Search Results - "Xia, Zuping"
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1
Impact of nonsynonymous single nucleotide polymorphisms on in-vitro metabolism of exemestane by hepatic cytosolic reductases
Published in Pharmacogenetics and genomics (01-08-2016)“…OBJECTIVEExemestane (EXE) is a potent third-generation aromatase inhibitor used as endocrine therapy in breast cancer treatment and prevention…”
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2
Synthesis and Evaluation of Novel Inhibitors of Pim-1 and Pim-2 Protein Kinases
Published in Journal of medicinal chemistry (08-01-2009)“…The Pim protein kinases are frequently overexpressed in prostate cancer and certain forms of leukemia and lymphoma…”
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3
Pim protein kinases regulate energy metabolism and cell growth
Published in Proceedings of the National Academy of Sciences - PNAS (11-01-2011)“…The serine/threonine Pim kinases are overexpressed in solid cancers and hematologic malignancies and promote cell growth and survival. Here, we find that a…”
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4
A small molecule inhibitor of Pim protein kinases blocks the growth of precursor T-cell lymphoblastic leukemia/lymphoma
Published in Blood (28-01-2010)“…The serine/threonine Pim kinases are up-regulated in specific hematologic neoplasms, and play an important role in key signal transduction pathways, including…”
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5
Discovery and evaluation of inhibitors of human ceramidase
Published in Molecular cancer therapeutics (01-11-2011)“…The ceramide/sphingosine-1-phosphate (S1P) rheostat has been hypothesized to play a critical role in regulating tumor cell fate, with elevated levels of…”
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6
Identification of the 4‑Position of 3‑Alkynyl and 3‑Heteroaromatic Substituted Pyridine Methanamines as a Key Modification Site Eliciting Increased Potency and Enhanced Selectivity for Cytochrome P‑450 2A6 Inhibition
Published in Journal of medicinal chemistry (23-08-2018)“…Cigarette smoking causes nearly one in every five deaths in the United States. The development of a specific inhibitor of cytochrome P450 2A6 (CYP2A6), the…”
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7
Suppression of Ulcerative Colitis in Mice by Orally Available Inhibitors of Sphingosine Kinase
Published in Digestive diseases and sciences (01-04-2008)“…A critical step in the mechanism of action of inflammatory cytokines is the stimulation of sphingolipid metabolism, including activation of sphingosine kinase…”
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8
Novel benzylidene-thiazolidine-2,4-diones inhibit Pim protein kinase activity and induce cell cycle arrest in leukemia and prostate cancer cells
Published in Molecular cancer therapeutics (01-06-2009)“…The Pim protein kinases play important roles in cancer development and progression, including prostate tumors and hematologic malignancies. To investigate the…”
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9
Discovery and characterization of inhibitors of human palmitoyl acyltransferases
Published in Molecular cancer therapeutics (01-07-2006)“…The covalent attachment of palmitate to specific proteins by the action of palmitoyl acyltransferases (PAT) plays critical roles in the biological activities…”
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10
Cellular palmitoylation and trafficking of lipidated peptides
Published in Journal of lipid research (01-08-2007)“…Many important signaling proteins require the posttranslational addition of fatty acid chains for their proper subcellular localization and function. One such…”
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11
Improved synthesis of a fluorogenic ceramidase substrate
Published in Bioorganic & medicinal chemistry (01-02-2010)“…Substantial interest has focused on the roles of sphingolipid metabolizing enzymes in a variety of hyperproliferative and inflammatory diseases. A key family…”
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12
Pharmacokinetics of 3'-O-retinoyl-5-fluoro-2'-deoxyuridine (RFUdR), a dual acting mutually masking prodrug, and its metabolites in tumor bearing mice
Published in Current drug delivery (01-10-2013)“…3'-O-Retinoyl-5-fluoro-2'-deoxyuridine (RFUdR) is a putative dual-acting, mutually-masking (DAMM) prodrug for the treatment of cancer. As part of the proof of…”
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13
Synthesis and Evaluation of Dihydropyrroloquinolines That Selectively Antagonize P-Glycoprotein
Published in Journal of medicinal chemistry (11-03-2004)“…In a search for improved multiple drug resistance (MDR) modulators, we identified a novel series of substituted pyrroloquinolines that selectively inhibits the…”
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14
Cyclohexyl-octahydro-pyrrolo[1,2-a]pyrazine-based inhibitors of human N-myristoyltransferase-1
Published in The Journal of pharmacology and experimental therapeutics (01-04-2004)“…N-myristoyltransferase (NMT) is an emerging therapeutic target that catalyzes the attachment of myristate to the N terminus of an acceptor protein. We have…”
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15
Characterization of Cytosolic Glutathione S -Transferases Involved in the Metabolism of the Aromatase Inhibitor, Exemestane
Published in Drug metabolism and disposition (01-12-2021)“…Exemestane (EXE) is a hormonal therapy used to treat estrogen receptor-positive breast cancer by inhibiting the final step of estrogen biosynthesis catalyzed…”
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16
Role of glutathione‐S‐transferases in the metabolism of the anti‐cancer agent and aromatase inhibitor, exemestane
Published in The FASEB journal (01-04-2018)“…Breast cancer is the most commonly diagnosed cancer in women, with approximately 1 in 8 women in the U.S. developing breast cancer over their lifetime. The…”
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17
Glutathione‐S‐Transferases Represent a Novel Pathway Contributing to the Metabolic Clearance of the Anti‐Cancer Agent and Aromatase Inhibitor, Exemestane
Published in The FASEB journal (01-04-2019)“…Breast Cancer is the second leading cause of cancer death among women in the USA, with estrogen‐receptor positive (ER+) tumors accounting for 75% of breast…”
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18
Cytochrome P450 Enzyme Contributions to the N‐oxide Detoxification Pathway of Tobacco‐Specific Nitrosamines; a Possible Role in Tobacco‐Related Cancer Risk
Published in The FASEB journal (01-04-2019)“…Tobacco‐specific nitrosamines (TSNAs) including 4‐(methylnitrosamino)‐1‐(3‐pyridyl)‐1‐butanone (NNK) are among the most potent carcinogens found in tobacco…”
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19
Identification and Quantification of Novel Major Metabolites of the Steroidal Aromatase Inhibitor, Exemestane
Published in Drug metabolism and disposition (01-12-2018)“…Exemestane (EXE) is an aromatase inhibitor used for the prevention and treatment of estrogen receptor-positive breast cancer. Although the known major…”
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20
In vitro metabolism of exemestane by hepatic cytochrome P450s: impact of nonsynonymous polymorphisms on formation of the active metabolite 17β‐dihydroexemestane
Published in Pharmacology research & perspectives (01-06-2017)“…Exemestane (EXE) is an endocrine therapy commonly used by postmenopausal women with hormone‐responsive breast cancer due to its potency in inhibiting…”
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