. (2006) Helicobacter infection and gastric neoplasia. J. Pathol. 208, 233-248 https://doi.org/10.1002/path.1868
- Geller, D.A., Nussler, A.K., Di Silvio, M., Lowenstein, C.J., Shapiro, R.A., Wang, S.C., Simmons, R.L. and Billiar, T.R. (1993) Cytokines, endotoxin, and glucocorticoids regulate the expression of inducible nitric oxide synthase in hepatocytes. Proc. Natl. Acad. Sci. U.S.A. 90, 522-526. https://doi.org/10.1073/pnas.90.2.522
- Navikas, V., Haglund, M., Link, J., He, B., Lindqvist, L., Fredrikson, S. and Link, H. (1995) Cytokine mRNA profiles in mononuclear cells in acute aseptic meningoencephalitis. Infect. Immun. 63, 1581-1586
- Ulich, T.R., Guo, K., Yin, S., del Castillo, J., Yi, E.S., Thompson, R.C. and Eisenberg, S.P. (1992) Endotoxin-induced cytokine gene expression in vivo. IV. Expression of interleukin-1 alpha/beta and interleukin-1 receptor antagonist mRNA during endotoxemia and during endotoxin-initiated local acute inflammation. Am. J. Pathol. 141, 61-68
- Campa, V.M., Iglesias, J.M., Carcedo, M.T., Rodriguez, R., Riera, J., Ramos, S. and Lazo, P.S. (2005) Polyinosinic acid induces TNF and NO production as well as NF-kappaB and AP-1 transcriptional activation in the monocytemacrophage cell line RAW 264.7. Inflamm. Res. 54, 328-337 https://doi.org/10.1007/s00011-005-1359-4
- Shin, Y.H., Son, K.N., Lee, G.W., Kwon, B.S. and Kim, J. (2005) Transcriptional regulation of human CC chemokine CCL15 gene by NF-kappaB and AP-1 elements in PMA-stimulated U937 monocytoid cells. Biochim. Biophys. Acta. 1732, 38-42 https://doi.org/10.1016/j.bbaexp.2005.11.001
- Hsu, T.C., Young, M.R., Cmarik, J. and Colburn, N.H. (2000) Activator protein 1 (AP-1)- and nuclear factor kappaB (NF-kappaB)-dependent transcriptional events in carcinogenesis. Free Radic. Biol. Med. 28, 1338-1348 https://doi.org/10.1016/S0891-5849(00)00220-3
- Karin, M. and Lin, A. (2002) NF-kappaB at the crossroads of life and death. Nat. Immunol. 3, 221-227 https://doi.org/10.1038/ni0302-221
- Uzzo, R.G., Crispen, P.L., Golovine, K., Makhov, P., Horwitz, E.M. and Kolenko, V.M. (2006) Diverse effects of zinc on NF-kappaB and AP-1 transcription factors: implications for prostate cancer progression. Carcinogenesis 27, 1980-1990 https://doi.org/10.1093/carcin/bgl034
- Dong, Z., Birrer, M.J., Watts, R.G., Matrisian, L.M. and Colburn, N.H. (1994) Blocking of tumor promoter-induced AP-1 activity inhibits induced transformation in JB6 mouse epidermal cells. Proc. Natl. Acad. Sci. U.S.A. 91, 609-613 https://doi.org/10.1073/pnas.91.2.609
- Li, J.J., Dong, Z., Dawson, M.I. and Colburn, N.H. (1996) Inhibition of tumor promoter-induced transformation by retinoids that transrepress AP-1 without transactivating retinoic acid response element. Cancer Res. 56, 483-489
- Budagian, V., Bulanova, E., Brovko, L., Orinska, Z., Fayad, R., Paus, R. and Bulfone-Paus, S. (2003) Signaling through P2X7 receptor in human T cells involves p56lck, MAP kinases, and transcription factors AP-1 and NF-kappa B. J. Biol. Chem. 278, 1549-1560 https://doi.org/10.1074/jbc.M206383200
