Search Results - "Dredge, K."
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The evolution of thalidomide and its IMiD derivatives as anticancer agents
Published in Nature reviews. Cancer (01-04-2004)“…Thalidomide was originally used to treat morning sickness, but was banned in the 1960s for causing serious congenital birth defects. Remarkably, thalidomide…”
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PG545, a dual heparanase and angiogenesis inhibitor, induces potent anti-tumour and anti-metastatic efficacy in preclinical models
Published in British journal of cancer (15-02-2011)“…Background: PG545 is a heparan sulfate (HS) mimetic that inhibits tumour angiogenesis by sequestering angiogenic growth factors in the extracellular matrix…”
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The PG500 series: novel heparan sulfate mimetics as potent angiogenesis and heparanase inhibitors for cancer therapy
Published in Investigational new drugs (01-06-2010)“…Summary Heparan sulfate mimetics, which we have called the PG500 series, have been developed to target the inhibition of both angiogenesis and heparanase…”
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Novel thalidomide analogues display anti-angiogenic activity independently of immunomodulatory effects
Published in British journal of cancer (04-11-2002)“…The anti-tumour effects of thalidomide have been associated with its anti-angiogenic properties. Second generation thalidomide analogues are distinct compounds…”
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Phase I study to determine the safety, tolerability and immunostimulatory activity of thalidomide analogue CC-5013 in patients with metastatic malignant melanoma and other advanced cancers
Published in British journal of cancer (08-03-2004)“…We assessed the safety, tolerability and efficacy of the immunomodulatory drug, CC-5013 (REVIMID trade mark ), in the treatment of patients with metastatic…”
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Thalidomide and its analogues have distinct and opposing effects on TNF‐α and TNFR2 during co‐stimulation of both CD4+ and CD8+ T cells
Published in Clinical and experimental immunology (01-10-2002)“…Summary Thalidomide (Thd) is clinically useful in a number of conditions where its efficacy is probably related to its anti‐TNF‐α activity. More recently, Thd…”
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Protective Antitumor Immunity Induced by a Costimulatory Thalidomide Analog in Conjunction with Whole Tumor Cell Vaccination Is Mediated by Increased Th1-Type Immunity
Published in The Journal of immunology (1950) (15-05-2002)“…Thalidomide and its novel T cell costimulatory analogs (immunomodulatory drugs) are currently being assessed in the treatment of patients with advanced cancer…”
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polyamine analog PG11047 potentiates the antitumor activity of cisplatin and bevacizumab in preclinical models of lung and prostate cancer
Published in Cancer chemotherapy and pharmacology (01-12-2009)“…Purpose PG11047 is a polyamine analog currently in Phase I trials for advanced cancer as a monotherapy and in combination with a number of approved anti-cancer…”
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Adjuvants and the promotion of Th1-type cytokines in tumour immunotherapy
Published in Cancer Immunology, Immunotherapy (01-11-2002)“…Immunotherapy includes both active and passive mechanisms that have the potential to treat many tumour types. Whereas monoclonal antibodies may kill cells by…”
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Orally administered lenalidomide (CC-5013) is anti-angiogenic in vivo and inhibits endothelial cell migration and Akt phosphorylation in vitro
Published in Microvascular research (2005)“…The thalidomide analogue and immunomodulatory drug (IMiD®) lenalidomide (CC-5013, REVLIMID™) is emerging as a useful treatment for a number of cancers and has…”
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Vitamin D receptor‐dependent antitumour effects of 1,25‐dihydroxyvitamin D 3 and two synthetic analogues in three in vivo models of prostate cancer
Published in BJU international (01-10-2002)“…Objective To determine the in vitro and in vivo effects of 1,25‐dihydroxyvitamin D 3 (calcitriol) and two newer less hypercalcaemic analogues, EB1089 and…”
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Vitamin D receptor‐dependent antitumour effects of 1,25‐dihydroxyvitamin D3 and two synthetic analogues in three in vivo models of prostate cancer
Published in BJU international (01-10-2002)“…Objective To determine the in vitro and in vivo effects of 1,25‐dihydroxyvitamin D 3 (calcitriol) and two newer less hypercalcaemic analogues, EB1089 and…”
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A novel subclass of thalidomide analogue with anti-solid tumor activity in which caspase-dependent apoptosis is associated with altered expression of bcl-2 family proteins
Published in Cancer research (Chicago, Ill.) (01-02-2003)“…Thalidomide is clinically useful in a number of cancers. Antitumor activity may be related to a number of known properties, including anti-tumor necrosis…”
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Thalidomide analogs as emerging anti-cancer drugs
Published in Anti-cancer drugs (01-06-2003)“…Recently, it has been demonstrated that a number of novel thalidomide analogs possess anti-cancer properties due to their T cell co-stimulatory,…”
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Activity and onset of action of reboxetine and effect of combination with sertraline in an animal model of depression
Published in European journal of pharmacology (08-01-1999)“…The limitations of antidepressant drugs to treat depression has warranted ongoing research to identify pharmacological agents and strategies which offer a…”
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Immunological effects of thalidomide and its chemical and functional analogs
Published in Critical reviews in immunology (2002)“…Thalidomide has recently shown considerable promise in the treatment of a number of conditions, such as leprosy and cancer. Its effectiveness in the clinic has…”
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Novel Vibrio cholerae O139 genes involved in lipopolysaccharide biosynthesis
Published in Journal of Bacteriology (01-04-1997)“…Article Usage Stats Services JB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Efficacy of intramammary treatment with procaine penicillin G vs. procaine penicillin G plus neomycin in bovine clinical mastitis caused by penicillin-susceptible, gram-positive bacteria - a double blind field study
Published in Journal of veterinary pharmacology and therapeutics (01-06-2003)“…The efficacy of intramammary treatments containing procaine penicillin G alone (treatment A) or a combination of procaine penicillin G and neomycin (treatment…”
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