Role of the phosphatidylinositol 3-kinase/Akt and mTOR/P70S6-kinase pathways in the proliferation and apoptosis in multiple myeloma.
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CCL5-mediated T-cell chemotaxis involves the initiation of mRNA translation through mTOR/4E-BP1Mammalian target of rapamycin: a central node of complex signaling cascadesClinical and translational studies of a phase II trial of the novel oral Akt inhibitor perifosine in relapsed or relapsed/refractory Waldenstrom's macroglobulinemiaNovel therapeutic strategies for multiple myelomaThe Akt pathway regulates survival and homing in Waldenstrom macroglobulinemiaTargeting NF-kappaB in Waldenstrom macroglobulinemiaProteomic Characterization of the World Trade Center dust-activated mdig and c-myc signaling circuit linked to multiple myelomaThe Mu opioid receptor promotes opioid and growth factor-induced proliferation, migration and Epithelial Mesenchymal Transition (EMT) in human lung cancerCyclin D1 induction by benzo[a]pyrene-7,8-diol-9,10-epoxide via the phosphatidylinositol 3-kinase/Akt/MAPK- and p70s6k-dependent pathway promotes cell transformation and tumorigenesisInhibition of IGF-1 signalling enhances the apoptotic effect of AS602868, an IKK2 inhibitor, in multiple myeloma cell lines.Phase II trial of temsirolimus in patients with relapsed or refractory multiple myeloma.Long-term results of the phase II trial of the oral mTOR inhibitor everolimus (RAD001) in relapsed or refractory Waldenstrom Macroglobulinemia.TAK-228 (formerly MLN0128), an investigational dual TORC1/2 inhibitor plus paclitaxel, with/without trastuzumab, in patients with advanced solid malignancies.Phase II trial of the oral mammalian target of rapamycin inhibitor everolimus in relapsed or refractory Waldenstrom macroglobulinemia.MLN4924, an NAE inhibitor, suppresses AKT and mTOR signaling via upregulation of REDD1 in human myeloma cells.CD28-mediated pro-survival signaling induces chemotherapeutic resistance in multiple myelomaPDK1 inhibitor GSK2334470 exerts antitumor activity in multiple myeloma and forms a novel multitargeted combination with dual mTORC1/C2 inhibitor PP242Transcriptome analysis reveals molecular profiles associated with evolving steps of monoclonal gammopathies.Selective and potent Akt inhibition triggers anti-myeloma activities and enhances fatal endoplasmic reticulum stress induced by proteasome inhibition.Role of dual PI3/Akt and mTOR inhibition in Waldenstrom's Macroglobulinemia.Inhibition of sphingosine kinase 2 downregulates the expression of c-Myc and Mcl-1 and induces apoptosis in multiple myeloma.Frap, FKBP12 rapamycin-associated protein, is a candidate gene for the plasmacytoma resistance locus Pctr2 and can act as a tumor suppressor geneNovel phosphatidylinositol 3-kinase inhibitor NVP-BKM120 induces apoptosis in myeloma cells and shows synergistic anti-myeloma activity with dexamethasone.Targeted inhibition of interleukin-6 with CNTO 328 sensitizes pre-clinical models of multiple myeloma to dexamethasone-mediated cell death.Dual blocking of mTor and PI3K elicits a prodifferentiation effect on glioblastoma stem-like cells.The CXCR4 Antagonist AMD3100 Has Dual Effects on Survival and Proliferation of Myeloma Cells In Vitro.New insights, recent advances, and current challenges in the biological treatment of multiple myeloma.The mTOR pathway affects proliferation and chemosensitivity of urothelial carcinoma cells and is upregulated in a subset of human bladder cancers.Quantitative phosphoproteomic analysis identifies activation of the RET and IGF-1R/IR signaling pathways in neuroblastoma.The use of novel agents in the treatment of relapsed and refractory multiple myelomaSurvival and proliferation factors of normal and malignant plasma cells.Activity of everolimus (RAD001) in relapsed and/or refractory multiple myeloma: a phase I study.Loss of serum and glucocorticoid-regulated kinase 3 (SGK3) does not affect proliferation and survival of multiple myeloma cell linesThe mTOR inhibitor rapamycin down-regulates the expression of the ubiquitin ligase subunit Skp2 in breast cancer cells.Skp2 is a promising therapeutic target in breast cancer.SC06, a novel small molecule compound, displays preclinical activity against multiple myeloma by disrupting the mTOR signaling pathwaySurface chemistry but not aspect ratio mediates the biological toxicity of gold nanorods in vitro and in vivo.Expression and clinical significance of mammalian target of rapamycin/P70 ribosomal protein S6 kinase signaling pathway in human colorectal carcinoma tissue.Constitutive activation of Akt contributes to the pathogenesis and survival of mantle cell lymphoma.Avian Reovirus Protein p17 Functions as a Nucleoporin Tpr Suppressor Leading to Activation of p53, p21 and PTEN and Inactivation of PI3K/AKT/mTOR and ERK Signaling Pathways.
P2860
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P2860
Role of the phosphatidylinositol 3-kinase/Akt and mTOR/P70S6-kinase pathways in the proliferation and apoptosis in multiple myeloma.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
2002年论文
@zh
2002年论文
@zh-cn
name
Role of the phosphatidylinosit ...... apoptosis in multiple myeloma.
@en
type
label
Role of the phosphatidylinosit ...... apoptosis in multiple myeloma.
@en
prefLabel
Role of the phosphatidylinosit ...... apoptosis in multiple myeloma.
@en
P2093
P2860
P356
P1433
P1476
Role of the phosphatidylinosit ...... apoptosis in multiple myeloma.
@en
P2093
Catherine Lacombe
Didier Bouscary
Franck Viguié
François Dreyfus
Frédéric Pene
Odile Muller
Patrick Mayeux
Yann-Erick Claessens
P2860
P2888
P304
P356
10.1038/SJ.ONC.1205923
P407
P577
2002-09-01T00:00:00Z
P5875
P6179
1007035873