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Erschienen in: Inflammation 5/2015

01.10.2015

Alpha-Tomatine Exhibits Anti-inflammatory Activity in Lipopolysaccharide-Activated Macrophages

verfasst von: Ben Zhao, Bing Zhou, Lei Bao, Yuming Yang, Kaijin Guo

Erschienen in: Inflammation | Ausgabe 5/2015

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Abstract

Alpha (α)-tomatine is the major saponin and occurs naturally in tomatoes, which has been confirmed to possess a variety of biological properties including antitumoral, antioxidant, and anti-inflammatory. However, the anti-inflammatory mechanism of α-tomatine is not well understood. This study aims to investigate the anti-inflammatory effects and mechanisms of α-tomatine. Results showed that α-tomatine significantly suppressed the production of pro-inflammatory cytokines in lipopolysaccharide (LPS)-induced macrophages. Moreover, LPS-mediated nuclear translocation of the nuclear factor-kappaB (NF-κB)-p65 and phosphorylation of extracellular signal-regulated kinase (ERK) 1/2 were attenuated after α-tomatine treatment. Still, LPS slightly promoted phosphorylation of Akt, and α-tomatine accelerated the phosphorylation of Akt in macrophages. Our findings indicate that α-tomatine may be a valuable therapeutic agent in the treatment of inflammation-related diseases.
Literatur
3.
Zurück zum Zitat Endo, Y., K. Blinova, et al. 2014. Differences in PGE2 production between primary human monocytes and differentiated macrophages: Role of IL-1beta and TRIF/IRF3. PLoS ONE 9(5): e98517.PubMedCentralCrossRefPubMed Endo, Y., K. Blinova, et al. 2014. Differences in PGE2 production between primary human monocytes and differentiated macrophages: Role of IL-1beta and TRIF/IRF3. PLoS ONE 9(5): e98517.PubMedCentralCrossRefPubMed
4.
5.
Zurück zum Zitat Becker, S., S. Mundandhara, et al. 2005. Regulation of cytokine production in human alveolar macrophages and airway epithelial cells in response to ambient air pollution particles: Further mechanistic studies. Toxicology and Applied Pharmacology 207(2 Suppl): 269–275.CrossRefPubMed Becker, S., S. Mundandhara, et al. 2005. Regulation of cytokine production in human alveolar macrophages and airway epithelial cells in response to ambient air pollution particles: Further mechanistic studies. Toxicology and Applied Pharmacology 207(2 Suppl): 269–275.CrossRefPubMed
6.
Zurück zum Zitat Kim, J.B., A.R. Han, et al. 2007. Inhibition of LPS-induced iNOS, COX-2 and cytokines expression by poncirin through the NF-kappaB inactivation in RAW 264.7 macrophage cells. Biological and Pharmaceutical Bulletin 30(12): 2345–2351.CrossRefPubMed Kim, J.B., A.R. Han, et al. 2007. Inhibition of LPS-induced iNOS, COX-2 and cytokines expression by poncirin through the NF-kappaB inactivation in RAW 264.7 macrophage cells. Biological and Pharmaceutical Bulletin 30(12): 2345–2351.CrossRefPubMed
7.
Zurück zum Zitat Herrera-Velit, P., K.L. Knutson, et al. 1997. Phosphatidylinositol 3-kinase-dependent activation of protein kinase C-zeta in bacterial lipopolysaccharide-treated human monocytes. Journal of Biological Chemistry 272(26): 16445–16452.CrossRefPubMed Herrera-Velit, P., K.L. Knutson, et al. 1997. Phosphatidylinositol 3-kinase-dependent activation of protein kinase C-zeta in bacterial lipopolysaccharide-treated human monocytes. Journal of Biological Chemistry 272(26): 16445–16452.CrossRefPubMed
8.
