References
- Aragane, Y., Kulms, D., Metze, D., Wilkes, G., Poppelmann, B., Luger, T.A. and Schwarz, T. (1998) UV light induces apoptosis via direct activation of CD95 (Fas/APO- 1) independently of it's ligand CD95L. J. Cell Biol., 140, 171-182. https://doi.org/10.1083/jcb.140.1.171
- Danno, K. and Horio, T. (1987) Sunburn cell: factors involved in its formation. Photochem. Photobiol., 45, 683-690. https://doi.org/10.1111/j.1751-1097.1987.tb07401.x
- Ziegler, A., Jonason, A.S., Leffell, D.J., Simon, J.A., Sharma, H.W., Kimmelman, J., Remington, L., Jacks, T. and Brash, D.E. (1994) Sunburn and p53 in the onset of skin cancer. Nature, 372, 773-776. https://doi.org/10.1038/372773a0
- Fuchs, J. and Packer, L. (1991) Photooxidative Stress in the Skin in Oxidative Stress: Oxidants and Antioxidants (Sies, H. Ed.). Academic Press, London, pp. 559-583.
- Heck, D.E., Gerecke, D.R., Vetrano, A.M. and Laskin, J.D. (2004) Solar ultraviolet radiation as a trigger of cell signal transduction. Toxicol. Appl. Pharmacol., 195, 288-297. https://doi.org/10.1016/j.taap.2003.09.028
- Banskota, A.H., Tezuka, Y. and Kadota, S. (2001) Recent progress in pharmacological research of propolis. Phytother. Res., 15, 561-571. https://doi.org/10.1002/ptr.1029
- Burdock, G.A. (1998) Review of the biological properties and toxicity of bee propolis (propolis). Food Chem. Toxicol., 36, 347-363. https://doi.org/10.1016/S0278-6915(97)00145-2
- Bankova, V. (2005) Chemical diversity of propolis and the problem of standardization. J. Ethnopharmacol., 100, 114-117. https://doi.org/10.1016/j.jep.2005.05.004
- Sforcin, J.M., Fernandes, A. Jr., Lopes, C.A., Bankova, V. and Funari, S.R. (2000) Seasonal effect on Brazilian propolis antibacterial activity. J. Ethnopharmacol., 73, 243-249. https://doi.org/10.1016/S0378-8741(00)00320-2
- Kujumgiev, A., Tsvetkova, I., Serkedjieva, Y., Bankova, V., Christov, R. and Popov, S. (1999) Antibacterial, antifungal and antiviral activity of propolis of different geographic origin. J. Ethnopharmacol., 64, 235-240. https://doi.org/10.1016/S0378-8741(98)00131-7
- Ledon, N., Casaco, A., Gonzalez, R., Merino, N., Gonzalez, A. and Tolon, Z. (1997) Antipsoriatic, anti-inflammatory, and analgesic effects of an extract of red propolis. Zhongguo Yao Li Xue Bao, 18, 274-276.
- Chen, C.N., Wu, C.L., Shy, H.S. and Lin, J.K. (2003) Cytotoxic prenylflavanones from Taiwanese propolis. J. Nat. Prod., 66, 503-506. https://doi.org/10.1021/np0203180
- Heim, K.E., Tagliaferro, A.R. and Bobilya, A.R. (2002) Flavonoid antioxidants: chemistry, metabolism and structure activity relationships. J. Nutr. Biochem., 13, 572-584. https://doi.org/10.1016/S0955-2863(02)00208-5
- Orsolic, N. and Basic, I. (2003) Immunomodulation by water-soluble derivative of propolis: a factor of antitumor reactivity. J. Ethnopharmacol., 84, 265-273. https://doi.org/10.1016/S0378-8741(02)00329-X
- Aso, K., Kanno, S., Tadano, T., Satoh, S. and Ishikawa, M. (2004) Inhibitory effect of propolis on the growth of human leukemia U937. Biol. Pharm. Bull., 27, 727-730. https://doi.org/10.1248/bpb.27.727
- Liu, G.A. and Zheng, R.L. (2002) Protection against damaged DNA in the single cell by polyphenols. Pharmazie., 57, 852-854.
