Anticancer therapy targeting the apoptotic pathway.
暂无分享,去创建一个
[1] G. Evan,et al. Nuclear colocalization of cellular and viral myc proteins with HSP70 in myc-overexpressing cells , 1991, Journal of virology.
[2] P. Hainaut,et al. Interaction of heat‐shock protein 70 with p53 translated in vitro: evidence for interaction with dimeric p53 and for a role in the regulation of p53 conformation. , 1992, The EMBO journal.
[3] B. Cheson,et al. Clinical trials referral resource. , 1990, Oncology.
[4] John Calvin Reed,et al. Tumor suppressor p53 is a direct transcriptional activator of the human bax gene , 1995, Cell.
[5] H. Villar,et al. Design, synthesis, and evaluation of latent alkylating agents activated by glutathione S-transferase. , 1996, Journal of medicinal chemistry.
[6] John Calvin Reed,et al. BCL‐2 family proteins: Regulators of cell death involved in the pathogenesis of cancer and resistance to therapy , 1996, Journal of cellular biochemistry.
[7] R. Meadows,et al. Structure of Bcl-xL-Bak Peptide Complex: Recognition Between Regulators of Apoptosis , 1997, Science.
[8] R. James,et al. Induction of caspase-3 protease activity and apoptosis by butyrate and trichostatin A (inhibitors of histone deacetylase): dependence on protein synthesis and synergy with a mitochondrial/cytochrome c-dependent pathway. , 1997, Cancer research.
[9] D. Green,et al. The Release of Cytochrome c from Mitochondria: A Primary Site for Bcl-2 Regulation of Apoptosis , 1997, Science.
[10] D. V. Von Hoff,et al. Activity of TER286 against human tumor colony-forming units. , 1997, Anti-cancer drugs.
[11] D. Altieri,et al. A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma , 1997, Nature Medicine.
[12] John Calvin Reed,et al. BAG‐1 modulates the chaperone activity of Hsp70/Hsc70 , 1997, The EMBO journal.
[13] John Calvin Reed,et al. The c‐IAP‐1 and c‐IAP‐2 proteins are direct inhibitors of specific caspases , 1997, The EMBO journal.
[14] S. Srinivasula,et al. Cytochrome c and dATP-Dependent Formation of Apaf-1/Caspase-9 Complex Initiates an Apoptotic Protease Cascade , 1997, Cell.
[15] Fengzhi Li,et al. Control of apoptosis and mitotic spindle checkpoint by survivin , 1998, Nature.
[16] S. Lippman,et al. Adenovirus-mediated p53 gene transfer in patients with advanced recurrent head and neck squamous cell carcinoma. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[17] S. Cory,et al. The Bcl-2 protein family: arbiters of cell survival. , 1998, Science.
[18] P. Marks,et al. A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[19] J C Reed,et al. IAPs block apoptotic events induced by caspase‐8 and cytochrome c by direct inhibition of distinct caspases , 1998, The EMBO journal.
[20] J C Reed,et al. Cleavage of human inhibitor of apoptosis protein XIAP results in fragments with distinct specificities for caspases , 1999, The EMBO journal.
[21] G. Clayman,et al. Local delivery for gene therapy , 1999, Current oncology reports.
[22] Andreeff,et al. Apoptosis regulating proteins as targets of therapy for haematological malignancies. , 1999, Expert opinion on investigational drugs.
[23] R. K Srivastava,et al. Deletion of the loop region of Bcl-2 completely blocks paclitaxel-induced apoptosis. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[24] C. Rauch,et al. Tumoricidal activity of tumor necrosis factor–related apoptosis–inducing ligand in vivo , 1999, Nature Medicine.
[25] M MacFarlane,et al. Distinct Caspase Cascades Are Initiated in Receptor-mediated and Chemical-induced Apoptosis* , 1999, The Journal of Biological Chemistry.
[26] E. Sausville,et al. Proteasome inhibitors: a novel class of potent and effective antitumor agents. , 1999, Cancer research.
[27] S. Korsmeyer,et al. BCL-2 family members and the mitochondria in apoptosis. , 1999, Genes & development.
[28] B. Cheson,et al. Clinical trials referral resource. Current clinical trials for the proteasome inhibitor PS-341. , 2000, Oncology.
[29] Yi Li Yang,et al. The IAP family: endogenous caspase inhibitors with multiple biological activities , 2000, Cell Research.
[30] M. Hengartner. The biochemistry of apoptosis , 2000, Nature.
[31] R. Morimoto,et al. The Chaperone Function of hsp70 Is Required for Protection against Stress-Induced Apoptosis , 2000, Molecular and Cellular Biology.
[32] S. Korsmeyer,et al. Pro-apoptotic cascade activates BID, which oligomerizes BAK or BAX into pores that result in the release of cytochrome c , 2000, Cell Death and Differentiation.
[33] D. Cunningham,et al. Phase I clinical and pharmacokinetic study of bcl-2 antisense oligonucleotide therapy in patients with non-Hodgkin's lymphoma. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[34] T. Cotter,et al. Heat shock proteins – modulators of apoptosis in tumour cells , 2000, Leukemia.
