References
- Ahsan, H., Reagan-Shaw, S., Breur, J. and Ahmad, N. 2007. Sanguinarine induces apoptosis of human pancreatic carcinoma AsPC-1 and BxPC-3 cells via modulationsin Bcl-2 family proteins. Cancer Lett. 249, 198-208. https://doi.org/10.1016/j.canlet.2006.08.018
- Basini, G., Bussolati, S., Santini, S. E. and Grasselli, F. 2007. Sanguinarine inhibits VEGF-induced angiogenesis in a fibrin gel matrix. Biofactors 29, 11-18. https://doi.org/10.1002/biof.5520290102
- Billen, L. P., Shamas-Din, A. and Andrews, D. W. 2008. Bid: a Bax-like BH3 protein. Oncogene 27, S93-104. https://doi.org/10.1038/onc.2009.47
- Cecen, E., Altun, Z., Ercetin, P., Aktas, S. and Olgun, N. 2014. Promoting effects of sanguinarine on apoptotic gene expression in human neuroblastoma cells. Asian Pac. J. Cancer Prev. 15, 9445-9451. https://doi.org/10.7314/APJCP.2014.15.21.9445
- Chang, M. C., Chan, C. P., Wang, Y. J., Lee, P. H., Chen, L. I., Tsai, Y. L., Lin, B. R., Wang, Y. L. and Jeng, J. H. 2007. Induction of necrosis and apoptosis to KB cancer cells by sanguinarine is associated with reactive oxygen species production and mitochondrial membrane depolarization. Toxicol. Appl. Pharmacol. 218,143-151. https://doi.org/10.1016/j.taap.2006.10.025
- Choi, W. Y., Kim, G. Y., Lee, W. H. and Choi, Y. H. 2008. Sanguinarine, a benzophenanthridine alkaloid, induces apoptosis in MDA-MB-231 human breast carcinoma cells through a reactive oxygen species-mediated mitochondrial pathway. Chemotherapy 54, 279-287. https://doi.org/10.1159/000149719
- Choi, Y. H., Choi, W. Y., Hong, S. H., Kim, S. O., Kim, G. Y., Lee, W. H. and Yoo, Y. H. 2009. Anti-invasive activity of sanguinarine through modulation of tight junctions and matrix metalloproteinase activities in MDA-MB-231 human breast carcinoma cells. Chem. Biol. Interact. 179, 185-191. https://doi.org/10.1016/j.cbi.2008.11.009
- Cragg, G. M. and Newman, D. J. 2005. Plants as a source of anti-cancer agents. J. Ethnopharmacol. 100, 72-79. https://doi.org/10.1016/j.jep.2005.05.011
- Decker, P. and Muller, S. 2002. Modulating poly (ADP-ribose) polymerase activity: potential for the prevention and therapy of pathogenic situations involving DNA damage and oxidative stress. Curr. Pharm. Biotechnol. 3, 275-283. https://doi.org/10.2174/1389201023378265
- Eun, J. P. and Koh, G. Y. 2004. Suppression of angiogenesis by the plant alkaloid, sanguinarine. Biochem. Biophys. Res. Commun. 317, 618-624. https://doi.org/10.1016/j.bbrc.2004.03.077
- Firatli, E., Unal, T., Onan, U. and Sandalli, P. 1994. Antioxidative activities of some chemotherapeutics. A possible mechanism in reducing gingival inflammation. J. Clin. Periodontol. 21, 680-683. https://doi.org/10.1111/j.1600-051X.1994.tb00786.x
- Frankos, V. H., Brusick, D. J., Johnson, E. M., Maibach, H. I., Munro, I., Squire, R. A. and Weil, C. S. 1990. Safety of Sanguinaria extract as used in commercial toothpaste and oral rinse products. J. Can. Dent. Assoc. 56, S41-47.
- Fridlender, M., Kapulnik, Y. and Koltai, H. 2015. Plant derived substances with anti-cancer activity: from folklore to practice. Front. Plant Sci. 6, 799.
