Search Results - "Joel, Simon P."
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The Association of CCND1 Overexpression and Cisplatin Resistance in Testicular Germ Cell Tumors and Other Cancers
Published in The American journal of pathology (01-06-2010)“…Development of chemoresistance limits the clinical efficiency of platinum-based therapy. Although many resistance mechanisms have been demonstrated,…”
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The proteasome inhibitor bortezomib acts independently of p53 and induces cell death via apoptosis and mitotic catastrophe in B-cell lymphoma cell lines
Published in Cancer research (Chicago, Ill.) (15-03-2007)“…Bortezomib is a proteasome inhibitor with proven efficacy in multiple myeloma and non-Hodgkin's lymphoma. This study reports the effects of bortezomib in…”
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Bortezomib Therapy in Patients With Relapsed or Refractory Lymphoma: Potential Correlation of In Vitro Sensitivity and Tumor Necrosis Factor Alpha Response With Clinical Activity
Published in Journal of clinical oncology (01-05-2006)“…To determine the efficacy of bortezomib in patients with lymphoid malignancy, correlating clinical response with effect on plasma cytokines and in vitro…”
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Raman spectroscopic analysis of breast cancer tissues: identifying differences between normal, invasive ductal carcinoma and ductal carcinoma in situ of the breast tissue
Published in Journal of Raman spectroscopy (01-10-2007)“…A relatively non‐destructive method employing Raman spectroscopy for the analysis of histopathological specimens is described. Raman spectroscopy has allowed…”
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Capabilities of HPLC with APEX-Q nebulisation ICP-MS and ESI MS/MS to compare selenium uptake and speciation of non-malignant with different B cell lymphoma lines
Published in Analytical and bioanalytical chemistry (01-02-2011)“…The formation of intracellular dimethylselenide (DMSe) as a product of exposure of non-malignant (PBMCs) and lymphoma (RL and DHL-4) cell lines to…”
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Repression of sphingosine kinase (SK)-interacting protein (SKIP) in acute myeloid leukemia diminishes SK activity and its re-expression restores SK function
Published in The Journal of biological chemistry (17-04-2020)“…Previous studies have shown that sphingosine kinase interacting protein (SKIP) inhibits sphingosine kinase (SK) function in fibroblasts. SK phosphorylates…”
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DNA damage is able to induce senescence in tumor cells in vitro and in vivo
Published in Cancer research (Chicago, Ill.) (15-03-2002)“…Often the use of cytotoxic drugs in cancer therapy results in stable disease rather than regression of the tumor, and this is typically seen as a failure of…”
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Phase I and Pharmacokinetic Study of Intravenous Irinotecan Plus Oral Ciclosporin in Patients With Fluorouracil-Refractory Metastatic Colon Cancer
Published in Journal of clinical oncology (15-03-2003)“…Purpose: To assess the safety and toxicity profile of escalating doses of intravenous irinotecan, in combination with a fixed dose of oral ciclosporin (Cs) and…”
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Methylseleninic acid inhibits HDAC activity in diffuse large B-cell lymphoma cell lines
Published in Cancer chemotherapy and pharmacology (01-09-2011)“…Purpose Selenium is a trace element that is fundamental to human health. Research has mainly focussed on its role in cancer prevention, but recent evidence…”
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Lesional-targeting of neuroprotection to the inflammatory penumbra in experimental multiple sclerosis
Published in Brain (London, England : 1878) (2014)“…Progressive multiple sclerosis is associated with metabolic failure of the axon and excitotoxicity that leads to chronic neurodegeneration. Global…”
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Chemosensitization of B-Cell Lymphomas by Methylseleninic Acid Involves Nuclear Factor-κB Inhibition and the Rapid Generation of Other Selenium Species
Published in Cancer research (Chicago, Ill.) (15-11-2007)“…Abstract Although recent reports suggest that selenium can modulate the activity of cytotoxic drugs, the mechanism underlying this activity remains unclear…”
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The histone deacetylase inhibitor UCL67022 has potent activity in multiple myeloma and non‐Hodgkin lymphoma pre‐clinical models
Published in British journal of haematology (01-10-2013)Get full text
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Morphine analgesia in cancer pain: role of the glucuronides
Published in Journal of opioid management (01-05-2005)“…Preclinical data and limited studies in humans have suggested that morphine-6-glucuronide (M6G) has analgesic activity and morphine-3-glucuronide (M3G),…”
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The bioavailability of morphine applied topically to cutaneous ulcers
Published in Journal of pain and symptom management (01-05-2004)“…A number of studies have reported the analgesic effect of morphine when applied topically to painful skin ulcers. It has been suggested that morphine may exert…”
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Identification of genomic changes associated with cisplatin resistance in testicular germ cell tumor cell lines
Published in Genes chromosomes & cancer (01-07-2008)“…Since the introduction of cisplatin into the clinic, the treatment of patients with a variety of solid tumors including testicular germ cell tumors, ovarian…”
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Randomized placebo-controlled trial of the activity of the morphine glucuronides
Published in Clinical pharmacology and therapeutics (01-12-2000)“…Background Morphine‐6‐glucuronide (M6G) is an active metabolite of morphine with potent analgesic activity. Morphine‐3‐glucuronide (M3G), the most prevalent…”
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Aromatic Sulfide Inhibitors of Histone Deacetylase Based on Arylsulfinyl-2,4-hexadienoic Acid Hydroxyamides
Published in Journal of medicinal chemistry (26-01-2006)“…The synthesis of a novel series of potent inhibitors of histone deacetylases is described, based on arylsulfinyl-2,4-hexadienoic acid hydroxyamides and their…”
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Structure–activity relationships of aryloxyalkanoic acid hydroxyamides as potent inhibitors of histone deacetylase
Published in Bioorganic & medicinal chemistry letters (2007)“…Aryl ether inhibitors of histone deacetylase are described. Syntheses of aryloxyalkanoic acid hydroxyamides are described, all of which are potent inhibitors…”
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The bioavailability and pharmacokinetics of subcutaneous, nebulized and oral morphine‐6‐glucuronide
Published in British journal of clinical pharmacology (01-04-2002)“…Aims Morphine‐6‐glucuronide (M6G), one of the active metabolites of morphine, has attracted considerable interest as a potent opioid analgesic with an…”
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