Search Results - "Springer, Caroline J."

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    Kinase-Dead BRAF and Oncogenic RAS Cooperate to Drive Tumor Progression through CRAF by Heidorn, Sonja J., Milagre, Carla, Whittaker, Steven, Nourry, Arnaud, Niculescu-Duvas, Ion, Dhomen, Nathalie, Hussain, Jahan, Reis-Filho, Jorge S., Springer, Caroline J., Pritchard, Catrin, Marais, Richard

    Published in Cell (22-01-2010)
    “…We describe a mechanism of tumorigenesis mediated by kinase-dead BRAF in the presence of oncogenic RAS. We show that drugs that selectively inhibit BRAF drive…”
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    Mechanism of Activation of the RAF-ERK Signaling Pathway by Oncogenic Mutations of B-RAF by Wan, Paul T.C, Garnett, Mathew J, Roe, S.Mark, Lee, Sharlene, Niculescu-Duvaz, Dan, Good, Valerie M, Project, Cancer Genome, Jones, C.Michael, Marshall, Christopher J, Springer, Caroline J, Barford, David, Marais, Richard

    Published in Cell (19-03-2004)
    “…Over 30 mutations of the B-RAF gene associated with human cancers have been identified, the majority of which are located within the kinase domain. Here we…”
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    Synthesis of Novel Cationic Lipids:  Effect of Structural Modification on the Efficiency of Gene Transfer by Heyes, James A, Niculescu-Duvaz, Dan, Cooper, Robert G, Springer, Caroline J

    Published in Journal of medicinal chemistry (03-01-2002)
    “…A series of novel cationic lipids was designed and synthesized in an effort to understand the importance of the various structural features with respect to…”
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    BRAF as a therapeutic target: a patent review (2006 - 2012) by Zambon, Alfonso, Niculescu-Duvaz, Dan, Niculescu-Duvaz, Ion, Marais, Richard, Springer, Caroline J

    Published in Expert opinion on therapeutic patents (01-02-2013)
    “…After its identification as an oncogene in 2002, mutant BRAF has become the target of a number of drug discovery programmes, primarily aimed at the treatment…”
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    Small molecule inhibitors of BRAF in clinical trials by Zambon, Alfonso, Niculescu-Duvaz, Ion, Niculescu-Duvaz, Dan, Marais, Richard, Springer, Caroline J

    Published in Bioorganic & medicinal chemistry letters (15-01-2012)
    “…Over the last few years, BRAF has emerged as a validated target in melanoma. This review summarises recent advances in the development of BRAF inhibitors,…”
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    A Novel, Selective, and Efficacious Nanomolar Pyridopyrazinone Inhibitor of V600EBRAF by WHITTAKER, Steven, MENARD, Delphine, LAMBROS, Maryou, REIS-FILHO, Jorge S, MARAIS, Richard, SPRINGER, Caroline J, KIRK, Ruth, OGILVIE, Lesley, HEDLEY, Douglas, ZAMBON, Alfonso, LOPES, Filipa, PREECE, Natasha, MANNE, Helen, RANA, Sareena

    Published in Cancer research (Chicago, Ill.) (15-10-2010)
    “…Oncogenic BRAF is a critical driver of proliferation and survival and is thus a validated therapeutic target in cancer. We have developed a potent inhibitor,…”
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    Hyperpolarized 13C magnetic resonance detection of carboxypeptidase G2 activity by Jamin, Yann, Gabellieri, Cristina, Smyth, Lynette, Reynolds, Steven, Robinson, Simon P., Springer, Caroline J., Leach, Martin O., Payne, Geoffrey S., Eykyn, Thomas R.

    Published in Magnetic resonance in medicine (01-11-2009)
    “…Carboxypeptidase G2 (CPG2) is a bacterial enzyme that is currently employed in a range of targeted cancer chemotherapy strategies such as gene‐directed enzyme…”
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    Novel Fluorinated Prodrugs for Activation by Carboxypeptidase G2 Showing Good in Vivo Antitumor Activity in Gene-Directed Enzyme Prodrug Therapy by Davies, Lawrence C, Friedlos, Frank, Hedley, Douglas, Martin, Jan, Ogilvie, Lesley M, Scanlon, Ian J, Springer, Caroline J

    Published in Journal of medicinal chemistry (11-08-2005)
    “…Sixteen novel polyfluorinated benzoic acid mustards have been synthesized for use in gene-directed enzyme prodrug therapy (GDEPT). Eight of these were benzoic…”
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    B-RAF is a therapeutic target in melanoma by KARASARIDES, Maria, CHILOECHES, Antonio, SPRINGER, Caroline J, MARAIS, Richard, HAYWARD, Robert, NICULESCU-DUVAZ, Dan, SCANLON, Ian, FRIEDLOS, Frank, OGILVIE, Lesley, HEDLEY, Douglas, MARTIN, Jan, MARSHALL, Christopher J

    Published in Oncogene (19-08-2004)
    “…B-RAF is a serine/threonine-specific protein kinase that is mutated in approximately 70% of human melanomas. However, the role of this signalling molecule in…”
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    Potent BRAF kinase inhibitors based on 2,4,5-trisubstituted imidazole with naphthyl and benzothiophene 4-substituents by Niculescu-Duvaz, Dan, Niculescu-Duvaz, Ion, Suijkerbuijk, Bart M.J.M., Ménard, Delphine, Zambon, Alfonso, Davies, Lawrence, Pons, Jean-Francois, Whittaker, Steven, Marais, Richard, Springer, Caroline J.

    Published in Bioorganic & medicinal chemistry (01-03-2013)
    “…The RAS–RAF–MEK–ERK pathway is hyperactivated in 30% of human cancers. BRAF is a serine–threonine kinase, belonging to this pathway that is mutated with high…”
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    Suicide gene therapy of human colon carcinoma xenografts using an armed oncolytic adenovirus expressing carboxypeptidase G2 by SCHEPELMANN, Silke, OGILVIE, Lesley M, HEDLEY, Douglas, FRIEDLOS, Frank, MARTIN, Janet, SCANLON, Ian, PING CHEN, MARAIS, Richard, SPRINGER, Caroline J

    Published in Cancer research (Chicago, Ill.) (15-05-2007)
    “…We have designed a targeted systemic suicide gene therapy that combines the advantages of tumor-selective gene expression, using the human telomerase promoter…”
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    Detection of the Prodrug-Activating Enzyme Carboxypeptidase G2 Activity with Chemical Exchange Saturation Transfer Magnetic Resonance by Jamin, Yann, Eykyn, Thomas R., Poon, Evon, Springer, Caroline J., Robinson, Simon P.

    Published in Molecular imaging and biology (01-04-2014)
    “…Purpose The purpose of this study is to evaluate if the differential exchange rates with bulk water between amine and amide protons can be exploited using…”
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    Selective activation of anticancer prodrugs by monoclonal antibody–enzyme conjugates by Senter, Peter D, Springer, Caroline J

    Published in Advanced drug delivery reviews (31-12-2001)
    “…A great deal of interest has surrounded the activities of monoclonal antibodies (mAbs), and mAb–drug, toxin and radionuclide conjugates for the treatment of…”
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    Long Functionalized Poly(ethylene glycol)s of Defined Molecular Weight: Synthesis and Application in Solid-Phase Synthesis of Conjugates by Niculescu-Duvaz, Dan, Getaz, Jayne, Springer, Caroline J

    Published in Bioconjugate chemistry (01-04-2008)
    “…A concise synthesis of long-chain poly(ethylene glycol) (PEG) of defined molecular weight up to 29 ethyleneoxy units is described. These PEG diols were…”
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