- Ma, W., Gee, K., Lim, W., Chambers, K., Angel, J.B., Kozlowski, M. and Kumar, A. (2004) Dexamethasone inhibits IL-12p40 production in lipopolysaccharide-stimulated human monocytic cells by down-regulating the activity of c-Jun N-terminal kinase, the activation protein-1, and NF-kappa B transcription factors. J. Immunol. 172, 318-330 https://doi.org/10.4049/jimmunol.172.1.318
- Jin, R., Wan, L.L., Mitsuishi, T., Kodama, K. and Kurashige, S. (1994) Immunomodulative effects of Chinese herbs in mice treated with anti-tumor agent cyclophosphamide. Yakugaku. Zasshi. 114, 533-538 https://doi.org/10.1248/yakushi1947.114.7_533
- Chung, H.S., Kang, M., Cho, C., Park, S., Kim, H., Yoon, Y.S., Kang, J., Shin, M.K., Hong, M.C. and Bae, H. (2005) Inhibition of lipopolysaccharide and interferon-gamma-induced expression of inducible nitric oxide synthase and tumor necrosis factor-alpha by Lithospermi radix in mouse peritoneal macrophages. J. Ethnopharmacol. 102, 412-417 https://doi.org/10.1016/j.jep.2005.06.028
- Jin, R. and Kurashige, S. (1996) Effects of Chinese herbs on macrophage functions in N-butyl-N-butanolnitrosoamine treated mice. Immunopharmacol. Immunotoxicol. 18, 105-114 https://doi.org/10.3109/08923979609007113
- Chen, X., Yang, L., Zhang, N., Turpin, J.A., Buckheit, R.W., Osterling, C., Oppenheim, J.J. and Howard, O.M. (2003) Shikonin, a component of chinese herbal medicine, inhibits chemokine receptor function and suppresses human immunodeficiency virus type 1. Antimicrob. Agents Chemother. 47, 2810-2816 https://doi.org/10.1128/AAC.47.9.2810-2816.2003
- Lirussi, D., Li, J., Prieto, J.M., Gennari, M., Buschiazzo, H., Rios, J.L. and Zaidenberg, A. (2004) Inhibition of Trypanosoma cruzi by plant extracts used in Chinese medicine. Fitoterapia. 75, 718-723 https://doi.org/10.1016/j.fitote.2004.09.017
- Anest, V., Hanson, J.L., Cogswell, P.C., Steinbrecher, K.A., Strahl, B.D. and Baldwin, A.S. (2003) A nucleosomal function for IkappaB kinase-alpha in NF-kappaB-dependent gene expression. Nature 423, 659-663 https://doi.org/10.1038/nature01648
- Krens, S.F., Spaink, H.P. and Snaar-Jagalska, B.E. (2006) Functions of the MAPK family in vertebrate-development. FEBS Lett. 580, 4984-4990 https://doi.org/10.1016/j.febslet.2006.08.025
- Cano, E. and Mahadevan, L.C. (1995) Parallel signal processing among mammalian MAPKs. Trends Biochem. Sci. 20, 117-122 https://doi.org/10.1016/S0968-0004(00)88978-1
- Carter, A.B., Knudtson, K.L., Monick, M.M. and Hunninghake, G.W. (1999) The p38 mitogen-activated protein kinase is required for NF-kappaB-dependent gene expression. The role of TATA-binding protein (TBP). J. Biol. Chem. 274, 30858-30863 https://doi.org/10.1074/jbc.274.43.30858
- Mechta-Grigoriou, F., Gerald, D. and Yaniv, M. (2001) The mammalian Jun proteins: redundancy and specificity. Oncogene 20, 2378-2389 https://doi.org/10.1038/sj.onc.1204381
- Chang, Y.H., Hsieh, S.L., Chen, M.C. and Lin, W.W. (2002) Lymphotoxin beta receptor induces interleukin 8 gene expression via NF-kappaB and AP-1 activation. Exp. Cell Res. 278, 166-174 https://doi.org/10.1006/excr.2002.5573
- Yao, J., Mackman, N., Edgington, T.S. and Fan, S.T. (1997) Lipopolysaccharide induction of the tumor necrosis factor-alpha promoter in human monocytic cells. Regulation by Egr-1, c-Jun, and NF-kappaB transcription factors. J. Biol. Chem. 272, 17795-17801 https://doi.org/10.1074/jbc.272.28.17795
