Zobrazeno 1 - 10
of 55
pro vyhledávání: '"W S, Dalton"'
Autor:
J. Doroshow, E. T. Liu, M. Pellini, V. Miller, G. Palmer, S. Averbuch, G. Green, J. Novotny, P. Paoletti, K. Patel, A. Hoos, R. Gaynor, S. Melemed, C. Reinhard, B. T. Teh, W. K. Hong, E. Kim, R. Herbst, V. Papadimitrakopoulou, K. Gold, I. Wistuba, J. Lee, S. Lippman, J. R. Jackson, L. Zitvogel, C. Meisel, P. Workman, W. S. Dalton, N. Botwood, B. J. Davis, G. Batist, S. Assouline, E. Camlioglu, B. Tetu, A. Spatz, Z. Diaz, A. Aguilar-Mahecha, M. Basik, J. Rodon, R. Dienstmann, J. Cortes, C. Saura, C. Aura, J. Hernandez-Losa, A. Vivancos, J. Joan, J. del Campo, E. Felip, J. Seoane, J. T. Tabernero, S. H. Friend, A. M. Tsimberidou, D. S. Hong, J. J. Wheler, Y. Ye, S. Fu, S. A. Piha-Paul, A. Naing, G. S. Falchook, F. Janku, R. Luthra, S. Wen, R. Kurzrock, M. Naley, P. Johnson, K. Schuerer, M. Lopes, L. E. Hood, Y. Yarden, J. Quackenbush
Publikováno v:
Annals of Oncology. 23:v6-v11
Publikováno v:
Hematology. 2001:157-177
Multiple myeloma (MM) is a malignancy of the plasma cell characterized by migration and localization to the bone marrow where cells then disseminate and facilitate the formation of bone lesions. Unfortunately, while treatment of this disease is effec
Publikováno v:
Blood. 78:44-50
Verapamil was evaluated as a chemosensitizer for reversing multidrug resistance in multiple myeloma both in vitro and in clinical trials. Bone marrows from 59 myeloma patients in relapse were evaluated for several resistance parameters: expression of
Autor:
K H, Shain, W S, Dalton
Publikováno v:
Molecular cancer therapeutics. 1(1)
Clinical circumvention of multidrug resistance (MDR) is a Sisyphian task faced in the treatment of many cancers. Identification of several mechanisms of acquired MDR has led to the development of chemosensitizing agents that counter specific mechanis
Autor:
L A, Hazlehurst, W S, Dalton
Publikováno v:
Cancer metastasis reviews. 20(1-2)
The tumor microenvironment is often overlooked when considering tumor response to chemotherapeutic agents. This environment consists of soluble factors, components of the extracellular matrix as well as cell-cell interactions. Recently, it has become
Autor:
M M, Oshiro, T H, Landowski, R, Catlett-Falcone, L A, Hazlehurst, M, Huang, R, Jove, W S, Dalton
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 7(12)
Our previous work demonstrated that the Janus kinase (JAK)-Stat3 pathway regulates expression of Bcl-x(L) in the U266 human multiple myeloma cell line and prevents Fas-mediated apoptosis. Inhibition of this pathway by the JAK selective kinase inhibit
Publikováno v:
Cancer research. 61(8)
Gene therapy of B16 tumors with a dominant-negative signal transducer and activator of transcription (Stat3) variant, designated Stat3beta, results in inhibition of tumor growth and tumor regression. Although only 10-15% of the tumor cells are transf
Autor:
M N, Fishman, W S, Dalton
Publikováno v:
Oncology (Williston Park, N.Y.). 14(11A)
Multiple myeloma remains an incurable cancer. In recent years, progress in different drug classes has improved outcomes, but management has become more complicated. Areas such as prognostic classification, the increased use of high-dose chemotherapy
Autor:
K, Kudoh, M, Ramanna, R, Ravatn, A G, Elkahloun, M L, Bittner, P S, Meltzer, J M, Trent, W S, Dalton, K V, Chin
Publikováno v:
Cancer research. 60(15)
Drug resistance in cancer is a major obstacle to successful chemotherapy. Cancer cells exposed to antitumor drugs may be directly induced to express a subset of genes that could confer resistance, thus allowing some cells to escape killing and form t
Autor:
G L, Scheffer, M, Maliepaard, A C, Pijnenborg, M A, van Gastelen, M C, de Jong, A B, Schroeijers, D M, van der Kolk, J D, Allen, D D, Ross, P, van der Valk, W S, Dalton, J H, Schellens, R J, Scheper
Publikováno v:
Cancer research. 60(10)
Tumor cells may display a multidrug resistant phenotype by overexpression of ATP-binding cassette transporters such as multidrug resistance (MDRI) P-glycoprotein, multidrug resistance protein 1 (MRP1), and breast cancer resistance protein (BCRP). The