Zurück zum Zitat Moller, W., I. Heimbeck, et al. 2012. Differential inflammatory response to inhaled lipopolysaccharide targeted either to the airways or the alveoli in man. PLoS ONE 7(4): e33505.PubMedCentralCrossRefPubMed Moller, W., I. Heimbeck, et al. 2012. Differential inflammatory response to inhaled lipopolysaccharide targeted either to the airways or the alveoli in man. PLoS ONE 7(4): e33505.PubMedCentralCrossRefPubMed
10.
Zurück zum Zitat Moshkin, M.P., A.E. Akulov, et al. 2014. Proton magnetic resonance spectroscopy of brain metabolic shifts induced by acute administration of 2-deoxy-d-glucose and lipopolysaccharides. NMR in Biomedicine 27(4): 399–405.CrossRefPubMed Moshkin, M.P., A.E. Akulov, et al. 2014. Proton magnetic resonance spectroscopy of brain metabolic shifts induced by acute administration of 2-deoxy-d-glucose and lipopolysaccharides. NMR in Biomedicine 27(4): 399–405.CrossRefPubMed
11.
Zurück zum Zitat Aderem, A., and R.J. Ulevitch. 2000. Toll-like receptors in the induction of the innate immune response. Nature 406(6797): 782–787.CrossRefPubMed Aderem, A., and R.J. Ulevitch. 2000. Toll-like receptors in the induction of the innate immune response. Nature 406(6797): 782–787.CrossRefPubMed
12.
Zurück zum Zitat Guha, M., and N. Mackman. 2001. LPS induction of gene expression in human monocytes. Cellular Signalling 13(2): 85–94.CrossRefPubMed Guha, M., and N. Mackman. 2001. LPS induction of gene expression in human monocytes. Cellular Signalling 13(2): 85–94.CrossRefPubMed
13.
Zurück zum Zitat Kang, Y.J., U.R. Mbonye, et al. 2007. Regulation of intracellular cyclooxygenase levels by gene transcription and protein degradation. Progress in Lipid Research 46(2): 108–125.PubMedCentralCrossRefPubMed Kang, Y.J., U.R. Mbonye, et al. 2007. Regulation of intracellular cyclooxygenase levels by gene transcription and protein degradation. Progress in Lipid Research 46(2): 108–125.PubMedCentralCrossRefPubMed
14.
Zurück zum Zitat Caivano, M. 1998. Role of MAP kinase cascades in inducing arginine transporters and nitric oxide synthetase in RAW264 macrophages. FEBS Letters 429(3): 249–253.CrossRefPubMed Caivano, M. 1998. Role of MAP kinase cascades in inducing arginine transporters and nitric oxide synthetase in RAW264 macrophages. FEBS Letters 429(3): 249–253.CrossRefPubMed
15.
Zurück zum Zitat Akisue, T., T.W. Bauer, et al. 2002. The effect of particle wear debris on NFkappaB activation and pro-inflammatory cytokine release in differentiated THP-1 cells. Journal of Biomedial Materials Research 59(3): 507–515.CrossRef Akisue, T., T.W. Bauer, et al. 2002. The effect of particle wear debris on NFkappaB activation and pro-inflammatory cytokine release in differentiated THP-1 cells. Journal of Biomedial Materials Research 59(3): 507–515.CrossRef
16.
Zurück zum Zitat Lee, S.T., P.F. Wong, et al. 2013. Alpha-tomatine attenuation of in vivo growth of subcutaneous and orthotopic xenograft tumors of human prostate carcinoma PC-3 cells is accompanied by inactivation of nuclear factor-kappa B signaling. PLoS ONE 8(2): e57708.PubMedCentralCrossRefPubMed Lee, S.T., P.F. Wong, et al. 2013. Alpha-tomatine attenuation of in vivo growth of subcutaneous and orthotopic xenograft tumors of human prostate carcinoma PC-3 cells is accompanied by inactivation of nuclear factor-kappa B signaling. PLoS ONE 8(2): e57708.PubMedCentralCrossRefPubMed
17.
