DAW22, a natural sesquiterpene coumarin isolated from Ferula ferulaeoides (Steud.) Korov. that induces C6 glioma cell apoptosis and endoplasmic reticulum (ER) stress

Fitoterapia

Volumn 103, Issue , 2015, Pages 46-54

  Zhang, Lan ^a   Tong, Xupeng ^b   Zhang, Jin ^a   Huang, Jian ^a   Wang, Jinhui ^a,c  

^a SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

^b CHINA PHARMACEUTICAL UNIVERSITY   (China)

^c SHIHEZI UNIVERSITY   (China)

Author keywords

Apoptosis; C6 glioma cell; DAW22; Endoplasmic reticulum (ER) stress; Ferula ferulaeoides (Steud.) Korov.

Indexed keywords

ACTIVATING TRANSCRIPTION FACTOR 6; ANTINEOPLASTIC AGENT; CASPASE 12; CASPASE 8; COUMARIN DERIVATIVE; DAW 22; PROTEIN BCL 2; PROTEIN IRE1; SESQUITERPENE DERIVATIVE; UNCLASSIFIED DRUG; COUMARIN; SESQUITERPENE;

APOPTOSIS; ARTICLE; CELL VACUOLE; CONTROLLED STUDY; DOWN REGULATION; ENDOPLASMIC RETICULUM STRESS; ENZYME ACTIVATION; ENZYME PHOSPHORYLATION; FERULA; FERULA FERULAEOIDES; GLIOMA CELL; MITOCHONDRIAL MEMBRANE POTENTIAL; NONHUMAN; PRIORITY JOURNAL; PROTEIN CLEAVAGE; SIGNAL TRANSDUCTION; ANIMAL; CHEMISTRY; DRUG EFFECTS; GLIOMA; MOLECULAR DOCKING; MOUSE; PATHOLOGY; PLANT ROOT; TUMOR CELL LINE; UNFOLDED PROTEIN RESPONSE;

FERULA FERULOIDES;

ANIMALS; APOPTOSIS; CELL LINE, TUMOR; COUMARINS; ENDOPLASMIC RETICULUM STRESS; FERULA; GLIOMA; MICE; MOLECULAR DOCKING SIMULATION; PLANT ROOTS; SESQUITERPENES; UNFOLDED PROTEIN RESPONSE;

EID: 84925441663     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2015.03.010     Document Type: Article

References (39)

