Research Topics
Species | Min Jean YinSummaryAffiliation: Pfizer Global Research and Development Country: USA Publications
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Detail Information
Publications
Targeting the mTOR Pathway in Tumor MalignancyHengmiao Cheng
Pfizer Worldwide Research and Development, Oncology Research, 10724 Science Center Drive, San Diego, CA 92121, USA
Curr Cancer Drug Targets 13:267-77. 2013..Here we discuss the mechanism of mTOR regulation in tumor malignancy through a variety of signaling pathways and the potential of mTOR inhibitors for the treatment of cancer...
The serine/threonine kinase Nek6 is required for cell cycle progression through mitosisMin Jean Yin
SUGEN, Inc, South San Francisco, California 94080 4811, USA
J Biol Chem 278:52454-60. 2003....
Pharmacokinetic-pharmacodynamic modeling of biomarker response and tumor growth inhibition to an orally available heat shock protein 90 inhibitor in a human tumor xenograft mouse modelShinji Yamazaki
Department of Pharmacokinetics, Pfizer Worldwide Research and Development, San Diego, California 92121, USA
J Pharmacol Exp Ther 338:964-73. 2011..The present results will be helpful in determining the appropriate dosing regimen and guiding dose escalation to achieve efficacious systemic exposure in the clinic...
Effective targeting of triple-negative breast cancer cells by PF-4942847, a novel oral inhibitor of Hsp 90Pramod P Mehta
Oncology Research, Pfizer Worldwide Research and Development, San Diego, California 92121, USA
Clin Cancer Res 17:5432-42. 2011..Therefore, an Hsp90 inhibitor may show therapeutic benefit in TNBC by targeting multiple pathways...
Targeting 3-phosphoinoside-dependent kinase-1 to inhibit insulin-like growth factor-I induced AKT and p70 S6 kinase activation in breast cancer cellsSangita M Baxi
Oncology Research, Pfizer Worldwide Research and Development, San Diego, California, United States of America
PLoS ONE 7:e48402. 2012..These results may provide insight into clinical strategies for developing an IGFR-I inhibitor and/or a PDK1 inhibitor in luminal breast cancer patients...
PF-04691502, a potent and selective oral inhibitor of PI3K and mTOR kinases with antitumor activityJing Yuan
Oncology Research Unit, Pfizer Worldwide Research and Development, La Jolla Laboratories, San Diego, CA 92121, USA
Mol Cancer Ther 10:2189-99. 2011..In summary, PF-04691502 is a potent dual PI3K/mTOR inhibitor with broad antitumor activity. PF-04691502 has entered phase I clinical trials...
Nek6 mediates human cancer cell transformation and is a potential cancer therapeutic targetRounak Nassirpour
Pfizer Global Research and Development, La Jolla Laboratories, 10724 Science Center Drive, San Diego, CA 92121, USA
Mol Cancer Res 8:717-28. 2010..Taken together, our data indicate a pivotal role for Nek6 in tumorigenesis and establish Nek6 as a potential target for treatment of a variety of human cancers...
A novel class of specific Hsp90 small molecule inhibitors demonstrate in vitro and in vivo anti-tumor activity in human melanoma cellsPramod P Mehta
Pfizer Worldwide Research and Development, Oncology Research, 10724 Science Center Drive, San Diego, CA 92121, United States
Cancer Lett 300:30-9. 2011..Our results indicate that Hsp90 inhibitors induce anti-tumor activity in melanoma cells and are likely to show therapeutic benefit in melanoma patients by collaboratively targeting multiple pathways...
Dihydroxyphenylisoindoline amides as orally bioavailable inhibitors of the heat shock protein 90 (hsp90) molecular chaperonePei Pei Kung
Pfizer Global Research and Development, La Jolla Laboratories, 10770 Science Center Drive, San Diego, California 92121, USA
J Med Chem 53:499-503. 2010..This class is exemplified by 14 and 15, which possess improved cell potency and pharmacokinetic profiles compared with the original screening hit...
Dihydroxylphenyl amides as inhibitors of the Hsp90 molecular chaperonePei Pei Kung
Pfizer Global Research and Development, La Jolla Laboratories, 10770, Science Center Dr, San Diego, CA 92121, USA
Bioorg Med Chem Lett 18:6273-8. 2008..Enantio-pure compounds 31 and 33 were potent in PGA-based competitive binding assay and inhibited proliferation of various human cancer cell lines in vitro, with IC(50) values averaging 20 nM...
Optimization of potent, selective, and orally bioavailable pyrrolodinopyrimidine-containing inhibitors of heat shock protein 90. Identification of development candidate 2-amino-4-{4-chloro-2-[2-(4-fluoro-1H-pyrazol-1-yl)ethoxy]-6-methylphenyl}-N-(2,2-diflLuke Zehnder
La Jolla Laboratories, Pfizer Worldwide Research and Development, 10770 Science Center Drive, San Diego, California 92121, United States
J Med Chem 54:3368-85. 2011..These efforts culminated with the identification of a development candidate (compound 42) which displayed desired PK/PD relationships, significant efficacy in a melanoma A2058 xenograft tumor model, and attractive DMPK profiles...
