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The PP242 Mammalian Target of Rapamycin (mTOR) Inhibitor Activates Extracellular Signal-regulated Kinase (ERK) in Multiple Myeloma Cells via a Target of Rapamycin Complex 1 (TORC1)/ Eukaryotic Translation Initiation Factor 4E (eIF-4E)/RAF Pathway and Activation Is a Mechanism of Resistance

Activation of PI3-K-AKT and ERK pathways is a complication of mTOR inhibitor therapy. Newer mTOR inhibitors (like pp242) can overcome feedback activation of AKT in multiple myeloma (MM) cells. We, thus, studied if feedback activation of ERK is still a complication of therapy with such drugs in this...

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Detaylı Bibliyografya
Asıl Yazarlar: Hoang, Bao, Benavides, Angelica, Shi, Yijiang, Yang, Yonghui, Frost, Patrick, Gera, Joseph, Lichtenstein, Alan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Biochemistry and Molecular Biology 2012
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3381142/
https://ncbi.nlm.nih.gov/pubmed/22556409
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M111.304626
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