References
- 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
- Science v.281 Death receptors: signaling and modulation Ashkenazi, A.;Dixit, V.M. https://doi.org/10.1126/science.281.5381.1305
- 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
-
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 - 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.
- 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
- 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
- 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.
-
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. - 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.
- 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
- 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
-
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 - Cell v.88 p53, the cellular gatekeeper for growth and division Levine, A.J. https://doi.org/10.1016/S0092-8674(00)81871-1
- 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
- Cell v.88 Apoptosis by death factor Nagata, S. https://doi.org/10.1016/S0092-8674(00)81874-7
- 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
- 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
- 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
- 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
-
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 - 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.
- 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
- 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
- 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
- Cell v.76 The TNF-receptor superfamily of cellular and viral proteins: Activation, costimulation, and death Smith, C.A.;Farrah, T.;Goodwin, R.G.
- 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.
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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