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dc.contributor.authorAbdollahi, Pegah
dc.contributor.authorKöhn, Maja
dc.contributor.authorBørset, Magne
dc.date.accessioned2021-03-22T10:28:40Z
dc.date.available2021-03-22T10:28:40Z
dc.date.created2021-01-05T12:28:22Z
dc.date.issued2020
dc.identifier.issn0304-3835
dc.identifier.urihttps://hdl.handle.net/11250/2734767
dc.description.abstractMany cell signaling pathways are activated or deactivated by protein tyrosine phosphorylation and dephosphorylation, catalyzed by protein tyrosine kinases (PTKs) and protein tyrosine phosphatases (PTPs), respectively. Even though PTPs are as important as PTKs in this process, their role has been neglected for a long time. Multiple myeloma (MM) is a cancer of plasma cells, which is characterized by production of monoclonal immunoglobulin, anemia and destruction of bone. MM is still incurable with high relapse frequency after treatment. In this review, we highlight the PTPs that were previously described in MM or have a role that can be relevant in a myeloma context. Our purpose is to show that despite the importance of PTPs in MM pathogenesis, many unanswered questions in this field need to be addressed. This might help to detect novel treatment strategies for MM patients.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleProtein tyrosine phosphatases in multiple myelomaen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.journalCancer Lettersen_US
dc.identifier.doi10.1016/j.canlet.2020.11.042
dc.identifier.cristin1865499
dc.description.localcode0304-3835/© 2020 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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