1. P.U. Kumthekar, B.D. Macrie, S.K. Singh, G. Kaur, J.P. Chandler, and S.V. Sejpal A review of management strategies of malignant gliomas in the elderly population Am J Cancer Res 4 2014 436 444
2. R. Stupp, W.P. Mason, M.J. van den Bent, M. Weller, B. Fisher, and M.J. Taphoorn Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma N Engl J Med 352 2005 987 996
3. L.L. Fu, Y. Yang, H.L. Xu, Y. Cheng, X. Wen, and L. Ouyang Identification of novel caspase/autophagy-related gene switch to cell fate decisions in breast cancers Cell Prolif 46 2013 67 75
4. S. Elmore Apoptosis: a review of programmed cell death Toxicol Pathol 35 2007 495 516
5. R.W. Johnstone, A.A. Ruefli, and S.W. Lowe Apoptosis: a link between cancer genetics and chemotherapy Cell 108 2002 153 164
6. S. Cory, and J.M. Adams Killing cancer cells by flipping the Bcl-2/Bax switch Cancer Cell 8 2005 5 6
7. M. Kurokawa, and S. Kornbluth Caspases and kinases in a death grip Cell 138 2009 838 854
8. R.V. Rao, H.M. Ellerby, and D.E. Bredesen Coupling endoplasmic reticulum stress to the cell death program Cell Death Differ 11 2004 372 380
9. A.H. Schönthal Endoplasmic reticulum stress: its role in disease and novel prospects for therapy Scientifica (Cairo) 2012 2012 857516
10. W.A. Wang, J. Groenendyk, and M. Michalak Endoplasmic reticulum stress associated responses in cancer Biochim Biophys Acta 2014 1843 2143 2149
11. A. Chakrabarti, A.W. Chen, and J.D. Varner A review of the mammalian unfolded protein response Biotechnol Bioeng 108 2011 2777 2793
12. A.M. Gorman, S.J. Healy, R. Jäger, and A. Samali Stress management at the ER: regulators of ER stress-induced apoptosis Pharmacol Ther 134 2012 306 316
13. H. Urra, E. Dufey, F. Lisbona, D. Rojas-Rivera, and C. Hetz When ER stress reaches a dead end Biochim Biophys Acta 2013 1833 3507 3517
14. F. Martinon Targeting endoplasmic reticulum signaling pathways in cancer Acta Oncol 51 2012 822 830
15. G.C. Shore, F.R. Papa, and S.A. Oakes Signaling cell death from the endoplasmic reticulum stress response Curr Opin Cell Biol 23 2011 143 149
16. I. Tabas, and D. Ron Integrating the mechanisms of apoptosis induced by endoplasmic reticulum stress Nat Cell Biol 13 2011 184 190
17. T. Nakagawa, H. Zhu, N. Morishima, E. Li, J. Xu, and B.A. Yankner Caspase-12 mediates endoplasmic-reticulum-specific apoptosis and cytotoxicity by amyloid-beta Nature 403 2000 98 103
18. G.G. Johnson, M.C. White, and M. Grimaldi Stressed to death: targeting endoplasmic reticulum stress response induced apoptosis in gliomas Curr Pharm Des 17 2011 284 292
19. H. Meng, G.Y. Li, J. Huang, K. Zhang, H.Y. Wang, and J.H. Wang Sesquiterpene coumarin and sesquiterpene chromone derivatives from Ferula ferulaeoides (Steud.) Korov. Fitoterapia 86 2013 70 77
20. K. Isaka, A. Nagatsu, P. Ondognii, O. Zevgeegiin, P. Gombosurengyin, and K. Davgiin Sesquiterpenoid derivatives from Ferula ferulioides V. Chem. Pharm. Bull. (Tokyo) 49 2001 1072 1076
21. Y. Cheng, F. Qiu, Y.C. Ye, Z.M. Guo, S. Tashiro, and S. Onodera Autophagy inhibits reactive oxygen species-mediated apoptosis via activating p38-nuclear factor-kappa B survival pathways in oridonin-treated murine fibrosarcoma L929 cells FEBS J 276 2009 1291 1306
22. M.J. Keiser, B.L. Roth, B.N. Armbruster, P. Ernsberger, J.J. Irwin, and B.K. Shoichet Relating protein pharmacology by ligand chemistry Nat Biotechnol 25 2007 197 206
23. K. Yoshida Role for DYRK family kinases on regulation of apoptosis Biochem Pharmacol 76 2008 1389 1394
24. C. Tang, H. Xue, H. Huang, and X.G. Wang Tanshinone IIA inhibits constitutive STAT3 activation, suppresses proliferation, and induces apoptosis in rat C6 glioma cells Neurosci Lett 470 2010 126 129
25. X. Guo, J.G. Williams, T.T. Schug, and X. Li DYRK1A and DYRK3 promote cell survival through phosphorylation and activation of SIRT1 J Biol Chem 285 2010 13223 13232
26. W. Becker, and W. Sippl Activation, regulation, and inhibition of DYRK1A FEBS J 278 2011 246 256
27. L. Lim, V. Jackson-Lewis, L.C. Wong, G.H. Shui, A.X. Goh, and S. Kesavapany Lanosterol induces mitochondrial uncoupling and protects dopaminergic neurons from cell death in a model for Parkinson's disease Cell Death Differ 19 2011 416 427
28. C.H. Jakobsen, G.L. Størvold, H. Bremseth, T. Follestad, K. Sand, and M. Mack DHA induces ER stress and growth arrest in human colon cancer cells: associations with cholesterol and calcium homeostasis J Lipid Res 49 2008 2089 2100
29. L. Qin, Z. Wang, L. Tao, and Y. Wang ER stress negatively regulates AKT/TSC/mTOR pathway to enhance autophagy Autophagy 6 2010 239 247
30. P.L. Faust, and W.J. Kovacs Cholesterol biosynthesis and ER stress in peroxisome deficiency Biochimie 98 2014 75 85
31. L. Guan, B. Han, J. Li, Z. Li, F. Huang, and Y. Yang Exposure of human leukemia NB4 cells to increasing concentrations of selenite switches the signaling from pro-survival to pro-apoptosis Ann Hematol 88 2009 733 742
32. L. Pan, H.B. Chai, and A.D. Kinghorn Discovery of new anticancer agents from higher plants Front Biosci (Schol Ed) 4 2012 142 156
33. S. Shen, Y. Zhang, Z. Wang, R. Liu, and X. Gong Bufalin induces the interplay between apoptosis and autophagy in glioma cells through endoplasmic reticulum stress Int J Biol Sci 10 2014 212 224
34. Y.C. Chang, F.P. Chou, H.P. Huang, J.D. Hsu, and C.J. Wang Inhibition of cell cycle progression by penta-acetyl geniposide in rat C6 glioma cells Toxicol Appl Pharmacol 198 2004 11 20
35. J.Y. Sun, H. Yang, S. Miao, J.P. Li, S.W. Wang, and M.Z. Zhu Suppressive effects of swainsonine on C6 glioma cell in vitro and in vivo Phytomedicine 16 2009 1070 1074
36. L. Lv, L. Zheng, D. Dong, L. Xu, L. Yin, and Y. Xu Dioscin, a natural steroid saponin, induces apoptosis and DNA damage through reactive oxygen species: a potential new drug for treatment of glioblastoma multiforme Food Chem Toxicol 59 2013 657 669
37. Z.E. Nazari, and M. Iranshahi Biologically active sesquiterpene coumarins from Ferula species Phytother Res 25 2011 315 323
38. O. Gholami, M. Jeddi-Tehrani, M. Iranshahi, A.H. Zarnani, and S.A. Ziai Umbelliprenin from Ferula szowitsiana activates both intrinsic and extrinsic pathways of apoptosis in Jurkat T-CLL cell line Iran J Pharm Res 12 2013 371 376
39. G.Y. Zhu, Y.W. Li, A.K. Tse, D.K. Hau, C.H. Leung, and Z.L. Yu 20(S)-Protopanaxadiol, a metabolite of ginsenosides, induced cell apoptosis through endoplasmic reticulum stress in human hepatocarcinoma HepG2 cells Eur J Pharmacol 668 2011 88 98