Zurück zum Zitat Friedman, M. 2002. Tomato glycoalkaloids: Role in the plant and in the diet. Journal of Agricultural and Food Chemistry 50(21): 5751–5780.CrossRefPubMed Friedman, M. 2002. Tomato glycoalkaloids: Role in the plant and in the diet. Journal of Agricultural and Food Chemistry 50(21): 5751–5780.CrossRefPubMed
18.
Zurück zum Zitat Friedman, M., C.E. Levin, et al. 2009. Tomatine-containing green tomato extracts inhibit growth of human breast, colon, liver, and stomach cancer cells. Journal of Agricultural and Food Chemistry 57(13): 5727–5733.CrossRefPubMed Friedman, M., C.E. Levin, et al. 2009. Tomatine-containing green tomato extracts inhibit growth of human breast, colon, liver, and stomach cancer cells. Journal of Agricultural and Food Chemistry 57(13): 5727–5733.CrossRefPubMed
19.
Zurück zum Zitat Friedman, M. 2013. Anticarcinogenic, cardioprotective, and other health benefits of tomato compounds lycopene, alpha-tomatine, and tomatidine in pure form and in fresh and processed tomatoes. Journal of Agricultural and Food Chemistry 61(40): 9534–9550.CrossRefPubMed Friedman, M. 2013. Anticarcinogenic, cardioprotective, and other health benefits of tomato compounds lycopene, alpha-tomatine, and tomatidine in pure form and in fresh and processed tomatoes. Journal of Agricultural and Food Chemistry 61(40): 9534–9550.CrossRefPubMed
20.
Zurück zum Zitat Pierce, G.F. 1990. Macrophages: important physiologic and pathologic sources of polypeptide growth factors. American Journal of Respiratory Cell and Molecular Biology 2(3): 233–234.CrossRefPubMed Pierce, G.F. 1990. Macrophages: important physiologic and pathologic sources of polypeptide growth factors. American Journal of Respiratory Cell and Molecular Biology 2(3): 233–234.CrossRefPubMed
21.
Zurück zum Zitat Wadleigh, D.J., S.T. Reddy, et al. 2000. Transcriptional activation of the cyclooxygenase-2 gene in endotoxin-treated RAW 264.7 macrophages. Journal of Biological Chemistry 275(9): 6259–6266.CrossRefPubMed Wadleigh, D.J., S.T. Reddy, et al. 2000. Transcriptional activation of the cyclooxygenase-2 gene in endotoxin-treated RAW 264.7 macrophages. Journal of Biological Chemistry 275(9): 6259–6266.CrossRefPubMed
22.
Zurück zum Zitat Muller, J.M., H.W. Ziegler-Heitbrock, et al. 1993. Nuclear factor kappa B, a mediator of lipopolysaccharide effects. Immunobiology 187(3–5): 233–256.CrossRefPubMed Muller, J.M., H.W. Ziegler-Heitbrock, et al. 1993. Nuclear factor kappa B, a mediator of lipopolysaccharide effects. Immunobiology 187(3–5): 233–256.CrossRefPubMed
23.
Zurück zum Zitat Vane, J.R., J.A. Mitchell, et al. 1994. Inducible isoforms of cyclooxygenase and nitric-oxide synthase in inflammation. Proceedings of the National Academy of Sciences of the United States of America 91(6): 2046–2050.PubMedCentralCrossRefPubMed Vane, J.R., J.A. Mitchell, et al. 1994. Inducible isoforms of cyclooxygenase and nitric-oxide synthase in inflammation. Proceedings of the National Academy of Sciences of the United States of America 91(6): 2046–2050.PubMedCentralCrossRefPubMed
24.
