A novel proteasome inhibitor NPI-0052 as an anticancer therapy

D Chauhan, T Hideshima, KC Anderson - British Journal of Cancer, 2006 - nature.com
Abstract Proteasome inhibitor Bortezomib/Velcade has emerged as an effective anticancer
therapy for the treatment of relapsed and/or refractory multiple myeloma (MM), but prolonged …

Bortezomib: efficacy comparisons in solid tumors and hematologic malignancies

T Caravita, P De Fabritiis, A Palumbo… - Nature clinical practice …, 2006 - nature.com
Proteasome inhibition represents a new anticancer approach, with the potential effect of
arresting tumor growth, metastasis and angiogenesis through the activation of multiple …

Preclinical evaluation of the proteasome inhibitor bortezomib in cancer therapy

M Boccadoro, G Morgan, J Cavenagh - Cancer cell international, 2005 - Springer
Bortezomib is a highly selective, reversible inhibitor of the 26S proteasome that is indicated
for single-agent use in the treatment of patients with multiple myeloma who have received at …

[HTML][HTML] The development of proteasome inhibitors as anticancer drugs

J Adams - Cancer cell, 2004 - cell.com
The ubiquitin-proteasome pathway plays a central role in the targeted destruction of cellular
proteins, including cell cycle regulatory proteins. Because these pathways are critical for the …

Bortezomib as the first proteasome inhibitor anticancer drug: current status and future perspectives

D Chen, M Frezza, S Schmitt, J Kanwar… - Current cancer drug …, 2011 - ingentaconnect.com
Targeting the ubiquitin-proteasome pathway has emerged as a rational approach in the
treatment of human cancer. Based on positive preclinical and clinical studies, bortezomib …

Bortezomib: a review of its use in patients with multiple myeloma

MP Curran, K McKeage - Drugs, 2009 - Springer
Bortezomib (VELCADE®) is a proteasome inhibitor that not only targets the myeloma cell,
but also acts in the bone marrow micro-environment, inhibiting the binding of myeloma cells …

Bortezomib: a novel therapy approved for multiple myeloma.

PG Richardson, KC Anderson - Clinical Advances in Hematology & …, 2003 - europepmc.org
Cellular homeostasis requires routine degradation of key regulatory proteins, including
tumor suppressor gene products, transcription factors, cell-cycle proteins and their inhibitors …

Clinical factors predictive of outcome with bortezomib in patients with relapsed, refractory multiple myeloma

PGG Richardson, B Barlogie, J Berenson, S Singhal… - Blood, 2005 - ashpublications.org
Bortezomib, a potent and reversible proteasome inhibitor, affects the myeloma cell and its
microenvironment, resulting in down-regulation of growth and survival signaling pathways …

A novel orally active proteasome inhibitor ONX 0912 triggers in vitro and in vivo cytotoxicity in multiple myeloma

D Chauhan, AV Singh, M Aujay, CJ Kirk… - Blood, The Journal …, 2010 - ashpublications.org
Bortezomib therapy has proven successful for the treatment of relapsed, relapsed/refractory,
and newly diagnosed multiple myeloma (MM). At present, bortezomib is available as an …

Proteasome inhibition and its clinical prospects in the treatment of hematologic and solid malignancies

H Ludwig, D Khayat, G Giaccone… - … International Journal of …, 2005 - Wiley Online Library
The proteasome is responsible for the degradation of intracellular proteins, including several
involved in cell cycle control and the regulation of apoptosis. Preclinical studies have shown …