- Orsolic, N., Benkovic, V., Horvat-Knezevic, A., Kopjar, N., Kosalec, I., Bakmaz, M., Mihaljevic, Z., Bendelja, K. and Basic, I. (2007) Assessment by survival analysis of the radioprotective properties of propolis and its polyphenolic compounds. Biol. Pharm. Bull., 30, 946-951. https://doi.org/10.1248/bpb.30.946
- Castaldo, S. and Capasso, F. (2002) Propolis, an old remedy used in modern medicine. Fitoterapia, 73 Suppl 1, S1-S6. https://doi.org/10.1016/S0367-326X(02)00185-5
- Simoes, L.M., Gregorio, L.E., Da Silva Filho, A.A., De Souza, M.L., Azzolini, A.E., Bastos, J.K. and Lucisano-Vlim, Y.M. (2004) Effect of Brazilian green propolis on the production of reactive oxygen species by stimulated neutrophils. J. Ethnopharmacol., 94, 59-65. https://doi.org/10.1016/j.jep.2004.04.026
- Uma Devi, P., Ganasoundari, A., Rao, B.S. and Srinivasan, K.K. (1999) In vivo radioprotection by ocimum flavonoids: survival of mice. Radiat. Res., 151, 74-78. https://doi.org/10.2307/3579750
- Arora, R., Chawla, R., Puri, S.C., Sagar, R., Singh, S., Kumar, R., Sharma, A.K., Prasad, J., Singh, S., Kaur, G., Chaudhary, P., Qazi, G.N. and Sharma, R.K. (2005) Radioprotective and antioxidant properties of low-altitude Podophyllum hexandrum (LAPH). J. Environ. Pathol. Toxicol. Oncol., 24, 299-314. https://doi.org/10.1615/JEnvironPatholToxicolOncol.v24.i4.70
- Benkovic, V., Horvat Knezevic, A., Brozovic, G., Knezevic, F., Dikic, D., Bevanda, M., Basic, I. and Orsolic, N. (2007) Enhanced antitumor activity of irinotecan combined with propolis and its polyphenolic compounds on Ehrlich ascites tumor in mice. Biomed. Pharmacother., 61, 292-297. https://doi.org/10.1016/j.biopha.2007.02.012
- Benkovic, V., Knezevic, A.H., Dikic, D., Lisicic, D., Orsolic, N., Basic, I., Kosalec, I. and Kopjar, N. (2008) Radioprotective effects of propolis and quercetin in c-irradiated mice evaluated by the alkaline comet assay. Phytomedicine, 15, 851-858. https://doi.org/10.1016/j.phymed.2008.02.010
- Lu, Y.Y., Chen, T.S., Wang, X.P., Qu, J.L. and Chen, M. (2010) The JNK inhibitor SP600125 enhances dihydroartemisinin-induced apoptosis by accelerating Bax translocation into mitochondria in human lung adenocarcinoma cells. FEBS Lett., 584, 4019-4026. https://doi.org/10.1016/j.febslet.2010.08.014
- Shin, D.Y., Kim, G.Y., Li, W., Choi, B.T., Kim, N.D., Kang, H.S. and Choi, Y.H. (2009) Implication of intracellular ROS formation, caspase-3 activation and Egr-1 induction in platycodon D-induced apoptosis of U937 human leukemia cells. Biomed. Pharmacother., 63, 86-94. https://doi.org/10.1016/j.biopha.2008.08.001
- Zoratti, M. and Szabo, I. (1995) The mitochondrial permeability transition. Biochim. Biophys. Acta, 1241, 139-176. https://doi.org/10.1016/0304-4157(95)00003-A
- Vander Heiden, M.G., Chandel, N.S., Williamson, E.K., Schumacker, P.T. and Thompson, C.B. (1997) Bcl-xL regulates the membrane potential and volume homeostasis of mitochondria. Cell, 91, 627-637. https://doi.org/10.1016/S0092-8674(00)80450-X
- Fiers, W., Beyaert, R., Declercq, W. and Vandenabeele, P. (1999) More than one way to die: apoptosis, necrosis and reactive oxygen damage. Oncogene, 18, 7719-7730. https://doi.org/10.1038/sj.onc.1203249
- Fleury, C., Mignotte, B. and Vayssiere, J.L. (2002) Mitochondrial reactive oxygen species in cell death signaling. Biochimie, 84, 131-141. https://doi.org/10.1016/S0300-9084(02)01369-X
- Chakraborti, T., Das, S., Mondal, M., Roychoudhury, S. and Chakraborti, S. (1999) Oxidant, mitochondria and calcium: an overview. Cell. Signal., 1, 77-85.