[35] Dick D. Mosser,et al. Heat-shock protein 70 inhibits apoptosis by preventing recruitment of procaspase-9 to the Apaf-1 apoptosome , 2000, Nature Cell Biology.
[36] H. Inagawa,et al. A new method of antitumor therapy with a high dose of TNF perfusion for unresectable liver tumors. , 2000, Anticancer research.
[37] K. Tew,et al. Cellular response to a glutathione S-transferase P1-1 activated prodrug. , 2000, Molecular pharmacology.
[38] Emad S. Alnemri,et al. Negative regulation of the Apaf-1 apoptosome by Hsp70 , 2000, Nature Cell Biology.
[39] R. Davis,et al. Signal Transduction by the JNK Group of MAP Kinases , 2000, Cell.
[40] P. Binz,et al. Heat shock proteins in human cancer , 2000, Electrophoresis.
[41] S. Strom,et al. Apoptosis induced in normal human hepatocytes by tumor necrosis factor-related apoptosis-inducing ligand , 2000, Nature Medicine.
[42] H. Kalthoff,et al. CD95 and TRAIL receptor-mediated activation of protein kinase C and NF-κB contributes to apoptosis resistance in ductal pancreatic adenocarcinoma cells , 2001, Oncogene.
[43] I. Brukner. INGN-201. Introgen Therapeutics. , 2001, Current opinion in investigational drugs.
[44] Josef M. Penninger,et al. Heat-shock protein 70 antagonizes apoptosis-inducing factor , 2001, Nature Cell Biology.
[45] P. Elliott,et al. The proteasome: a new target for novel drug therapies. , 2001, American journal of clinical pathology.
[46] M. Gleave,et al. Synergistic chemosensitization and inhibition of progression to androgen independence by antisense Bcl‐2 oligodeoxynucleotide and paclitaxel in the LNCaP prostate tumor model , 2001, International journal of cancer.
[47] T. Owa,et al. Cell cycle regulation in the G1 phase: a promising target for the development of new chemotherapeutic anticancer agents. , 2001, Current medicinal chemistry.
[48] P. Richardson,et al. TRAIL/Apo2L ligand selectively induces apoptosis and overcomes drug resistance in multiple myeloma: therapeutic applications. , 2001, Blood.
[49] J. Adams,et al. Proteasome inhibition in cancer: development of PS-341. , 2001, Seminars in oncology.
[50] S. Korsmeyer,et al. Proapoptotic BAX and BAK: A Requisite Gateway to Mitochondrial Dysfunction and Death , 2001, Science.
[51] N. Tanigawa,et al. The role of survivin as a new target of diagnosis and treatment in human cancer , 2001, Medical Electron Microscopy.
[52] Xianglin Shi,et al. New Insights into the Role of Nuclear Factor-κB in Cell Growth Regulation , 2001 .
[53] L. Corcos,et al. Anticancer agents sensitize tumor cells to tumor necrosis factor-related apoptosis-inducing ligand-mediated caspase-8 activation and apoptosis. , 2001, Cancer research.
[54] P. Workman,et al. Inhibition of signal transduction by the Hsp90 inhibitor 17-allylamino-17-demethoxygeldanamycin results in cytostasis and apoptosis. , 2001, Cancer research.
[55] L. Neckers,et al. Measurement of the novel antitumor agent 17-(allylamino)-17-demethoxygeldanamycin in human plasma by high-performance liquid chromatography. , 2001, Journal of chromatography. B, Biomedical sciences and applications.
[56] P. Marks,et al. Histone deacetylases and cancer: causes and therapies , 2001, Nature Reviews Cancer.
[57] R. K Srivastava. TRAIL/Apo-2L: mechanisms and clinical applications in cancer. , 2001, Neoplasia.
[58] S. Park,et al. Alternative splicing variants of c-FLIP transduce the differential signal through the Raf or TRAF2 in TNF-induced cell proliferation. , 2001, Biochemical and biophysical research communications.
[59] J. Blank,et al. The ups and downs of MEK kinase interactions. , 2001, Cellular signalling.
[60] A. Tolcher. Preliminary phase I results of G3139 (bcl-2 antisense oligonucleotide) therapy in combination with docetaxel in hormone-refractory prostate cancer. , 2001, Seminars in oncology.
[61] C. Rudin,et al. ONYX-015. Onyx Pharmaceuticals. , 2001, Current opinion in investigational drugs.
[62] T. Libermann,et al. Molecular sequelae of proteasome inhibition in human multiple myeloma cells , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[63] C. Rudin,et al. A pilot trial of G3139, a bcl-2 antisense oligonucleotide, and paclitaxel in patients with chemorefractory small-cell lung cancer. , 2002, Annals of oncology : official journal of the European Society for Medical Oncology.
[64] John Calvin Reed,et al. Apoptosis-based therapies , 2002, Nature Reviews Drug Discovery.
[65] Michael Fraser,et al. Role of X-linked inhibitor of apoptosis protein in chemoresistance in ovarian cancer: possible involvement of the phosphoinositide-3 kinase/Akt pathway. , 2002, Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy.
