Targeting c-MYC by antagonizing PP2A inhibitors in breast cancer.
about
The broken "Off" switch in cancer signaling: PP2A as a regulator of tumorigenesis, drug resistance, and immune surveillanceProtein Phosphatase 2A as a Therapeutic Target in Acute Myeloid LeukemiaSIRT3 inhibits prostate cancer by destabilizing oncoprotein c-MYC through regulation of the PI3K/Akt pathway.Computer-aided targeting of the PI3K/Akt/mTOR pathway: toxicity reduction and therapeutic opportunitiesActivation of tumor suppressor protein PP2A inhibits KRAS-driven tumor growth.The role of SET/I2PP2A in canine mammary tumors.Phorbol esters in seed oil of Jatropha curcas L. (saboodam in Thai) and their association with cancer prevention: from the initial investigation to the present topics.Altered PPP2R2A and Cyclin D1 expression defines a subgroup of aggressive luminal-like breast cancer.PP2A inhibition determines poor outcome and doxorubicin resistance in early breast cancer and its activation shows promising therapeutic effectsOverexpression of PP2A inhibitor SET oncoprotein is associated with tumor progression and poor prognosis in human non-small cell lung cancer.Lithium Chloride Promotes Apoptosis in Human Leukemia NB4 Cells by Inhibiting Glycogen Synthase Kinase-3 Beta.Inhibition of Pten deficient Castration Resistant Prostate Cancer by Targeting of the SET - PP2A Signaling axis.Strategies to Inhibit Myc and Their Clinical ApplicabilityNorcantharidin inhibits renal interstitial fibrosis by downregulating PP2Ac expression.SET antagonist enhances the chemosensitivity of non-small cell lung cancer cells by reactivating protein phosphatase 2AZinc Finger and X-Linked Factor (ZFX) Binds to Human SET Transcript 2 Promoter and Transactivates SET Expression.Combined targeting of SET and tyrosine kinases provides an effective therapeutic approach in human T-cell acute lymphoblastic leukemia.Clinical significance of cancerous inhibitor of protein phosphatase 2A in human cancers.OP449 inhibits breast cancer growth without adverse metabolic effects.All roads lead to PP2A: exploiting the therapeutic potential of this phosphatase.Reprogramming the oncogenic response: SET protein as a potential therapeutic target in cancer.SET/I2PP2A overexpression induces phenotypic, molecular, and metabolic alterations in an oral keratinocyte cell line.PROTOCADHERIN 7 Acts through SET and PP2A to Potentiate MAPK Signaling by EGFR and KRAS during Lung Tumorigenesis.The therapeutic effects of SET/I2PP2A inhibitors on canine melanoma.SCP1 regulates c-Myc stability and functions through dephosphorylating c-Myc Ser62.Leucine-rich repeat-containing protein 59 mediates nuclear import of cancerous inhibitor of PP2A in prostate cancer cells.Cip2a promotes cell cycle progression in triple-negative breast cancer cells by regulating the expression and nuclear export of p27Kip1.MYC Modulation around the CDK2/p27/SKP2 AxisMYC-dependent recruitment of RUNX1 and GATA2 on the SET oncogene promoter enhances PP2A inactivation in acute myeloid leukemia.Directional Migration in Esophageal Squamous Cell Carcinoma (ESCC) is Epigenetically Regulated by SET Nuclear Oncogene, a Member of the Inhibitor of Histone Acetyltransferase Complex.Isoliensinine induces dephosphorylation of NF-kB p65 subunit at Ser536 via a PP2A-dependent mechanism in hepatocellular carcinoma cells: roles of impairing PP2A/I2PP2A interaction.SET contributes to the epithelial-mesenchymal transition of pancreatic cancer.MYC regulates ductal-neuroendocrine lineage plasticity in pancreatic ductal adenocarcinoma associated with poor outcome and chemoresistance.PP2A as the Main Node of Therapeutic Strategies and Resistance Reversal in Triple-Negative Breast Cancer.Therapeutic Targeting of PP2A.Functional importance of PP2A regulatory subunit loss in breast cancer.Loss of protein phosphatase 2A regulatory subunit B56δ promotes spontaneous tumorigenesis in vivo.Upregulation of the oncoprotein SET determines poor clinical outcomes in hepatocellular carcinoma and shows therapeutic potential.Effect of matrine against breast cancer by downregulating the vascular endothelial growth factor via the Wnt/β-catenin pathway.Small molecule activators of protein phosphatase 2A for the treatment of castration-resistant prostate cancer.
P2860
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P2860
Targeting c-MYC by antagonizing PP2A inhibitors in breast cancer.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Targeting c-MYC by antagonizing PP2A inhibitors in breast cancer.
@ast
Targeting c-MYC by antagonizing PP2A inhibitors in breast cancer.
@en
type
label
Targeting c-MYC by antagonizing PP2A inhibitors in breast cancer.
@ast
Targeting c-MYC by antagonizing PP2A inhibitors in breast cancer.
@en
prefLabel
Targeting c-MYC by antagonizing PP2A inhibitors in breast cancer.
@ast
Targeting c-MYC by antagonizing PP2A inhibitors in breast cancer.
@en
P2093
P2860
P356
P1476
Targeting c-MYC by antagonizing PP2A inhibitors in breast cancer.
@en
P2093
Amy S Farrell
Colin J Daniel
Dale J Christensen
Ellen M Langer
Jessica Oddo
Mahnaz Janghorban
Rosalie C Sears
P2860
P304
P356
10.1073/PNAS.1317630111
P407
P577
2014-06-09T00:00:00Z