Chemical ablation of androgen receptor in prostate cancer cells by the histone deacetylase inhibitor LAQ824

L Chen, S Meng, H Wang, P Bali, W Bai, B Li… - Molecular cancer …, 2005 - AACR
Androgen receptor plays a critical role in the development of primary as well as advanced
hormone-refractory prostate cancer. Therefore, ablation of androgen receptor from prostate …

Bag1 directly routes immature BCR-ABL for proteasomal degradation

F Tsukahara, Y Maru - Blood, The Journal of the American …, 2010 - ashpublications.org
Degradation of BCR-ABL oncoproteins by heat shock protein 90 (Hsp90) inhibitors in
chronic myelogenous leukemia is expected to overcome resistance to ABL tyrosine kinase …

Imatinib resistance: obstacles and opportunities

MR Litzow - Archives of pathology & laboratory medicine, 2006 - meridian.allenpress.com
Objective.—To review the current status of resistance to imatinib mesylate (IM) in patients
with chronic myelogenous leukemia, and the obstacles and opportunities presented by the …

Adult soft tissue sarcomas: conventional therapies and molecularly targeted approaches

S Mocellin, CR Rossi, A Brandes, D Nitti - Cancer treatment reviews, 2006 - Elsevier
The therapeutic approach to soft tissue sarcomas (STS) has evolved over the past two
decades based on the results from randomized controlled trials, which are guiding …

Species differences in tumour responses to cancer chemotherapy

J Lawrence, D Cameron… - … Transactions of the …, 2015 - royalsocietypublishing.org
Despite advances in chemotherapy, radiotherapy and targeted drug development, cancer
remains a disease of high morbidity and mortality. The treatment of human cancer patients …

RNAi-based screening of the human kinome identifies Akt-cooperating kinases: a new approach to designing efficacious multitargeted kinase inhibitors

S Morgan-Lappe, KW Woods, Q Li, MG Anderson… - Oncogene, 2006 - nature.com
Tumors comprise genetically heterogeneous cell populations, whose growth and survival
depend on multiple signaling pathways. This has spurred the development of multitargeted …

Synthesis and Src Kinase Inhibitory Activity of 2-Phenyl- and 2-Thienyl-7-phenylaminothieno[3,2-b]pyridine-6-carbonitriles

DH Boschelli, B Wu, AC Barrios Sosa… - Journal of medicinal …, 2005 - ACS Publications
2-Phenyl-7-phenylaminothieno [3, 2-b] pyridine-6-carbonitriles were recently reported to be
inhibitors of Src kinase activity. In this study we present structure− activity relationships for …

BMS-354825: a novel drug with potential for the treatment of imatinib-resistant chronic myeloid leukaemia

SA Doggrell - Expert opinion on investigational drugs, 2005 - Taylor & Francis
The BCR-ABL tyrosine kinase inhibitor imatinib has greatly improved the outcome for
patients with chronic myeloid leukaemia (CML). Unfortunately, mutations causing resistance …

SRC inhibitors as potential therapeutic agents for human cancers.

JG Trevino, JM Summy, GE Gallick - Mini reviews in medicinal …, 2006 - europepmc.org
Selective inhibitors of the Src family of protein tyrosine kinases have been developed as
therapeutic agents for human tumors, some of which are now in various stages of clinical …

[HTML][HTML] MDR1/ABCB1 gene polymorphisms in patients with chronic myeloid leukemia

M Lardo, M Castro, B Moiraghi, F Rojas, N Borda… - Blood …, 2015 - ncbi.nlm.nih.gov
Background Tyrosine kinase inhibitors (TKIs) are the recommended treatment for patients
with chronic myeloid leukemia (CML). The MDR1/ABCB1 gene plays a role in resistance to …