- Garssen, J., van Steeg, H., de Gruijl, F., de Boer, J., van der Horst, G.T., van Kranen, H., van Loveren, H., van Dijk, M., Fluitman, A., Weeda, G. and Hoeijmakers, J.H. (2000) Transcription coupled and global genome repair differentially influence UV-B-induced acute skin effects and systemic immunosuppression. J. Immunol., 164, 6199-6205. https://doi.org/10.4049/jimmunol.164.12.6199
- Wenk, J., Brenneisen, P., Meewes, C., Wlaschek, M., Peters, T., Blaudschun, R., Ma, W., Kuhr, L., Schneider, L. and Scharffetter-Kochanek, K. (2001) UV-induced oxidative stress and photoaging. Curr. Probl. Dermatol., 29, 83-94.
- Kulms, D., Zeise, E., Poppelmann, B. and Schwarz, T. (2002) DNA damage, death receptor activation and reactive oxygen species contribute to ultraviolet radiation induced apoptosis in an essential and independent way. Oncogene, 21, 5844-5851. https://doi.org/10.1038/sj.onc.1205743
- Chen, Y.C., Lin-Shiau, S.Y. and Lin, J.K. (1998) Involvement of reactive oxygen species and caspase 3 activation in arsenite-induced apoptosis. J. Cell. Physiol., 177, 324-333. https://doi.org/10.1002/(SICI)1097-4652(199811)177:2<324::AID-JCP14>3.0.CO;2-9
- Irani, K. (2000) Oxidant signaling in vascular cell growth, death, and survival: a review of the roles of reactive oxygen species in smooth muscle and endothelial cell mitogenic and apoptotic signaling. Circ. Res., 87, 179-183. https://doi.org/10.1161/01.RES.87.3.179
- Moreno, M.I.N., Isla, M.I., Sampietro, A.R. and Vattuone, M.A. (2000) Comparison of the free radical-scavenging activity of propolis from several regions of Argentina. J. Ethnopharmacol., 71,109-114. https://doi.org/10.1016/S0378-8741(99)00189-0
- Kumazawa, S., Hamasaka, T. and Nakayama, T. (2004) Antioxidant activity of propolis of various geographic origins. Food Chem., 84, 329-339. https://doi.org/10.1016/S0308-8146(03)00216-4
- Banskota, A.H., Tezuka, Y., Adnyana, I.K., Ishii, E., Midorikawa, K., Matsushige, K. and Kadota, S. (2001) Hepatoprotective and anti-Helicobacter pylori activities of constituents from Brazilian propolis. Phytomedicine, 8, 16-23. https://doi.org/10.1078/0944-7113-00004
- Mohammadzadeh, S., Sharriatpanahi, M., Hamedi, M., Amanzadeh, Y., Ebrahimi, S.E.S. and Ostad, S.N. (2007) Antioxidant power of Iranian propolis extract. Food Chem., 103, 729-733. https://doi.org/10.1016/j.foodchem.2006.09.014
- Chiao, C., Carothers, A.M., Grunberger, D., Solomon, G., Preston, A.G. and Barrett, C.J. (1995) Apoptosis and altered redox state induced by caffeic acid phenethyl ester (CAPE) in transformed rat fibroblast cells. Cancer Res., 55, 3576-3583.
- Rao, C.V., Desai, D., Rivenson, A., Simi, B., Amin, S. and Reddy, S.B. (1995) Chemoprevention of colon carcinogenesis by phenylethyl-3-methylcaffeate. Cancer Res., 55, 2310-2315.
- Xuan, H., Zhao, J., Miao, J., Li, Y., Chu, Y. and Hu, F. (2011) Effect of Brazilian propolis on human umbilical vein endothelial cell apoptosis. Food Chem. Toxicol., 49, 78-85. https://doi.org/10.1016/j.fct.2010.09.034
- Eom, H.S., Lee, E.J., Yoon, B.S. and Yoo, B.S. (2010) Propolis inhibits the proliferation of human leukaemia HL-60 cells by inducing apoptosis through the mitochondrial pathway. Nat. Prod. Res., 24, 375-386. https://doi.org/10.1080/14786410903370908
- Chen, C.N., Wu, C.L. and Lin, J.K. (2007) Apoptosis of human melanoma cells induced by the novel compounds propolin A and propolin B from Taiwenese propolis. Cancer Lett., 245, 218-231. https://doi.org/10.1016/j.canlet.2006.01.016
- Ishihara, M., Naoi, K., Hashita, M., Itoh, Y. and Suzui, M. (2009) Growth inhibitory activity of ethanol extract of Chinese and Brazilian propolis in four human colon carcinoma cell lines. Oncol. Rep., 22, 349-354.
