Re-use of established drugs for anti-metastatic indications Prof. Dr
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Re-use of established drugs for anti-metastatic indications Prof. Dr
Re-use of established drugs for anti-metastatic indications Prof. Dr. rer. nat. habil. Frank Entschladen - Chief Science Officer – MetaVì Labs Leukocytes: Immune response Stem cells: Tissue regeneration Cell Migration Tumor cells: Invasion and metastasis Fibroblasts: Wound healing Why is measuring cell migration in cancer so valuable? Invasion and Metastasis nervous system lymph nodes lymphogenic metastases distant metastases perineural invasion liver lung bone marrow T DC NG MΦ primary tumor hematogenic metastases Rationale and market need “It is local invasion and distant metastasis that kill rather than excessive cell proliferation per se.” Michael B. Sporn “The war on cancer.” 1996, Lancet over 90% of cancer deaths are due to metastasis there is currently no anti-metastatic drug available tumor cell migration is an essential prerequisite for invasion and metastasis “Until non-clinical models with good predictive properties have been defined… the absence of such models is considered to constitute the greatest hurdle for efficient drug development within the foreseeable future.” European Medicines Agency, Oncology Working Party “Guideline on the evaluation of anticancer medicinal products in man” 2011, EMA/CHMP/205/95/rev. 4 “A better understanding of the mechanisms of cell motility and cytoskeletal regulation may provide novel therapeutic strategies that would block metastatic progression, reducing dissemination of tumor cells and increasing patient survival.” Dmitriy Kedrin, Jacco van Rheenen, Lorena Hernandez, John Condeelis, Jeffrey E. Segall “Cell motility and cytoskeletal regulation in invasion and metastasis” 2007, J Mammary Gland Biol Neoplasia Growth Factors Extracellular Matrix Neurotransmi<ers Chemokines G Protein-‐Coupled Receptors (GPCRs) Cadherins α p120 α β γ GRK β-‐Catenin Receptor Tyrosine Kinases (RTKs) β-‐ArresFn srcPTK PLCγ PLB SERCA Calcium PKA Rap1 AF6 PI3K IP3+DAG cAMP EPAC PIP2 Vin PIP3 PIP2 Grb2 Ras Raf MEK1/2 ERK1/2 Sos PDK PKC AcFn Paxillin FAK AcFn GSK3β Integrins Talin Shc α-‐Catenin AC α Grb2 srcPTK ATP β EndoplasmaFc ReFculum KRIT AcFn Calcium GDI Tiam Vav2 Akt/PKB CaM/MLCK Calcium GEF MARCKS p130CAS PAK Cdc 42 ENA/ VASP Rho ROCK Rac Crk MLC PIP2 Non-‐muscle Myosin II AcFn AcFn WAVE WASP Calcium Gelsolin AcFn PIP2 Profilin Arp2/3 complex AcFn Schaap-Nutt et al. Curr. Pharm. Des., 2014 Beta-Blockers in vitro mouse model patient studies p=0.022 metastasis primary tumor p=0.013 Growth Factors Extracellular Matrix Neurotransmi<ers Chemokines G Protein-‐Coupled Receptors (GPCRs) Cadherins α p120 α β γ GRK β-‐Catenin Receptor Tyrosine Kinases (RTKs) β-‐ArresFn srcPTK PLCγ PLB SERCA Calcium PKA Rap1 AF6 PI3K IP3+DAG cAMP EPAC PIP2 Vin PIP3 PIP2 Grb2 Ras Raf