Triptolide sensitizes lung cancer cells to TNF-related apoptosis-inducing ligand (TRAIL)-induced apoptosisby inhibition of NF-${kappa}B$ activation

Lee, Kye-Young;Park, Jae-Seuk;Jee, Young-Koo;Rosen, Glenn D.

  • Published : 2002.12.31

Abstract

TNF-related apoptosis-inducing ligand (TRAIL/Apo-2L), a newly identified member of the TNF family promotes apoptosis by binding to the transmembrane receptors (TRAIL-R1/DR4 and TRAIL-R2/DR5). TRAIL known to activate $NF-{\kappa}B$ in number of tumor cells including A549 (wt p53) and NCI-H1299 (null p53) lung cancer cells exerts relatively selective cytotoxic affects to the human tumor cell lines without much effect on the normal cells. We set out to identify an agent that would sensitize lung cancer cells to TRAIL-induced apoptosis through inhibition of $NF-{\kappa}B$ activation. We found that triptolide, an oxygenated diterpene extracted and purified from the Chinese herb Tripterygium wilfordii sensitized A549 and NCI-H1299 cells to TRAIL-induced apoptosis through inhibition of $NF-{\kappa}B$ activation. Pretreatment with MG132 which is a well-known $NF-{\kappa}B$ inhibitor by blocking degradation of $I{\kappa}B{\alpha}$ also greatly sensitized lung cancer cells to TRAIL-induced apoptosis. Triptolide did not block DNA binding of $NF-{\kappa}B$ activated by TRAIL as in the case of $TNF-{\alpha}$. It has been already proven that triptolide blocks transactivation of p65 which plays a key role in $NF-{\kappa}B$ activation. These observations suggest that triptolide may be a potentially useful drug to enhance TRAIL-induced tumor killing in lung cancer.

