Search Results - "Springer, Caroline J."
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1
Kinase-Dead BRAF and Oncogenic RAS Cooperate to Drive Tumor Progression through CRAF
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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2
Mechanism of Activation of the RAF-ERK Signaling Pathway by Oncogenic Mutations of B-RAF
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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3
Primary melanoma of the CNS in children is driven by congenital expression of oncogenic NRAS in melanocytes
Published in Cancer discovery (01-04-2013)“…NRAS mutations are common in human melanoma. To produce a mouse model of NRAS-driven melanoma, we expressed oncogenic NRAS (NRAS(G12D)) in mouse melanocytes…”
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4
Attenuated Salmonella Targets Prodrug Activating Enzyme Carboxypeptidase G2 to Mouse Melanoma and Human Breast and Colon Carcinomas for Effective Suicide Gene Therapy
Published in Clinical cancer research (01-07-2008)“…Purpose: We engineered the oncolytic Salmonella typhimurium –derived bacterium VNP20009 as a vector to target delivery to tumors of the prodrug-activating…”
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5
Synthesis of Novel Cationic Lipids: Effect of Structural Modification on the Efficiency of Gene Transfer
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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6
A Phase I Study of Single Administration of Antibody-Directed Enzyme Prodrug Therapy with the Recombinant Anti–Carcinoembryonic Antigen Antibody-Enzyme Fusion Protein MFECP1 and a Bis-Iodo Phenol Mustard Prodrug
Published in Clinical cancer research (01-11-2006)“…Purpose: Antibody-directed enzyme prodrug therapy is a two-stage treatment whereby a tumor-targeted antibody-enzyme complex localizes in tumor for selective…”
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7
BRAF as a therapeutic target: a patent review (2006 - 2012)
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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8
Investigating the Contribution of Collagen to the Tumor Biomechanical Phenotype with Noninvasive Magnetic Resonance Elastography
Published in Cancer research (Chicago, Ill.) (15-11-2019)“…Increased stiffness in the extracellular matrix (ECM) contributes to tumor progression and metastasis. Therefore, stromal modulating therapies and accompanying…”
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9
Small molecule inhibitors of BRAF in clinical trials
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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10
A Novel, Selective, and Efficacious Nanomolar Pyridopyrazinone Inhibitor of V600EBRAF
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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11
Hyperpolarized 13C magnetic resonance detection of carboxypeptidase G2 activity
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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12
Preclinical Evidence That Trametinib Enhances the Response to Antiangiogenic Tyrosine Kinase Inhibitors in Renal Cell Carcinoma
Published in Molecular cancer therapeutics (01-01-2016)“…Sunitinib and pazopanib are antiangiogenic tyrosine kinase inhibitors (TKI) used to treat metastatic renal cell carcinoma (RCC). However, the ability of these…”
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13
Novel Fluorinated Prodrugs for Activation by Carboxypeptidase G2 Showing Good in Vivo Antitumor Activity in Gene-Directed Enzyme Prodrug Therapy
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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14
B-RAF is a therapeutic target in melanoma
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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15
Contrasting effects of sunitinib within in vivo models of metastasis
Published in Angiogenesis (London) (01-12-2012)“…Sunitinib is a potent and clinically approved tyrosine kinase inhibitor that can suppress tumour growth by inhibiting angiogenesis. However, conflicting data…”
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Potent BRAF kinase inhibitors based on 2,4,5-trisubstituted imidazole with naphthyl and benzothiophene 4-substituents
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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17
Suicide gene therapy of human colon carcinoma xenografts using an armed oncolytic adenovirus expressing carboxypeptidase G2
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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18
Detection of the Prodrug-Activating Enzyme Carboxypeptidase G2 Activity with Chemical Exchange Saturation Transfer Magnetic Resonance
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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19
Selective activation of anticancer prodrugs by monoclonal antibody–enzyme conjugates
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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20
Long Functionalized Poly(ethylene glycol)s of Defined Molecular Weight: Synthesis and Application in Solid-Phase Synthesis of Conjugates
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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