- Minden, A., Lin, A., Smeal, T., Derijard, B., Cobb, M., Davis, R. and Karin, M. (1994) c-Jun N-terminal phosphorylation correlates with activation of the JNK subgroup but not the ERK subgroup of mitogen-activated protein kinases. Mol. Cell. Biol. 14, 6683-6688 https://doi.org/10.1128/MCB.14.10.6683
- Somboonwiwat, K., Supungul, P., Rimphanitchayakit, V., Aoki, T., Hirono, I., Tassanakajon, A. (2006) Differentially expressed genes in hemocytes of Vibrio harveyi-challenged shrimp Penaeus monodon. J. Biochem. Mol. Biol. 39, 26-36 https://doi.org/10.5483/BMBRep.2006.39.1.026
피인용 문헌
- Flavonoids inhibit the AU-rich element binding of HuC vol.42, pp.1, 2009, https://doi.org/10.5483/BMBRep.2009.42.1.041
- The topical application of low-temperature argon plasma enhances the anti-inflammatory effect of Jaun-ointment on DNCB-induced NC/Nga mice vol.17, pp.1, 2017, https://doi.org/10.1186/s12906-017-1850-9
- Gelam Honey Scavenges Peroxynitrite During the Immune Response vol.13, pp.12, 2012, https://doi.org/10.3390/ijms130912113
- Topical Herbal Formulae in the Management of Psoriasis: Systematic Review with Meta-Analysis of Clinical Studies and Investigation of the Pharmacological Actions of the Main Herbs vol.28, pp.4, 2014, https://doi.org/10.1002/ptr.5028
- The regulation of iron metabolism in the mononuclear phagocyte system vol.6, pp.4, 2013, https://doi.org/10.1586/17474086.2013.814840
- Oral acute and chronic toxicity studies of β, β-dimethylacrylalkannin in mice and rats vol.4, pp.2, 2017, https://doi.org/10.2131/fts.4.45
- The role of peroxidases in the pathogenesis of atherosclerosis vol.44, pp.8, 2011, https://doi.org/10.5483/BMBRep.2011.44.8.497
- Anti-inflammatory and barrier protecting effect of Lithospermum erythrorhizon extracts in chronic oxazolone-induced murine atopic dermatitis vol.56, pp.1, 2009, https://doi.org/10.1016/j.jdermsci.2009.07.001
- Curcuminoids Modulate the PKCδ/NADPH Oxidase/Reactive Oxygen Species Signaling Pathway and Suppress Matrix Invasion during Monocyte–Macrophage Differentiation vol.63, pp.40, 2015, https://doi.org/10.1021/acs.jafc.5b04083
- Oral Chinese herbal medicine combined with pharmacotherapy for psoriasis vulgaris: a systematic review vol.53, pp.11, 2014, https://doi.org/10.1111/ijd.12607
- Inhibition of inflammatory mediators and reactive oxygen and nitrogen species by some depsidones and diaryl ether derivatives isolated fromCorynespora cassiicola, an endophytic fungus ofGongronema latifoliumleaves vol.35, pp.6, 2013, https://doi.org/10.3109/08923973.2013.834930
- The anti-inflammatory effect of Lithospermum Erythrorhizon on lipopolysaccharide - induced inflammatory response in RAW 264.7 cells vol.28, pp.2, 2013, https://doi.org/10.6116/kjh.2013.28.2.67
- Acute and 28-Day Subacute Toxicity Studies of Hexane Extracts of the Roots of Lithospermum erythrorhizon in Sprague-Dawley Rats vol.31, pp.4, 2015, https://doi.org/10.5487/TR.2015.31.4.403
- Protective Effects of Lithospermum erythrorhizon Against Cerulein-Induced Acute Pancreatitis vol.44, pp.1, 2015, https://doi.org/10.1097/MPA.0000000000000195