- Fulda, S. and Debatin, K. M. 2006. Extrinsic versus intrinsic apoptosis pathways in anticancer chemotherapy. Oncogene 25, 4798-4811. https://doi.org/10.1038/sj.onc.1209608
- Gaziano, R., Moroni, G., Bue, C., Miele, M. T., Sinibaldi-Vallebona, P. and Pica, F. 2016. Antitumor effects of the benzophenanthridine alkaloid sanguinarine: Evidence and perspectives. World J. Gastrointest. Oncol. 8, 30-39. https://doi.org/10.4251/wjgo.v8.i1.30
- Gupta, S. C., Kim, J. H., Prasad, S. and Aggarwal, B. B. 2010. Regulation of survival, proliferation, invasion, angiogenesis, and metastasis of tumor cells through modulation of inflammatory pathways by nutraceuticals. Cancer Metastasis Rev. 29, 405-434. https://doi.org/10.1007/s10555-010-9235-2
- Hajra, K. M. and Liu, J. R. 2004. Apoptosome dysfunction in human cancer. Apoptosis 9, 691-704. https://doi.org/10.1023/B:APPT.0000045786.98031.1d
- Han, M. H., Kim, G. Y., Yoo, Y. H. and Choi, Y. H. 2013. Sanguinarine induces apoptosis in human colorectal cancer HCT-116 cells through ROS-mediated Egr-1 activation and mitochondrial dysfunction. Toxicol. Lett. 220, 157-166. https://doi.org/10.1016/j.toxlet.2013.04.020
- Han, M. H., Kim, S. O., Kim, G. Y., Kwon, T. K., Choi, B. T., Lee, W. H. and Choi, Y. H. 2007. Induction of apoptosis by sanguinarine in C6 rat glioblastoma cells is associated with the modulation of the Bcl-2 family and activation of caspases through downregulation of extracellular signal-regulated kinase and Akt. Anticancer Drugs 18, 913-921.
- Han, M. H., Park, C., Jin, C. Y., Kim, G. Y., Chang, Y. C., Moon, S. K., Kim, W. J. and Choi, Y. H. 2013. Apoptosis induction of human bladder cancer cells by sanguinarine through reactive oxygen species-mediated up-regulation of early growth response gene-1. PLoS One 8, e63425. https://doi.org/10.1371/journal.pone.0063425
- Han, M. H., Yoo, Y. H. and Choi, Y. H. 2008. Sanguinarineinduced apoptosis in human leukemia U937 cells via Bcl-2 downregulation and caspase-3 activation. Chemotherapy 54, 157-165. https://doi.org/10.1159/000140359
- Hata, A. N., Engelman, J. A. and Faber, A. C. 2015. The BCL2 family: Key mediators of the apoptotic response to targeted anticancer therapeutics. Cancer Discov. 5, 475-487. https://doi.org/10.1158/2159-8290.CD-15-0011
- Hong, S. J., Jeong, S. S. and Song, K. B. 2005. Effects of sanguinaria in fluoride-containing dentifrices on the remineralisation of subsurface carious lesion in vitro. Int. Dent. J. 55, 128-132. https://doi.org/10.1111/j.1875-595X.2005.tb00309.x
- Kantari, C. and Walczak, H. 2011. Caspase-8 and bid: caught in the act between death receptors and mitochondria. Biochim. Biophys. Acta. 1813, 558-563. https://doi.org/10.1016/j.bbamcr.2011.01.026
- Kaufmann, T., Strasser, A. and Jost, P. J. 2012. Fas death receptor signalling: roles of Bid and XIAP. Cell Death Differ. 19, 42-50. https://doi.org/10.1038/cdd.2011.121
- Lee, T. K., Park, C., Jeong, S. J., Jeong, M. J., Kim, G. Y., Kim, W. J. and Choi, Y. H. 2016. Sanguinarine induces apoptosis of human oral squamous cell carcinoma KB cells via inactivation of the PI3K/Akt signaling pathway. Drug Dev. Res. 77, 227-240. https://doi.org/10.1002/ddr.21315
- Lee, J. S., Jung, W. K., Jeong, M. H., Yoon, T. R. and Kim, H. K. 2012. Sanguinarine induces apoptosis of HT-29 human colon cancer cells via the regulation of Bax/Bcl-2 ratio and caspase-9-dependent pathway. Int. J. Toxicol. 31,70-77. https://doi.org/10.1177/1091581811423845
- Li, W., Li, H., Mu, Q., Zhang, H., Yao, H., Li, J. and Niu, X. 2014. Protective effect of sanguinarine on LPS-induced endotoxic shock in mice and its effect on LPS-induced COX-2 expression and COX-2 associated PGE2 release from peritoneal macrophages. Int. Immunopharmacol. 22, 311-317. https://doi.org/10.1016/j.intimp.2014.07.017
- Matkar, S. S., Wrischnik, L. A. and Hellmann-Blumberg, U. 2008. Sanguinarine causes DNA damage and p53-independent cell death in human colon cancer cell lines. Chem. Biol. Interact. 172, 63-71. https://doi.org/10.1016/j.cbi.2007.12.006
- Miao, F., Yang, X. J., Zhou, L., Hu, H. J., Zheng, F., Ding, X. D., Sun, D. M., Zhou, C. D. and Sun, W. 2011. Structural modification of sanguinarine and chelerythrine and their antibacterial activity. Nat. Prod. Res. 25, 863-875. https://doi.org/10.1080/14786419.2010.482055
- Miller, R. A., McIver, J. E. and Gunsolley, J. C. 1988. Effects of sanguinaria extract on plaque retention and gingival health. J. Clin. Orthod. 22, 304-307.