Keywords

References

  1. Na Med v.2 Specific p53 mutations are associated with de novo resistance to doxorubicin in breastcancer patients Aas, T.;Bborresen, A.L.;Geisler, S.;Smith-Sorensen, B.;Johnsen, H.;Varhaug, J.E.;Akslen, L.A.;Lonning, P.A. https://doi.org/10.1038/nm0796-811
  2. Science v.281 Death receptors: signaling and modulation Ashkenazi, A.;Dixit, V.M. https://doi.org/10.1126/science.281.5381.1305
  3. Science v.274 An essential role for NF-kappaB in preventing TNF-alpha-induced cell death Beg, A.A.;Baltimore, D. https://doi.org/10.1126/science.274.5288.782
  4. Immunity v.7 Death receptor 5, a new mwmber of the TNFR family, and DR4 induce FADD-dependent apoptosis and activate the NF-$\kappa$B pathway Chaudhary, P.M.;Eby, M.;Jasmin, A.;Bookwalter, A.;Murray, J.;Hood, L. https://doi.org/10.1016/S1074-7613(00)80400-8
  5. Cancer Res v.54 Induction of chemosensitivity in human lung cancer cells in vivo by adenovirus-mediated transfer of the wild-type p53 gene Fujiwara, T.E.;Grimm, A.;Mukhopadhyay, T.;Zhang, W.W.;OwenSchaub, L.B.;Roth, J.A.
  6. J Biol Chem v.272 p53-dependent induction of apoptosis by proteosome inhibitors Gazos Lopez, U.;Erhardt, P.;Yao, R.;Cooper, G.M. https://doi.org/10.1074/jbc.272.20.12893
  7. Curr Opin Immunol v.10 TRAIL: a molecule with multiple receptors and control Griffith, T.S.;Lynch, D.H. https://doi.org/10.1016/S0952-7915(98)80224-0
  8. J Immunol v.161 Intracellular regulation of TRAIL-induced apoptosis in human melanoma cells Griffith, T.S.;Chin, W.A.;Jackson, G.C.;Lynch, D.H.;Kubin, M.l.
  9. Blood v.91 Inhibition of nuclear factor $\kappa$B activation attenuates apoptosis resistance in lymphoid cells Jeremias, I.;Kupatt, C.;Baumann, B.;Herr, I.;Wirth, T.;Debatin, K.M.
  10. Cancer Res v.59 Chemotherapy augments TRAIL-induced apoptosis in breast cancer cell lines Keane, M.M.;Ettenberg, S.A.;Nau, M.M.;Russel, E.K.;Lipkowitz, S.
  11. J Am Chem Soc v.94 Triptolide and tripdiolide, novel antileukemic diterpenoid triepoxides from Tripterygium wilfordii Kupchan, S.M.;Court, W.A.;Dailey, R.G. Jr.;Gilmore, C.J.;Bryan, R.F. https://doi.org/10.1021/ja00775a078
  12. Gene Anal Tech v.5 A small-scale procedure for preparation of nuclear extracts that support efficient transcription and pre-mRNA splicing Lee, K.A.;Binderreif, A.;Green, M.R. https://doi.org/10.1016/0735-0651(88)90023-4
  13. J Biol Chem v.274 PG490 (triptolide) cooperates with tumor necrosis factor-$\alpha$ to induce apoptosis in tumor cells Lee, K.Y.;Chang, W.T.;Qiu, D.;Kao, P.N.;Rosen, G.D. https://doi.org/10.1074/jbc.274.19.13451
  14. Cell v.88 p53, the cellular gatekeeper for growth and division Levine, A.J. https://doi.org/10.1016/S0092-8674(00)81871-1
  15. Cell v.74 p53-Dependent apoptosis modulates the cytotoxicity of anticancer agents Lowe, S.W.;Ruley, H.E.;Jacks, T.;Houseman, D.E. https://doi.org/10.1016/0092-8674(93)90719-7
  16. Cell v.88 Apoptosis by death factor Nagata, S. https://doi.org/10.1016/S0092-8674(00)81874-7
  17. Cell v.78 The ubiquitin-proteasome pathway is required for processing the NF-kappa-B1 precursor protein and the activation of NFkappa-B Palombella, V.J.;Rando, O.J.;Goldberg, A.L.;Maniatis, T. https://doi.org/10.1016/S0092-8674(94)90482-0
  18. Science v.277 An antagonist decoy receptor and a death domain-containing receptor for TRAIL Pan, G.;Ni, J.;Wei, Y.F.;Yu, G.;Gentz, R.;Dixit, V.M. https://doi.org/10.1126/science.277.5327.815
  19. Science v.276 The receptor for the cytotoxic ligand TRAIL Pan, G.;Orourke, K.;Chinnaiyan, A.M.;Gentz, R.;Ebner, R.;Ni, J.;Dixit, V.M. https://doi.org/10.1126/science.276.5309.111
