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									<identifier>oai:www.peertechzpublications.org:10.17352/gjct.000007</identifier>
									<datestamp>2016-03-08</datestamp>
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										Bortezomib in Anti-Cancer Activity: A Potential Drug
										</dc:title><dc:creator>Rajagopal Appavu</dc:creator><dc:creator>Deepa Mohan</dc:creator><dc:description>&lt;p&gt;26S proteasome is an intracellular; ATP dependent enzymatic complex degrades ubiquitin-tagged
proteins and maintains cellular homeostasis. The orderly degraded proteins including cyclins, caspases,
Bcl-xL, p53, cell adhesion molecules are involved in cell-cycle progression, tumor suppression, DNA
replication, inflammation, and apoptosis. So, proteasome inhibition is a target therapy for cancer to
promote cell cycle arrest or apoptosis. Bortezomib (Velcade®, PS-341, and Millennium Pharmaceuticals,
Inc.) is the first, selective, reversible, and only proteasome inhibitor for the treatment of multiple myeloma
have been approved by U.S. Food and Drug Administration (FDA) in 2003. Bortezomib downregulates
the interaction of multiple myeloma cells with bone marrow stromal cells, inhibits angiogenesis, and
blocks cell cycle progression. Clinically, continuous dosage of bortezomib leads to few side effects.&lt;/p&gt;</dc:description>
										<dc:publisher>Global Journal of Cancer Therapy - Peertechz Publications</dc:publisher>
										<dc:date>2016-03-08</dc:date>
										<dc:type>Mini Review</dc:type>
										<dc:identifier>https://doi.org/10.17352/gjct.000007</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Rajagopal Appavu et al.</dc:rights>
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