DOI QR코드

DOI QR Code

6,8-Dihydroxy-7-methoxy-1-methyl-azafluorenone Induces Caspase-8- and -9-mediated Apoptosis in Human Cancer Cells

  • Published : 2013.04.30

Abstract

6,8-Dihydroxy-7-methoxy-1-methyl-azafluorenone (DMMA), a purified compound from Polyalthia cerasoides roots, is cytotoxic to various cancer cell lines. The aims of this study were to demonstrate the type of cancer cell death and the mechanism(s) involved. DMMA inhibited cell growth and induced apoptotic death in human leukemic cells (HL-60, U937, MOLT-4), human breast cancer MDA-MB231 cells and human hepatocellular carcinoma HepG2 cells in a dose dependent manner, with $IC_{50}$ values ranging between 20-55 ${\mu}M$. DMMA also decreased cell viability of human peripheral blood mononuclear cells. The morphology of cancer cells induced by the compound after staining with propidium iodide and examined under a fluorescence microscope was condensed nuclei and apoptotic bodies. Mitochondrial transmembrane potential (MTP) was decreased after 24h exposure in all five types of cancer cells. DMMA-induced caspase-3, -8, and -9 activity was strongly induced in human leukemic HL-60 and MOLT-4 cells, while in U937-, MDA-MB231- and HepG2-treated cells there was partial induction of caspase. In conclusion, DMMA-induced activation of caspase-8 and -9 resulted in execution of apoptotic cell death in human leukemic HL-60 and MOLT-4 cell lines via extrinsic and intrinsic pathways.