Zurück zum Zitat Osborn, L., S. Kunkel, et al. 1989. Tumor necrosis factor alpha and interleukin 1 stimulate the human immunodeficiency virus enhancer by activation of the nuclear factor kappa B. Proceedings of the National Academy of Sciences of the United States of America 86(7): 2336–2340.PubMedCentralCrossRefPubMed Osborn, L., S. Kunkel, et al. 1989. Tumor necrosis factor alpha and interleukin 1 stimulate the human immunodeficiency virus enhancer by activation of the nuclear factor kappa B. Proceedings of the National Academy of Sciences of the United States of America 86(7): 2336–2340.PubMedCentralCrossRefPubMed
25.
Zurück zum Zitat Ducharme, E., and J.M. Weinberg. 2008. Etanercept. Expert Opinion on Biological Therapy 8(4): 491–502.CrossRefPubMed Ducharme, E., and J.M. Weinberg. 2008. Etanercept. Expert Opinion on Biological Therapy 8(4): 491–502.CrossRefPubMed
26.
Zurück zum Zitat Beutler, B., and A. Cerami. 1989. The biology of cachectin/TNF—a primary mediator of the host response. Annual Review of Immunology 7: 625–655.CrossRefPubMed Beutler, B., and A. Cerami. 1989. The biology of cachectin/TNF—a primary mediator of the host response. Annual Review of Immunology 7: 625–655.CrossRefPubMed
27.
28.
Zurück zum Zitat Baeuerle, P.A., and T. Henkel. 1994. Function and activation of NF-kappa B in the immune system. Annual Review of Immunology 12: 141–179.CrossRefPubMed Baeuerle, P.A., and T. Henkel. 1994. Function and activation of NF-kappa B in the immune system. Annual Review of Immunology 12: 141–179.CrossRefPubMed
29.
Zurück zum Zitat Vallabhapurapu, S., and M. Karin. 2009. Regulation and function of NF-kappaB transcription factors in the immune system. Annual Review of Immunology 27: 693–733.CrossRefPubMed Vallabhapurapu, S., and M. Karin. 2009. Regulation and function of NF-kappaB transcription factors in the immune system. Annual Review of Immunology 27: 693–733.CrossRefPubMed
30.
Zurück zum Zitat Baeuerle, P.A. 1998. IkappaB-NF-kappaB structures: At the interface of inflammation control. Cell 95(6): 729–731.CrossRefPubMed Baeuerle, P.A. 1998. IkappaB-NF-kappaB structures: At the interface of inflammation control. Cell 95(6): 729–731.CrossRefPubMed
31.
Zurück zum Zitat DiDonato, J., F. Mercurio, et al. 1996. Mapping of the inducible IkappaB phosphorylation sites that signal its ubiquitination and degradation. Molecular and Cellular Biology 16(4): 1295–1304.PubMedCentralPubMed DiDonato, J., F. Mercurio, et al. 1996. Mapping of the inducible IkappaB phosphorylation sites that signal its ubiquitination and degradation. Molecular and Cellular Biology 16(4): 1295–1304.PubMedCentralPubMed
32.
Zurück zum Zitat Sanchez-Perez, I., S.A. Benitah, et al. 2002. Cell stress and MEKK1-mediated c-Jun activation modulate NFkappaB activity and cell viability. Molecular Biology of the Cell 13(8): 2933–2945.PubMedCentralCrossRefPubMed Sanchez-Perez, I., S.A. Benitah, et al. 2002. Cell stress and MEKK1-mediated c-Jun activation modulate NFkappaB activity and cell viability. Molecular Biology of the Cell 13(8): 2933–2945.PubMedCentralCrossRefPubMed
33.
Zurück zum Zitat de Martin, R., B. Vanhove, et al. 1993. Cytokine-inducible expression in endothelial cells of an I kappa B alpha-like gene is regulated by NF kappa B. EMBO Journal 12(7): 2773–2779.PubMedCentralPubMed de Martin, R., B. Vanhove, et al. 1993. Cytokine-inducible expression in endothelial cells of an I kappa B alpha-like gene is regulated by NF kappa B. EMBO Journal 12(7): 2773–2779.PubMedCentralPubMed
34.