- Huang, W.J., Huang, C.H., Wu, C.L., Lin, J.K., Chen, Y.W., Lin, C.L., Chuang, S.E., Huang, C.Y. and Chen, C.N. (2007) Propolin G, a prenylflavanone, isolated from Taiwanese propolis, induces caspase-dependent apoptosis in brain cancer cells. J. Agric. Food Chem., 55, 7366-7376. https://doi.org/10.1021/jf0710579
- Weng, M.S., Liao, C.H., Chen, C.N., Wu, C.L. and Lin, J.K. (2007) Propolin H. from Taiwanese propolis induces G1 arrest in human lung carcinoma cells. J. Agric. Food Chem., 55, 5289-5298. https://doi.org/10.1021/jf070201n
- Sforcin, J.M. (2007) Propolis and the immune system: a review. J. Ethnopharmacol., 113, 1-14. https://doi.org/10.1016/j.jep.2007.05.012
- Moon, J.Y., Lee, E.J. and Yoo, B.S. (2012) Propolis Protects Human Keratinocyte HaCaT Cells against UV-induced Apoptosis. Journal of Apiculture, 27, 243-249.
- Tavares, D.C., Mazzaron Barcelos, G.R., Silva, L.F., Chacon Tonin, C.C. and Bastos, J.K. (2006) Propolis-induced genotoxicity and antigenotoxicity in Chinese hamster ovary cells. Toxicol. In Vitro, 20, 1154-1158. https://doi.org/10.1016/j.tiv.2006.02.009
Cited by
- 3-Bromo-4,5-dihydroxybenzaldehyde Enhances the Level of Reduced Glutathione via the Nrf2-Mediated Pathway in Human Keratinocytes vol.15, pp.9, 2017, https://doi.org/10.3390/md15090291
- RIP1-dependent reactive oxygen species production executes artesunate-induced cell death in renal carcinoma Caki cells vol.435, pp.1-2, 2017, https://doi.org/10.1007/s11010-017-3052-7
- Luteolin induces apoptotic cell death via antioxidant activity in human colon cancer cells vol.51, pp.4, 2017, https://doi.org/10.3892/ijo.2017.4091
- Risk management of free radicals involved in air travel syndromes by antioxidants vol.21, pp.2, 2018, https://doi.org/10.1080/10937404.2018.1427914
- Proteomic Changes in Chick Brain Proteome Post Treatment with Lathyrus Sativus Neurotoxin, β-N-Oxalyl-L-α,β-Diaminopropionic Acid (L-ODAP): A Better Insight to Transient Neurolathyrism vol.34, pp.3, 2018, https://doi.org/10.5487/TR.2018.34.3.267
- Particulate matter 2.5 damages skin cells by inducing oxidative stress, subcellular organelle dysfunction, and apoptosis vol.92, pp.6, 2018, https://doi.org/10.1007/s00204-018-2197-9
- Induction of Apoptosis by Citrus unshiu Peel in Human Breast Cancer MCF-7 Cells: Involvement of ROS-Dependent Activation of AMPK vol.41, pp.5, 2018, https://doi.org/10.1248/bpb.b17-00898
- peel in MDA-MB-231 human breast carcinoma cells vol.12, pp.2, 2018, https://doi.org/10.4162/nrp.2018.12.2.129
- Natural Antioxidants: Multiple Mechanisms to Protect Skin From Solar Radiation vol.9, pp.1663-9812, 2018, https://doi.org/10.3389/fphar.2018.00392
- Dihydrocaffeic Acid Prevents UVB-Induced Oxidative Stress Leading to the Inhibition of Apoptosis and MMP-1 Expression via p38 Signaling Pathway vol.2019, pp.1942-0994, 2019, https://doi.org/10.1155/2019/2419096