- Nakajima, Y. I. and Kuranaga, E. 2017. Caspase-dependent non-apoptotic processes in development. Cell Death Differ. 24, 1422-1430. https://doi.org/10.1038/cdd.2017.36
- Pallichankandy, S., Rahman, A., Thayyullathil, F. and Galadari, S. 2015. ROS-dependent activation of autophagy is a critical mechanism for the induction of anti-glioma effect of sanguinarine. Free Radic. Biol. Med. 89, 708-720. https://doi.org/10.1016/j.freeradbiomed.2015.10.404
- Park, S. Y., Jin, M. L., Kim, Y. H., Lee, S. J. and Park, G. 2014. Sanguinarine inhibits invasiveness and the MMP-9 and COX-2 expression in TPA-induced breast cancer cells by inducing HO-1 expression. Oncol. Rep. 31, 497-504. https://doi.org/10.3892/or.2013.2843
- Senchina, D. S., Flinn, G. N., McCann, D. A., Kohut, M. L. and Shearn, C. T. 2009. Bloodroot (Sanguinaria canadensis L., Papaveraceae) enhances proliferation and cytokine production by human peripheral blood mononuclear cells in an in vitro model. J. Herbs Spices Med. Plants 15, 45. https://doi.org/10.1080/10496470902787485
- Slee, E. A., Zhu, H., Chow, S. C., MacFarlane, M., Nicholson, D. W. and Cohen, G. M. 1996. Benzyloxycarbonyl-Val- Ala-Asp (OMe) fluoromethylketone (Z-VAD.FMK) inhibits apoptosis by blocking the processing of CPP32. Biochem. J. 315, 21-24. https://doi.org/10.1042/bj3150021
- Tummers, B. and Green, D. R. 2017. Caspase-8: regulating life and death. Immunol. Rev. 277, 76-89. https://doi.org/10.1111/imr.12541
- Vlachojannis, C., Magora, F. and Chrubasik, S. 2012. Rise and fall of oral health products with Canadian bloodroot extract. Phytother. Res. 26, 1423-1426.
- Vrba, J., Hrbac, J., Ulrichova, J. and Modriansky, M. 2004. Sanguinarine is a potent inhibitor of oxidative burst in DMSO-differentiated HL-60 cells by a non-redox mechanism. Chem. Biol. Interact. 147, 35-37. https://doi.org/10.1016/j.cbi.2003.10.003
- Wang, Q., Dai, P., Bao, H., Liang, P., Wang, W., Xing, A. and Sun, J. 2017. Anti-inflammatory and neuroprotective effects of sanguinarine following cerebral ischemia in rats. Exp. Ther. Med. 13, 263-268. https://doi.org/10.3892/etm.2016.3947
- Yang, X. J., Miao, F., Yao, Y., Cao, F. J., Yang, R., Ma, Y. N., Qin, B. F. and Zhou, L. 2012. In vitro antifungal activity of sanguinarine and chelerythrine derivatives against phytopathogenic fungi. Molecules 17, 13026-13035. https://doi.org/10.3390/molecules171113026
- Zhang, R., Wang, G., Zhang, P. F., Zhang, J., Huang, Y. X., Lu, Y. M., Da, W., Sun, Q. and Zhu, J. S. 2017. Sanguinarine inhibits growth and invasion of gastric cancer cells via regulation of the DUSP4/ERK pathway. J. Cell. Mol. Med. 21, 1117-1127. https://doi.org/10.1111/jcmm.13043