Zurück zum Zitat Surh, Y.J., K.S. Chun, et al. 2001. Molecular mechanisms underlying chemopreventive activities of anti-inflammatory phytochemicals: down-regulation of COX-2 and iNOS through suppression of NF-kappa B activation. Mutation Research 480–481: 243–268.CrossRefPubMed Surh, Y.J., K.S. Chun, et al. 2001. Molecular mechanisms underlying chemopreventive activities of anti-inflammatory phytochemicals: down-regulation of COX-2 and iNOS through suppression of NF-kappa B activation. Mutation Research 480–481: 243–268.CrossRefPubMed
35.
Zurück zum Zitat Lappas, M., M. Permezel, et al. 2002. Nuclear factor kappa B regulation of proinflammatory cytokines in human gestational tissues in vitro. Biology of Reproduction 67(2): 668–673.CrossRefPubMed Lappas, M., M. Permezel, et al. 2002. Nuclear factor kappa B regulation of proinflammatory cytokines in human gestational tissues in vitro. Biology of Reproduction 67(2): 668–673.CrossRefPubMed
36.
Zurück zum Zitat Brown, K., S. Gerstberger, et al. 1995. Control of I kappa B-alpha proteolysis by site-specific, signal-induced phosphorylation. Science 267(5203): 1485–1488.CrossRefPubMed Brown, K., S. Gerstberger, et al. 1995. Control of I kappa B-alpha proteolysis by site-specific, signal-induced phosphorylation. Science 267(5203): 1485–1488.CrossRefPubMed
37.
Zurück zum Zitat O’Connell, M.A., B.L. Bennett, et al. 1998. Role of IKK1 and IKK2 in lipopolysaccharide signaling in human monocytic cells. Journal of Biological Chemistry 273(46): 30410–30414.CrossRefPubMed O’Connell, M.A., B.L. Bennett, et al. 1998. Role of IKK1 and IKK2 in lipopolysaccharide signaling in human monocytic cells. Journal of Biological Chemistry 273(46): 30410–30414.CrossRefPubMed
38.
Zurück zum Zitat Won, J.H., H.T. Im, et al. 2006. Anti-inflammatory effect of buddlejasaponin IV through the inhibition of iNOS and COX-2 expression in RAW 264.7 macrophages via the NF-kappaB inactivation. British Journal of Pharmacology 148(2): 216–225.PubMedCentralCrossRefPubMed Won, J.H., H.T. Im, et al. 2006. Anti-inflammatory effect of buddlejasaponin IV through the inhibition of iNOS and COX-2 expression in RAW 264.7 macrophages via the NF-kappaB inactivation. British Journal of Pharmacology 148(2): 216–225.PubMedCentralCrossRefPubMed
39.
Zurück zum Zitat Robinson, M.J., and M.H. Cobb. 1997. Mitogen-activated protein kinase pathways. Current Opinion in Cell Biology 9(2): 180–186.CrossRefPubMed Robinson, M.J., and M.H. Cobb. 1997. Mitogen-activated protein kinase pathways. Current Opinion in Cell Biology 9(2): 180–186.CrossRefPubMed
40.
Zurück zum Zitat Caivano, M. 1998. Role of MAP kinase cascades in inducing arginine transporters and nitric oxide synthetase in RAW264 macrophages. FEBS Letters 429(3): 249–253.CrossRefPubMed Caivano, M. 1998. Role of MAP kinase cascades in inducing arginine transporters and nitric oxide synthetase in RAW264 macrophages. FEBS Letters 429(3): 249–253.CrossRefPubMed
41.
