Activity of bortezomib in adult de novo and relapsed acute myeloid leukemia

L Gil, J Styczynski, D Dytfeld, R Debski… - Anticancer …, 2007 - ar.iiarjournals.org
Background: Bortezomib is an inhibitor of proteasome and NF-κB, with activity in various
solid tumors and hematological malignancies. Aim: The aim of the study was the analysis of …

Anti-leukemic activity of bortezomib and carfilzomib on B-cell precursor ALL cell lines

K Takahashi, T Inukai, T Imamura, M Yano… - PLoS …, 2017 - journals.plos.org
Prognosis of childhood acute lymphoblastic leukemia (ALL) has been dramatically
improved. However, prognosis of the cases refractory to primary therapy is still poor. Recent …

Bortezomib: proteasome inhibition as an effective anticancer therapy

PG Richardson, C Mitsiades, T Hideshima… - Annu. Rev …, 2006 - annualreviews.org
VELCADE®(bortezomib, Millennium Pharmaceuticals, Inc., Cambridge, MA, and Johnson &
Johnson Pharmaceutical Research & Development, LLC, Raritan, NJ) is a first-in-class …

Evaluating the immunoproteasome as a potential therapeutic target in cisplatin-resistant small cell and non-small cell lung cancer

T Shoji, E Kikuchi, J Kikuchi, Y Takashima… - Cancer chemotherapy …, 2020 - Springer
Purpose We evaluated the expression of proteasome subunits to assess whether the
proteasome could be a therapeutic target in cisplatin-resistant lung cancer cells. Methods …

Differential cellular and molecular effects of bortezomib, a proteasome inhibitor, in human breast cancer cells

J Codony-Servat, MA Tapia, M Bosch, C Oliva… - Molecular cancer …, 2006 - AACR
The cellular and molecular effects of the proteasome inhibitor bortezomib on breast cancer
cells are as yet poorly characterized. Here, in a panel of six breast cancer cell lines …

The proteasome inhibitor bortezomib reverses P-glycoprotein-mediated leukemia multi-drug resistance through the NF-κB pathway

H Wang, X Wang, Y Li, A Liao, B Fu… - Die Pharmazie-An …, 2012 - ingentaconnect.com
Multi-drug resistance (MDR) is one of the obstacles for leukemia therapy, the major cause is
an overexpression of P-glycoprotein (P-gp) leading to increased drug efflux. We investigated …

Effects of the proteasome inhibitor bortezomib alone and in combination with chemotherapeutic agents in gastric cancer cell lines

SH Bae, HM Ryoo, MK Kim, KH Lee… - Oncology …, 2008 - spandidos-publications.com
The proteasome plays a pivotal role in controlling cell proliferation, apoptosis, and
differentiation in a variety of tumor cells. Bortezomib is a boronic acid dipeptide derivative …

Molecular and clinical aspects of proteasome inhibition in the treatment of cancer

I Zavrski, C Jakob, M Kaiser, C Fleissner… - Targeted Therapies in …, 2007 - Springer
The proteasome is a multicatalytic threonine protease responsible for intracellular protein
turnover in eukaryotic cells, including the processing and degradation of several proteins …

Phase I study of bortezomib in refractory or relapsed acute leukemias

J Cortes, D Thomas, C Koller, F Giles, E Estey… - Clinical Cancer …, 2004 - AACR
Abstract Bortezomib (Velcade, formerly PS-341) is proteasome inhibitor with documented
antitumor activity in multiple myeloma and other lymphoid malignancies. We performed a …

Molecular mechanisms of acquired proteasome inhibitor resistance

AJ Kale, BS Moore - Journal of medicinal chemistry, 2012 - ACS Publications
The development of proteasome inhibitors (PIs) has transformed the treatment of multiple
myeloma and mantle cell lymphoma. To date, two PIs have been FDA approved, the …