  20. J Biol Chem v.271 Induction of apoptosis by Apo-2 ligand, a new member of the tumor necrosis factor cytokine family Pitti, R.M.;Marsters, S.A.;Ruppert, S.;Donahue, C.J.;Moore, A.;Ashkenazi, A. https://doi.org/10.1074/jbc.271.22.12687
  21. J Biol Chem v.274 Immunosuppressant PG490 (triptolide) inhibits T-cell interleukin-2 expression at the level of purine-box/nuclear factor of activated T-cells and NF-$\kappa$B transcriptional activation Qiu, D.;Zhao, G.;Aoki, Y.;Shi, l.;Uyei, A.;Nazarian, S.;Kao, P.N. https://doi.org/10.1074/jbc.274.19.13443
  22. J Biol Chem v.269 An intricate arrangement of binding sites for the Ets family of transcription factors regulates activity of the alpha 4 integrin gene promoter Rosen, G.D.;Barks, J.l.;lademarco, M.F.;Fisher, R.J.;Dean, D.C.
  23. Cancer lett v.112 Evaluation of the mutagenic, cytotoxic, and antitumor potential of triptolide, a highly oxygenated diterpene isolated from Tripterygium wilfordii Shamon, L.A.(et al.) https://doi.org/10.1016/S0304-3835(96)04554-5
  24. Science v.277 Control of TRAlL-induced apoptosis by a family of signaling and decoy receptors Sheridan, J.P.;Marsters, S.A.;Pitti, R.M.;Gurney, A.;Skubatch, M.;Baldwin, D.;Ramakrishnan, L.;Gray, C.l.;Baker, K.;Wood, W.I.;Goddard, A.D.;Godowski, P.;Ashkenazi, A. https://doi.org/10.1126/science.277.5327.818
  25. Biochem J v.317 Apoptosis induction resulting from protease inhibition Shinohara, K.;Tomioka, M.;Nakano, H.;Tone, S.;Ito, H.;Kawashima, S. https://doi.org/10.1042/bj3170385
  26. Cell v.76 The TNF-receptor superfamily of cellular and viral proteins: Activation, costimulation, and death Smith, C.A.;Farrah, T.;Goodwin, R.G.
  27. J Pharmacol Exp Ther v.272 The identity of immunosuppressive components of the ethyl acetate extract and chloroform methanol extract (T2) of Tripterygium wilfordii Hook. F Tao, X.;Cai, J.J.;Lipsky, P.E.
  28. Science v.274 Suppression of TNF-alpha-induced apoptosis by NF-kappaB Van Antwerp, O.J.;Martin, S.J.;Green, O.R.;Verma, I.M. https://doi.org/10.1126/science.274.5288.787
  29. Nat Med v.5 Tumoricidal activity of tumor necrosis factor-related apoptosisinducing ligand in vivo Walczak, H.;Miller, R.E.;Ariail, K.;Gliniak, B.;Griffith, T.S.;Kubin, M.;Chin, W.;Jones, J.;Woodward, A.;Le, T.;Smith, C.;Smolak, P.;Goodwin, R.G.;Rauch, C.T.;Schuh, J.C.;Lynch, O.H. https://doi.org/10.1038/5517
  30. Science v.274 TNF- and cancer therapy-induced apoptosis: potentiation by inhibition of NF-kappaB Wang, C.Y.;Mayo, M.W. Jr.;Baldwin, A.S. https://doi.org/10.1126/science.274.5288.784
  31. Science v.281 NF-kappaB antiapoptosis: induction of TRAF1 and TRAF2 and c-IAP1 and c-IAP2 to suppress caspase-8 activation Wang, C.Y.;Mayo, M.W.;Korneluk, R.G.;Goeddel, D.V. Jr.;Baldwin, A.S. https://doi.org/10.1126/science.281.5383.1680
  32. J Biol Chem v.273 Activation of nuclear factor-kappaB-dependent transcription by tumor necrosis factor-alpha is mediated through phosphorylation of RelNp65 on on serine 529 Wang, D. Jr.;Baldwin, A.S. https://doi.org/10.1074/jbc.273.45.29411
  33. J Biol Chem v.272 Cleavage of focal adhesion kinase by caspase during apoptosis Wen, L.P.;Fahrni, J.A.;Troie, S.;Guan, J.L.;Orth, K.;Rosen, G.D. https://doi.org/10.1074/jbc.272.41.26056
  34. Immunity v.3 Identification and characterization of a new mwmber of the TNF family that induces apoptosis Wiley, S.R.;Schooley, K.;Smolak, P.J.;Din, W.S.;Huang, C.P.;Nicholi, J.K.;Sutherland, G.R.;Smith, T.D.;Rauch, C.;Smith, C.A.;Goodwin, R.G. https://doi.org/10.1016/1074-7613(95)90057-8
  35. Mol. Cell v.1 Phosphorylation of NF-kappa B p65 by PKA stimulates transcriptional activity by promoting a novel bivalent interaction with the coactivator CBP/p300 Zhong, H.;Voll, R.E.;Ghosh, S. https://doi.org/10.1016/S1097-2765(00)80066-0