Search Results - "Worland, Peter J."
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Pomalidomide and Lenalidomide Induce p21WAF-1 Expression in Both Lymphoma and Multiple Myeloma through a LSD1-Mediated Epigenetic Mechanism
Published in Cancer research (Chicago, Ill.) (15-09-2009)“…Lenalidomide and pomalidomide have both been evaluated clinically for their properties as anticancer agents, with lenalidomide being available commercially. We…”
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A prostate-specific membrane antigen-targeted monoclonal antibody-chemotherapeutic conjugate designed for the treatment of prostate cancer
Published in Cancer research (Chicago, Ill.) (01-11-2004)“…MLN2704 is an antibody-chemotherapeutic conjugate designed to target prostate-specific membrane antigen (PSMA). PSMA is a transmembrane receptor whose…”
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Flavopiridol induces G1 arrest with inhibition of cyclin-dependent kinase (CDK) 2 and CDK4 in human breast carcinoma cells
Published in Cancer research (Chicago, Ill.) (01-07-1996)“…Flavopiridol (L86-8275), a N-methylpiperidinyl, chlorophenyl flavone, can inhibit cell cycle progression in either G1 or G2 and is a potent cyclin-dependent…”
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Down-regulation of cyclin D1 by transcriptional repression in MCF-7 human breast carcinoma cells induced by flavopiridol
Published in Cancer research (Chicago, Ill.) (15-09-1999)“…Flavopiridol is a novel flavonoid that induces cell cycle arrest at different stages of the cell cycle because of the inhibition of cyclin-dependent kinases…”
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UCN-01: a Potent Abrogator of G2 Checkpoint Function in Cancer Cells With Disrupted p53
Published in JNCI : Journal of the National Cancer Institute (17-07-1996)“…Background: Arrest of the cell cycle in G2 phase following DNA damage helps protect cell viability by allowing time for DNA repair before entry into mitosis (M…”
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Anticancer antibodies
Published in American journal of clinical pathology (01-04-2003)“…The recent clinical and commercial success of anticancer antibodies such as rituximab and trastuzumab has created great interest in antibody-based therapeutics…”
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Structural Basis for Specificity and Potency of a Flavonoid Inhibitor of Human CDK2, a Cell Cycle Kinase
Published in Proceedings of the National Academy of Sciences - PNAS (02-04-1996)“…The central role of cyclin-dependent kinases (CDKs) in cell cycle regulation makes them a promising target for studying inhibitory molecules that can modify…”
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Spiculated periosteal response induced by intraosseous injection of 22Rv1 prostate cancer cells resembles subset of bone metastases in prostate cancer patients
Published in The Prostate (01-12-2005)“…Background Prostate cancer bone metastasis is distinguished by the predominance of osteoblastic lesions. This phenotype has been difficult to reproduce in…”
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Antibody-based therapeutics in oncology
Published in Expert review of anticancer therapy (01-02-2003)“…The recent clinical and commercial success of anticancer antibodies, such as rituximab (Rituxan®) and trastuzumab (Herceptin®) has created great interest in…”
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Possible Role for Serine/Threonine Phosphorylation in the Regulation of the Heteroprotein Complex between the hsp90 Stress Protein and the pp60 Tyrosine Kinase
Published in The Journal of biological chemistry (01-12-1995)“…The abundant, cytoplasmic 90-kDa heat-shock protein associates transiently with the Rous sarcoma virus oncogenic protein tyrosine kinase, pp60 , directs its…”
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The Gastrin-releasing Peptide Receptor Is Rapidly Phosphorylated by a Kinase Other Than Protein Kinase C After Exposure to Agonist (∗)
Published in The Journal of biological chemistry (07-04-1995)“…Several guanine nucleotide-binding protein-coupled receptors are known to be rapidly phosphorylated after agonist exposure. In this study we show that the…”
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Possible Role for Serine/Threonine Phosphorylation in the Regulation of the Heteroprotein Complex between the hsp90 Stress Protein and the pp60v-src Tyrosine Kinase ()
Published in The Journal of biological chemistry (01-12-1995)“…The abundant, cytoplasmic 90-kDa heat-shock protein associates transiently with the Rous sarcoma virus oncogenic protein tyrosine kinase, pp60v-src, directs…”
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Radioimmunoassay for the quantitation of lisinopril and enalaprilat
Published in Journal of pharmaceutical sciences (01-05-1986)“…A sensitive radioimmunoassay (RIA) capable of measuring either lisinopril (1-[N2-[(S)-1-carboxy-3-phenylpropyl]-L-lysyl] -L-proline) or enalaprilat…”
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Expression of growth-related genes during tumor progression in v-raf-transformed rat liver epithelial cells
Published in Cancer research (Chicago, Ill.) (01-12-1990)“…Clonal cell lines were derived from rat liver epithelial cells following their transformation with either v-raf or v-raf/v-myc. Cells transformed with v-raf…”
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Potent inhibition of CDC2 kinase activity by the flavonoid L86-8275
Published in Biochemical and biophysical research communications (15-06-1994)“…L86-8275 [(-) cis-5,7-dihydroxy-2-(2-chlorophenyl)-8[4-(3-hydroxy-1- methyl)-piperidinyl]-4H-benzopyran-4-one] directly inhibits immunoprecipitated Cdc2 kinase…”
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Differential inhibition of protein kinase C isozymes by UCN-01, a staurosporine analogue
Published in Molecular pharmacology (01-06-1994)“…UCN-01 (7-hydroxystaurosporine) has been demonstrated to be a potent inhibitor of tumor cell growth both in cell culture and with in vivo xenograft models. The…”
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Structure-activity relationship studies of flavopiridol analogues
Published in Bioorganic & medicinal chemistry letters (15-05-2000)“…Cyclin dependent kinases (CDKs) along with the complementary cyclins form key regulatory checkpoint controls on the cell cycle. Flavopiridol is a synthetic…”
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Potentiation of human vascular smooth muscle contraction by angiotensin
Published in Journal of cardiovascular pharmacology (01-07-1980)Get more information
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Cell cycle arrest and growth inhibition by the protein kinase antagonist UCN-01 in human breast carcinoma cells
Published in Cancer research (Chicago, Ill.) (01-05-1993)“…UCN-01 is a derivative of staurosporine, initially developed as a potentially selective inhibitor of the Ca(2+)- and phospholipid-dependent protein kinase C,…”
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