Reversion of multidrug-resistance by proteasome inhibitor bortezomib in K562/DNR cell line

H Wang, Y Li, A Liao, B Fu, W Yang, Z Liu… - Chinese Journal of …, 2011 - Springer
Objective To observe the reversion of multi-drug resistance by proteasome inhibitor
bortezomib in K562/DNR cell line and to analyze the possible mechanism of reversion of …

[HTML][HTML] A Phase 1 Trial of MEC (Mitoxantrone, Etoposide, Cytarabine) in combination with bortezomib for relapsed/refractory acute myeloid leukemia

A Advani, P Elson, ED Hsi, R Davis, M Kalaycio… - Blood, 2012 - Elsevier
Abstract 3595 The overexpression of proteasomes and constitutive activation of NF-KB in
acute myeloid leukemia (AML) cells suggest that proteasome inhibitors (PI) such as …

NF-κB–independent down-regulation of XIAP by bortezomib sensitizes HL B cells against cytotoxic drugs

H Kashkar, A Deggerich, JM Seeger, B Yazdanpanah… - Blood, 2007 - ashpublications.org
The proteasome inhibitor bortezomib has been shown to possess promising antitumor
activity and significant efficacy against a variety of malignancies. Different studies …

The proteasome inhibitors bortezomib and PR‐171 have antiproliferative and proapoptotic effects on primary human acute myeloid leukaemia cells

C Stapnes, AP Døskeland, K Hatfield… - British journal of …, 2007 - Wiley Online Library
Proteasome inhibitors represent a new class of antineoplastic drugs that are considered in
the treatment of haematological malignancies. We compared the effects of the reversible …

Anticancer drug bortezomib increases interleukin-8 expression in human monocytes

S Sanacora, J Urdinez, TP Chang… - … and biophysical research …, 2015 - Elsevier
Bortezomib (BZ) is the first clinically approved proteasome inhibitor that has shown
remarkable anticancer activity in patients with hematological malignancies. However, many …

[HTML][HTML] Enhancing activity and overcoming chemoresistance in hematologic malignancies with bortezomib: preclinical mechanistic studies

N Reddy, MS Czuczman - Annals of oncology, 2010 - Elsevier
Background Proteasome inhibition results in antitumor activity through various mechanisms,
including disruption of cell cycle progression and control, induction of apoptosis, and …

Point mutation of the proteasome β5 subunit gene is an important mechanism of bortezomib resistance in bortezomib-selected variants of Jurkat T cell lymphoblastic …

S Lü, J Yang, X Song, S Gong, H Zhou, L Guo… - … of Pharmacology and …, 2008 - ASPET
To study the mechanism of acquired resistance to bortezomib, a new antitumor drug that is
the first therapeutic proteasome inhibitor, we established a series of bortezomib-resistant T …

[HTML][HTML] Cancerous inhibitor of protein phosphatase 2A determines bortezomib-induced apoptosis in leukemia cells

CY Liu, CW Shiau, HY Kuo, HP Huang, MH Chen… - …, 2013 - ncbi.nlm.nih.gov
The multiple cellular targets affected by proteasome inhibition implicate a potential role for
bortezomib, a first-in-class proteasome inhibitor, in enhancing antitumor activities in …

Antitumor activity and drug interactions of proteasome inhibitor Bortezomib in human high-risk myelodysplastic syndrome cells

J Huang, T Ding, M Yang, H Liu, X Sun, J Jin - International journal of …, 2011 - Springer
The purpose of this study was to investigate the antitumor effects and drug interactions of the
proteasome inhibitor Bortezomib against high-risk myelodysplastic syndrome (MDS) cells in …

Successful T-cell acute lymphoblastic leukemia treatment with proteasome inhibitor bortezomib based on evaluation of nuclear factor-κB activity

X Hu, J Xu, A Sun, Y Shen, G He, F Guo - Leukemia & lymphoma, 2011 - Taylor & Francis
The nuclear factor-κ B (NF-κ B) transcription factor plays a pivotal role in diverse biological
processes including immune responses, inflammation, apoptosis, lymphocyte development …