[66] J. Hiscott,et al. On the TRAIL to apoptosis. , 2002, Cytokine & growth factor reviews.
[67] G. l'Allemain. [Update on . . . the proteasome inhibitor PS341]. , 2002, Bulletin du cancer.
[68] G. L’Allemain. Actualités sur... l'inhibiteur du protéasome PS341 , 2002 .
[69] B. Barlogie,et al. High-dose therapy and immunomodulatory drugs in multiple myeloma. , 2002, Seminars in oncology.
[70] K. Totpal,et al. Enhanced tumor killing by Apo2L/TRAIL and CPT-11 co-treatment is associated with p21 cleavage and differential regulation of Apo2L/TRAIL ligand and its receptors , 2002, Oncogene.
[71] B. Sela,et al. [Survivin: anti-apoptosis protein and a prognostic marker for tumor progression and recurrence]. , 2002, Harefuah.
[72] J. Licht,et al. Histone deacetylases as therapeutic targets in hematologic malignancies. , 2002, Current opinion in hematology.
[73] Karen L. Siedlecki,et al. Phase I trial of BCL-2 antisense oligonucleotide (G3139) administered by continuous intravenous infusion in patients with advanced cancer. , 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.
[74] S. Lipton,et al. Dueling Activities of AIF in Cell Death versus Survival DNA Binding and Redox Activity , 2002, Cell.
[75] J. Adams. Proteasome inhibition: a novel approach to cancer therapy. , 2002, Trends in molecular medicine.
[76] K. Tanabe,et al. Current status of the molecular mechanisms of anticancer drug-induced apoptosis , 2002, Cancer Chemotherapy and Pharmacology.
[77] R. Moritz,et al. HtrA2 Promotes Cell Death through Its Serine Protease Activity and Its Ability to Antagonize Inhibitor of Apoptosis Proteins* , 2002, The Journal of Biological Chemistry.
[78] G. Tortora,et al. Inhibition of bcl-2 as cancer therapy. , 2002, Annals of oncology : official journal of the European Society for Medical Oncology.
[79] J. Adams. Development of the proteasome inhibitor PS-341. , 2002, The oncologist.
[80] D. Neuberg,et al. Proteasome inhibitor PS-341 inhibits human myeloma cell growth in vivo and prolongs survival in a murine model. , 2002, Cancer research.
[81] M. Jäättelä. Programmed cell death: many ways for cells to die decently , 2002, Annals of medicine.
[82] E. White,et al. Regulation of the mitochondrial checkpoint in p53-mediated apoptosis confers resistance to cell death , 2002, Oncogene.
[83] G. Wood,et al. Apoptosis and melanoma: molecular mechanisms , 2003, The Journal of pathology.
[84] L. Mao,et al. Proteomic identification of heat shock protein 70 as a candidate target for enhancing apoptosis induced by farnesyl transferase inhibitor , 2003, Proteomics.
[85] C. Stroh,et al. Anticancer drugs of tomorrow: apoptotic pathways as targets for drug design. , 2003, Drug discovery today.
[86] L. Kèlland,et al. Farnesyl transferase inhibitors in the treatment of breast cancer , 2003, Expert opinion on investigational drugs.
[87] L. Neckers. Development of small molecule Hsp90 inhibitors: utilizing both forward and reverse chemical genomics for drug identification. , 2003, Current medicinal chemistry.
[88] N. Smith,et al. The p53 tumor suppressor gene and nuclear protein: basic science review and relevance in the management of bladder cancer. , 2003, The Journal of urology.
[89] R. Maestro,et al. Role of Caspases, Bid, and p53 in the Apoptotic Response Triggered by Histone Deacetylase Inhibitors Trichostatin-A (TSA) and Suberoylanilide Hydroxamic Acid (SAHA)* , 2003, The Journal of Biological Chemistry.
[90] X. Liu,et al. Survivin Enhances Aurora-B Kinase Activity and Localizes Aurora-B in Human Cells* , 2003, The Journal of Biological Chemistry.
[91] M. Peter,et al. The CD95(APO-1/Fas) DISC and beyond , 2003, Cell Death and Differentiation.
[92] L. Khachigian,et al. Signaling and transcriptional control of Fas ligand gene expression , 2003, Cell Death and Differentiation.
[93] A. Ashkenazi,et al. Apo2L/TRAIL and its death and decoy receptors , 2003, Cell Death and Differentiation.
[94] E. D. de Vries,et al. Death Receptor Ligands, in Particular TRAIL, to Overcome Drug Resistance , 2004, Cancer and Metastasis Reviews.
[95] L. Neckers,et al. Geldanamycin as a Potential Anti-Cancer Agent: Its Molecular Target and Biochemical Activity , 2004, Investigational New Drugs.
[96] M. Grever,et al. Preclinical pharmacologic evaluation of geldanamycin as an antitumor agent , 2004, Cancer Chemotherapy and Pharmacology.
[97] R. Korneluk,et al. XIAP: Apoptotic brake and promising therapeutic target , 2001, Apoptosis.
[98] P. Elliott,et al. Proteasome Inhibition: a New Strategy in Cancer Treatment , 2000, Investigational New Drugs.