Keywords

References

  1. Ashkenazi A (2008). Targeting the extrinsic apoptosis pathway in cancer. Cytokine Growth Factor Rev, 19, 325-31. https://doi.org/10.1016/j.cytogfr.2008.04.001
  2. Banjerdpongchai R, Kongtawelert P, Khantamat O, et al (2010a). Mitochondrial and endoplasmic reticulum stress pathways cooperate in zearalenone-induced apoptosis of human leukemic cells. J Hematol Oncol, 3, 50-65. https://doi.org/10.1186/1756-8722-3-50
  3. Banjerdpongchai R, Punyati P, Nakrob A, Pompimon W, Kongtawelert P (2011). 4'-Hydroxycinnamaldehyde from Alpinia galanga (Linn.) induces human leukemic cell apoptosis via mitochondrial and endoplasmic reticulum stress pathways. Asian Pac J Cancer Prev. 12, 593-8.
  4. Banjerdpongchai R, Yingyurn S, Kongtawelert P (2010b). Sesamin induces human leukemic cell apoptosis via mitochondrial and endoplasmic reticulum stress pathways. World J Oncol. 1, 78-86.
  5. Clarke N, Germain P, Altucci L, Gronemeyer H (2004). Retinoids: potential in cancer prevention and therapy. Expert Rev Mol Med. 6, 1-23.
  6. Faucheu C, Diu A, Chan AW, et al (1995). A novel human protease similar to the interleukin-1 beta converting enzyme induces apoptosis in transfected cells. EMBO J. 14, 1914-22.
  7. Gewies A (2003). Introduction to apoptosis. ApoReview. 1002, 1-6.
  8. Ghobrial IM, Witzig TE, Adjei AA (2005). Targeting apoptosis pathways in cancer therapy. CA Cancer J Clin. 55, 178-94. https://doi.org/10.3322/canjclin.55.3.178
  9. Henshall DC, Chen J, Simon RP (2000). Involvement of caspase-3-like protease in the mechanism of cell death following focally evoked limbic seizures. J Neurochem. 74, 1215-23. https://doi.org/10.1046/j.1471-4159.2000.741215.x
  10. Jemal A, Bray F, Center MM, et al (2011). Global cancer statistics. CA Cancer J Clin. 61, 69-90. https://doi.org/10.3322/caac.20107
  11. Kanokmedhakul S, Kanokmedhakul K, Lekphrom R (2007). Bioactive constituents of the roots of Polyalthia cerasoides. J Nat Prod. 70, 1536-8. https://doi.org/10.1021/np070293a
  12. Koschny R, Ganten TM, Sykora J, et al (2007). TRAIL/ bortezomib cotreatment is potentially hepatotoxic but induces cancer-specific apoptosis within a therapeutic window. Hepatology. 45, 649-58. https://doi.org/10.1002/hep.21555
  13. LaVallee TM, Zhan XH, Johnson MS, et al (2003). 2-methoxyestradiol up-regulates death receptor 5 and induces apoptosis through activation of the extrinsic pathway. Cancer Res. 63, 468-75.
  14. Liu Y, Borchert GL, Surazynski A, Hu CA, Phang JM (2006). Proline oxidase activates both intrinsic and extrinsic pathways for apoptosis: the role of ROS/superoxides, NFAT and MEK/ERK signaling. Oncogene. 25, 5640-7. https://doi.org/10.1038/sj.onc.1209564
  15. Marchetti C, Obert G, Deffosez A, Formstecher P, Marchetti P (2002). Study of mitochondrial membrane potential, reactive oxygen species, DNA fragmentation and cell viability by flow cytometry in human sperm. Hum Reprod. 17, 1257-65. https://doi.org/10.1093/humrep/17.5.1257
  16. Padma P, Chansouria JP, Khosa RL (1999). Hepatoprotective activity of Annona muricata Linn. and Polyalthia cerasoides bedd. Anc Sci Life. 19, 7-10.
  17. Pumsalid K, Thaisuchat H, Loetchutinat C, et al (2010). A new azafluorenone from the roots of Polyalthia cerasoides and its biological activity. Nat Prod Commun. 5, 1931-4.
  18. Ravikumar YS, Mahadevan KM, Kumaraswamy MN, et al (2008). Antioxidant, cytotoxic and genotoxic evaluation of alcoholic extract of Polyalthia cerasoides (Roxb.) Bedd. Environ Toxicol Pharmacol. 26, 142-6. https://doi.org/10.1016/j.etap.2008.03.001
  19. Ravikumar YS, Mahadevan KM, Manjunatha H, Satyanarayana ND (2010). Antiproliferative, apoptotic and antimutagenic activity of isolated compounds from Polyalthia cerasoides seeds. Phytomedicine. 17, 513-8. https://doi.org/10.1016/j.phymed.2009.09.005
  20. Siegel R, Naishadham D, Jemal A (2012). Cancer statistics, 2012. CA Cancer J Clin. 62, 10-29. https://doi.org/10.3322/caac.20138
  21. Yanase N, Ohshima K, Ikegami H, Mizuguchi J (2000). Cytochrome c release, mitochondrial membrane depolarization, caspase-3 activation, and Bax-alpha cleavage during IFN-alpha-induced apoptosis in Daudi B lymphoma cells. J Interferon Cytokine Res. 20, 1121-9. https://doi.org/10.1089/107999000750053799

Cited by

  1. Synthesis of substituted azafluorenones from dihalogeno diaryl ketones by palladium-catalyzed auto-tandem processes vol.12, pp.41, 2014, https://doi.org/10.1039/C4OB01629G
  2. Fenofibrate Increases Radiosensitivity in Head and Neck Squamous Cell Carcinoma via Inducing G2/M Arrest and Apoptosis vol.15, pp.16, 2014, https://doi.org/10.7314/APJCP.2014.15.16.6649
  3. Enterocarpam-III Induces Human Liver and Breast Cancer Cell Apoptosis via Mitochondrial and Caspase-9 Activation vol.16, pp.5, 2015, https://doi.org/10.7314/APJCP.2015.16.5.1833
  4. An appropriate one-pot synthesis of 4-aryl-2-naphthalen-2-yl-5H-indeno [1,2-b]pyridin-5-ones using thiourea dioxide as an efficient and reusable organocatalyst vol.41, pp.9, 2015, https://doi.org/10.1007/s11164-014-1742-2
  5. Access toward Fluorenone Derivatives through Solvent-Free Ruthenium Trichloride Mediated [2 + 2 + 2] Cycloadditions vol.18, pp.21, 2016, https://doi.org/10.1021/acs.orglett.6b02840