Search Results - "Munster, P N"

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    A phase II study of the histone deacetylase inhibitor vorinostat combined with tamoxifen for the treatment of patients with hormone therapy-resistant breast cancer by Munster, P N, Thurn, K T, Thomas, S, Raha, P, Lacevic, M, Miller, A, Melisko, M, Ismail-Khan, R, Rugo, H, Moasser, M, Minton, S E

    Published in British journal of cancer (07-06-2011)
    “…Background: Histone deacetylases (HDACs) are crucial components of the oestrogen receptor (ER) transcriptional complex. Preclinically, HDAC inhibitors can…”
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    Phase II study of single-agent bosutinib, a Src/Abl tyrosine kinase inhibitor, in patients with locally advanced or metastatic breast cancer pretreated with chemotherapy by Campone, M., Bondarenko, I., Brincat, S., Hotko, Y., Munster, P.N., Chmielowska, E., Fumoleau, P., Ward, R., Bardy-Bouxin, N., Leip, E., Turnbull, K., Zacharchuk, C., Epstein, R.J.

    Published in Annals of oncology (01-03-2012)
    “…This phase II study evaluated single-agent bosutinib in pretreated patients with locally advanced or metastatic breast cancer. Patients received oral bosutinib…”
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    Phase I clinical trial of the Src inhibitor dasatinib with dacarbazine in metastatic melanoma by Algazi, A P, Weber, J S, Andrews, S C, Urbas, P, Munster, P N, DeConti, R C, Hwang, J, Sondak, V K, Messina, J L, McCalmont, T, Daud, A I

    Published in British journal of cancer (03-01-2012)
    “…Background: Src inhibitors sensitise melanoma cells to chemotherapy in preclinical models. The combination of dasatinib and dacarbazine was tested in a phase I…”
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    Results of a phase 1 trial combining ridaforolimus and MK-0752 in patients with advanced solid tumours by Piha-Paul, S.A, Munster, P.N, Hollebecque, A, Argilés, G, Dajani, O, Cheng, J.D, Wang, R, Swift, A, Tosolini, A, Gupta, S

    Published in European journal of cancer (1990) (01-09-2015)
    “…Abstract Background The phosphatidylinositol 3-kinase/protein kinase-B/mammalian target of rapamycin (PI3K-AKT-mTOR) signalling pathway is aberrantly activated…”
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    Phase I trial of vorinostat and doxorubicin in solid tumours: histone deacetylase 2 expression as a predictive marker by Munster, P N, Marchion, D, Thomas, S, Egorin, M, Minton, S, Springett, G, Lee, J-H, Simon, G, Chiappori, A, Sullivan, D, Daud, A

    Published in British journal of cancer (06-10-2009)
    “…Background: Histone deacetylase inhibitors (HDACi) can sensitise cancer cells to topoisomerase inhibitors by increasing their access and binding to DNA…”
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    A phase I trial of panobinostat and epirubicin in solid tumors with a dose expansion in patients with sarcoma by Thomas, S., Aggarwal, R., Jahan, T., Ryan, C., Troung, T., Cripps, A.M., Raha, P., Thurn, K.T., Chen, S., Grabowsky, J.A., Park, J., Hwang, J., Daud, A., Munster, P.N.

    Published in Annals of oncology (01-05-2016)
    “…Treatment options for sarcoma are limited. Histone deacetylase inhibitors increase the efficacy of topoisomerase II inhibitors by promoting access to chromatin…”
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    Identification of a geldanamycin dimer that induces the selective degradation of HER-family tyrosine kinases by ZHENG, F. F, KUDUK, S. D, CHIOSIS, G, MÜNSTER, P. N, SEPP-LORENZINO, L, DANISHEFSKY, S. J, ROSEN, N

    Published in Cancer research (Chicago, Ill.) (15-04-2000)
    “…Geldanamycin (GM) is a natural antibiotic that binds Hsp90 and induces the degradation of receptor tyrosine kinases, steroid receptors, and Raf. It is a potent…”
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    Phase I Study of a Third-Generation Selective Estrogen Receptor Modulator, LY353381.HCl, in Metastatic Breast Cancer by Münster, P N, Buzdar, A, Dhingra, K, Enas, N, Ni, L, Major, M, Melemed, A, Seidman, A, Booser, D, Theriault, R, Norton, L, Hudis, C

    Published in Journal of clinical oncology (01-04-2001)
    “…We conducted this phase I trial to determine the safety and toxicity profile of LY353381.HCl-a novel, potent, third-generation selective estrogen receptor…”
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    The histone deacetylase inhibitor suberoylanilide hydroxamic acid induces differentiation of human breast cancer cells by MUNSTER, Pamela N, TROSO-SANDOVAL, Tiffany, ROSEN, Neal, RIFKIND, Richard, MARKS, Paul A, RICHON, Victoria M

    Published in Cancer research (Chicago, Ill.) (01-12-2001)
    “…Histone deacetylase (HDACs) regulate histone acetylation by catalyzing the removal of acetyl groups on the NH(2)-terminal lysine residues of the core…”
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    Inhibition of heat shock protein 90 function by ansamycins causes the morphological and functional differentiation of breast cancer cells by MÜNSTER, Pamela N, SRETHAPAKDI, Mary, MOASSER, Mark M, ROSEN, Neal

    Published in Cancer research (Chicago, Ill.) (01-04-2001)
    “…17-(Allylamino)-17-demethoxygeldanamycin (17-AAG) is an ansamycin antibiotic that binds to a conserved pocket in Hsp90 and induces the degradation of proteins…”
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    Arzoxifene: the development and clinical outcome of an ideal SERM by Munster, Pamela N

    Published in Expert opinion on investigational drugs (01-03-2006)
    “…Hormone-sensitive tumours are among the most common cancers in women. Specific inhibition of the estrogen receptor by selective estrogen receptor…”
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    Predictive factor for the response to adjuvant therapy with emphasis in breast cancer by Munster, P N, Norton, L

    Published in Breast cancer research : BCR (2001)
    “…One of the major challenges of early-stage breast cancer is to select the adjuvant therapy that ensures the most benefits and the least harm for the patient…”
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    High-dose therapy for breast cancer by Hudis, C A, Münster, P N

    Published in Seminars in oncology (01-02-1999)
    “…In recent years, the most frequent indication for high-dose autologous stem-cell-supported chemotherapy in the United States has been breast cancer. This…”
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