Zurück zum Zitat Vanden Berghe, W., S. Plaisance, et al. 1998. p38 and extracellular signal-regulated kinase mitogen-activated protein kinase pathways are required for nuclear factor-kappaB p65 transactivation mediated by tumor necrosis factor. Journal of Biological Chemistry 273(6): 3285–3290.CrossRefPubMed Vanden Berghe, W., S. Plaisance, et al. 1998. p38 and extracellular signal-regulated kinase mitogen-activated protein kinase pathways are required for nuclear factor-kappaB p65 transactivation mediated by tumor necrosis factor. Journal of Biological Chemistry 273(6): 3285–3290.CrossRefPubMed
42.
Zurück zum Zitat Dai, J.N., Y. Zong, et al. 2011. Gastrodin inhibits expression of inducible NO synthase, cyclooxygenase-2 and proinflammatory cytokines in cultured LPS-stimulated microglia via MAPK pathways. PLoS ONE 6(7): e21891.PubMedCentralCrossRefPubMed Dai, J.N., Y. Zong, et al. 2011. Gastrodin inhibits expression of inducible NO synthase, cyclooxygenase-2 and proinflammatory cytokines in cultured LPS-stimulated microglia via MAPK pathways. PLoS ONE 6(7): e21891.PubMedCentralCrossRefPubMed
43.
Zurück zum Zitat Liu, H.T., P. Huang, et al. 2011. Chitosan oligosaccharides suppress LPS-induced IL-8 expression in human umbilical vein endothelial cells through blockade of p38 and Akt protein kinases. Acta Pharmacologica Sinica 32(4): 478–486.PubMedCentralCrossRefPubMed Liu, H.T., P. Huang, et al. 2011. Chitosan oligosaccharides suppress LPS-induced IL-8 expression in human umbilical vein endothelial cells through blockade of p38 and Akt protein kinases. Acta Pharmacologica Sinica 32(4): 478–486.PubMedCentralCrossRefPubMed
44.
Zurück zum Zitat Guha, M., and N. Mackman. 2002. The phosphatidylinositol 3-kinase-Akt pathway limits lipopolysaccharide activation of signaling pathways and expression of inflammatory mediators in human monocytic cells. Journal of Biological Chemistry 277(35): 32124–32132.CrossRefPubMed Guha, M., and N. Mackman. 2002. The phosphatidylinositol 3-kinase-Akt pathway limits lipopolysaccharide activation of signaling pathways and expression of inflammatory mediators in human monocytic cells. Journal of Biological Chemistry 277(35): 32124–32132.CrossRefPubMed
45.
Zurück zum Zitat Aksoy, E., W. Vanden Berghe, et al. 2005. Inhibition of phosphoinositide 3-kinase enhances TRIF-dependent NF-kappa B activation and IFN-beta synthesis downstream of Toll-like receptor 3 and 4. European Journal of Immunology 35(7): 2200–2209.CrossRefPubMed Aksoy, E., W. Vanden Berghe, et al. 2005. Inhibition of phosphoinositide 3-kinase enhances TRIF-dependent NF-kappa B activation and IFN-beta synthesis downstream of Toll-like receptor 3 and 4. European Journal of Immunology 35(7): 2200–2209.CrossRefPubMed
46.
Zurück zum Zitat Luyendyk, J.P., G.A. Schabbauer, et al. 2008. Genetic analysis of the role of the PI3K-Akt pathway in lipopolysaccharide-induced cytokine and tissue factor gene expression in monocytes/macrophages. Journal of Immunology 180(6): 4218–4226.CrossRef Luyendyk, J.P., G.A. Schabbauer, et al. 2008. Genetic analysis of the role of the PI3K-Akt pathway in lipopolysaccharide-induced cytokine and tissue factor gene expression in monocytes/macrophages. Journal of Immunology 180(6): 4218–4226.CrossRef
47.