MEK1/2 ERK1/2 Sos PDK PKC AcFn Paxillin FAK AcFn GSK3β Integrins Talin Shc α-‐Catenin AC α Grb2 srcPTK ATP β EndoplasmaFc ReFculum KRIT AcFn Calcium GDI Tiam Vav2 Akt/PKB CaM/MLCK Calcium GEF MARCKS p130CAS PAK Cdc 42 ENA/ VASP Rho ROCK Rac Crk MLC PIP2 Non-‐muscle Myosin II AcFn AcFn WAVE WASP Calcium Gelsolin AcFn PIP2 Profilin Arp2/3 complex AcFn Schaap-Nutt et al. Curr. Pharm. Des., 2014 Pharma-pipelines: Receptor Tyrosine Kinases Target EGFR EGFR/HER2 HER2 HER3 c-Met FGFR multi-RTK Substance name Company ABT-806 Abbott Panitumumab Amgen Erlotinib Astellas Gefitinib, Vandetanib AstraZeneca Cetuximab Bristol-Myers Squibb Nimotuzumab Daiichi-Sankyo Necitumumab Eli Lilly Matuzumab EMD Serono Erlotinib Merck Afatinib Boehringer Ingelheim Dacomitinib Pfizer TAK-165 Takeda Patritumab Daiichi-Sankyo LJM716 Novartis RG7116 Roche SAR256212 Sanofi-Aventis ABT-700 Abbott AMG208, AMG337 Amgen Tivantinib Daiichi-Sankyo LY2875358 Eli Lilly GSK1363089 GlaxoSmithKline JNJ38877605 Johnson&Johnson MK2461, MK8033 Merck AZD4547 AstraZeneca LY2874455 Eli Lilly BGJ398 Novartis ABT-348 Abbott Regorafenib Bayer Nintedanib Boehringer Ingelheim JNJ26483327 Johnson&Johnson Axitinib, Sunitinib Pfizer Schaap-Nutt et al. Curr. Pharm. Des., 2014 Regorafenib Growth Factors Extracellular Matrix Neurotransmi<ers Chemokines G Protein-‐Coupled Receptors (GPCRs) Cadherins α p120 α β γ GRK β-‐Catenin Receptor Tyrosine Kinases (RTKs) β-‐ArresFn srcPTK PLCγ PLB SERCA Calcium PKA Rap1 AF6 PI3K IP3+DAG cAMP EPAC PIP2 Vin PIP3 PIP2 Grb2 Ras Raf MEK1/2 ERK1/2 Sos PDK PKC AcFn Paxillin FAK AcFn GSK3β Integrins Talin Shc α-‐Catenin AC α Grb2 srcPTK ATP β EndoplasmaFc ReFculum KRIT AcFn Calcium GDI Tiam Vav2 Akt/PKB CaM/MLCK Calcium GEF MARCKS p130CAS PAK Cdc 42 ENA/ VASP Rho ROCK Rac Crk MLC PIP2 Non-‐muscle Myosin II AcFn AcFn WAVE WASP Calcium Gelsolin AcFn PIP2 Profilin Arp2/3 complex AcFn Schaap-Nutt et al. Curr. Pharm. Des., 2014 Pharma-pipelines: Signal Transduction Target Substance name GSK2141795, GSK2110183, Akt src FAK PI3K GSK690693 Company GlaxoSmithKline Target Substance name Company b-raf GSK2118436 GlaxoSmithKline pan-raf MLN2480 Takeda/Millenium MK-2206 Merck Refametinib Bayer RG7440 Roche BI847325 Boehringer Ingelheim Bosutinib Pfizer Primasertib EMD Serono GSK1120212 GlaxoSmithKline MEK BI853520 Boehringer Ingelheim GSK2256098 GlaxoSmithKline RG7167, RG7304, RG7420 Roche VS-6063, VS-4718 Verastem TAK-733 Takeda AMG319 Amgen Momelotinib Sciences SAR302503 Sanofi-Aventis MT103 Medisyn Technologies AEB071 Novartis BAY80-6946 Bayer DS-7423 Daiichi-Sankyo Idelalisib, GS-9820 Sciences GSK2636771, GSK2126458 GlaxoSmithKline BEZ235, Buparlisib, BYL719 Novartis PF-04691502, PF-05212348 Pfizer CHU Roche SAR245408, SAR245409 Sanofi-Aventis MLN1117 Takeda/Millenium VS-5584 Verastem JAK PKC Schaap-Nutt et al. Curr. Pharm. Des., 2014 Buparlisib (BKM120)
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