Zurück zum Zitat Ha, Y.M., S.A. Ham, et al. 2011. beta(1)-adrenergic receptor-mediated HO-1 induction, via PI3K and p38 MAPK, by isoproterenol in RAW 264.7 cells leads to inhibition of HMGB1 release in LPS-activated RAW 264.7 cells and increases in survival rate of CLP-induced septic mice. Biochemical Pharmacology 82(7): 769–777.CrossRefPubMed Ha, Y.M., S.A. Ham, et al. 2011. beta(1)-adrenergic receptor-mediated HO-1 induction, via PI3K and p38 MAPK, by isoproterenol in RAW 264.7 cells leads to inhibition of HMGB1 release in LPS-activated RAW 264.7 cells and increases in survival rate of CLP-induced septic mice. Biochemical Pharmacology 82(7): 769–777.CrossRefPubMed
48.
Zurück zum Zitat Madrid, L.V., C.Y. Wang, et al. 2000. Akt suppresses apoptosis by stimulating the transactivation potential of the RelA/p65 subunit of NF-kappaB. Molecular and Cellular Biology 20(5): 1626–1638.PubMedCentralCrossRefPubMed Madrid, L.V., C.Y. Wang, et al. 2000. Akt suppresses apoptosis by stimulating the transactivation potential of the RelA/p65 subunit of NF-kappaB. Molecular and Cellular Biology 20(5): 1626–1638.PubMedCentralCrossRefPubMed
49.
Zurück zum Zitat Madrid, L.V., M.W. Mayo, et al. 2001. Akt stimulates the transactivation potential of the RelA/p65 Subunit of NF-kappa B through utilization of the Ikappa B kinase and activation of the mitogen-activated protein kinase p38. Journal of Biological Chemistry 276(22): 18934–18940.CrossRefPubMed Madrid, L.V., M.W. Mayo, et al. 2001. Akt stimulates the transactivation potential of the RelA/p65 Subunit of NF-kappa B through utilization of the Ikappa B kinase and activation of the mitogen-activated protein kinase p38. Journal of Biological Chemistry 276(22): 18934–18940.CrossRefPubMed
50.
Zurück zum Zitat Shieh, J.M., T.H. Cheng, et al. 2011. Alpha-Tomatine suppresses invasion and migration of human non-small cell lung cancer NCI-H460 cells through inactivating FAK/PI3K/Akt signaling pathway and reducing binding activity of NF-kappaB. Cell Biochemistry and Biophysics 60(3): 297–310.CrossRefPubMed Shieh, J.M., T.H. Cheng, et al. 2011. Alpha-Tomatine suppresses invasion and migration of human non-small cell lung cancer NCI-H460 cells through inactivating FAK/PI3K/Akt signaling pathway and reducing binding activity of NF-kappaB. Cell Biochemistry and Biophysics 60(3): 297–310.CrossRefPubMed
51.
Zurück zum Zitat Shih, Y.W., J.M. Shieh, et al. 2009. Alpha-tomatine inactivates PI3K/Akt and ERK signaling pathways in human lung adenocarcinoma A549 cells: Effect on metastasis. Food and Chemical Toxicology 47(8): 1985–1995.CrossRefPubMed Shih, Y.W., J.M. Shieh, et al. 2009. Alpha-tomatine inactivates PI3K/Akt and ERK signaling pathways in human lung adenocarcinoma A549 cells: Effect on metastasis. Food and Chemical Toxicology 47(8): 1985–1995.CrossRefPubMed
Metadaten
Titel
Alpha-Tomatine Exhibits Anti-inflammatory Activity in Lipopolysaccharide-Activated Macrophages
verfasst von
Ben Zhao
Bing Zhou
Lei Bao
Yuming Yang
Kaijin Guo
Publikationsdatum
01.10.2015
Verlag
Springer US
Erschienen in
Inflammation / Ausgabe 5/2015
Print ISSN: 0360-3997
Elektronische ISSN: 1573-2576
DOI
https://doi.org/10.1007/s10753-015-0154-9

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