PRMT5 is required for lymphomagenesis triggered by multiple oncogenic drivers
about
Novel Molecular Markers for Breast CancerTargeting CDK4 and CDK6: From Discovery to TherapyPRMT5-Mediated Methylation of NF-κB p65 at Arg174 Is Required for Endothelial CXCL11 Gene Induction in Response to TNF-α and IFN-γ CostimulationPERK Is a Haploinsufficient Tumor Suppressor: Gene Dose Determines Tumor-Suppressive Versus Tumor Promoting Properties of PERK in Melanoma.Aberrant expression of cyclin D1 in cancer.The protein arginine methyltransferase 5 promotes malignant phenotype of hepatocellular carcinoma cells and is associated with adverse patient outcomes after curative hepatectomyPRMT5-Selective Inhibitors Suppress Inflammatory T Cell Responses and Experimental Autoimmune Encephalomyelitis.The Fanconi anemia pathway controls oncogenic response in hematopoietic stem and progenitor cells by regulating PRMT5-mediated p53 arginine methylation.Post-translational control of transcription factors: methylation ranks highly.CDK6-a review of the past and a glimpse into the future: from cell-cycle control to transcriptional regulation.Beyond transcription factors: how oncogenic signalling reshapes the epigenetic landscape.A TGFβ-PRMT5-MEP50 axis regulates cancer cell invasion through histone H3 and H4 arginine methylation coupled transcriptional activation and repression.Cyclin D1, cancer progression, and opportunities in cancer treatment.PRMT5-dependent p53 escape in tumorigenesis.Anguilla japonica lectin 1 delivery through adenovirus vector induces apoptotic cancer cell death through interaction with PRMT5.A PERK-miR-211 axis suppresses circadian regulators and protein synthesis to promote cancer cell survival.Protein arginine methyltransferase 5 has prognostic relevance and is a druggable target in multiple myeloma.Targeting protein arginine methyltransferase 5 in disease.The PAF complex regulation of Prmt5 facilitates the progression and maintenance of MLL fusion leukemia.Histone phosphorylation by TRPM6's cleaved kinase attenuates adjacent arginine methylation to regulate gene expression.Genetic deletion or small-molecule inhibition of the arginine methyltransferase PRMT5 exhibit anti-tumoral activity in mouse models of MLL-rearranged AML.Identification of a Novel Protein Arginine Methyltransferase 5 Inhibitor in Non-small Cell Lung Cancer by Structure-Based Virtual Screening.CAPG enhances breast cancer metastasis by competing with PRMT5 to modulate STC-1 transcription.An epigenetic regulator-related score (EpiScore) predicts survival in patients with diffuse large B cell lymphoma and identifies patients who may benefit from epigenetic therapy.Activation of the p53-MDM4 regulatory axis defines the anti-tumour response to PRMT5 inhibition through its role in regulating cellular splicing.
P2860
Q26753160-32CF0007-F0FB-4E18-8A1E-D3A8E3EF9CDBQ28082912-6209D8B6-BCDF-4064-A561-7B75CD6F71B9Q28550383-E6979EA4-820E-4675-A081-E5A0C57AF465Q36224716-FDFD8ADD-D9FF-44BA-9CAE-142FAD1A0E61Q37580471-C218CEF4-D0CA-40EF-AA6F-6A9406864C74Q37588076-2DCF8037-8CED-4CEB-A5FE-4169F1C5C489Q37625481-73B17001-36EE-41F5-AD3F-9CDC186BEE93Q37644979-36695BC8-AE8C-4275-AAB1-8798049EE043Q38592178-F90A0674-01CA-42EA-99E3-43E446D1851EQ38616175-D81D8C6C-8058-45DD-AD10-231E3B28EB8AQ38843250-74145FD2-8A79-4B37-8934-EC0D69D0D361Q38857167-B9036A2D-132A-4AAF-94F5-AB8B9A3212A3Q38970431-ED81427F-D9A2-4A1F-BC29-A67244A5C411Q41893763-7CB5041B-D34C-44F4-9003-FFB25055A5F2Q45884221-E82A1D29-CD55-4CA0-A2D7-CC8C0B8EB28FQ46244712-9B4A8ED0-6815-4804-9E91-228577E8170AQ47381020-BA59027F-B7CE-448A-87FF-ABCCEA196A24Q47404539-47824A40-B85F-41A1-AB85-E9DCA94EB549Q47748522-CB4CF40C-37A3-44AE-A4C2-BC4BE7B75975Q47981534-B5641074-E3B0-42D9-9A49-1E138FE4E093Q50915851-469947E2-E6A6-4538-B398-BD70B2E71706Q52353697-DC8A9E22-F4B7-44AE-BBA5-095031BA13A3Q55093730-758A29A7-8823-475E-816C-642A5067CD77Q55106924-D7FC2643-4EBB-4AB8-891E-26FDB3384C46Q55512206-6A9C3EE9-3566-42ED-87BB-74BFD53915CE
P2860
PRMT5 is required for lymphomagenesis triggered by multiple oncogenic drivers
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
PRMT5 is required for lymphomagenesis triggered by multiple oncogenic drivers
@en
PRMT5 is required for lymphomagenesis triggered by multiple oncogenic drivers
@nl
type
label
PRMT5 is required for lymphomagenesis triggered by multiple oncogenic drivers
@en
PRMT5 is required for lymphomagenesis triggered by multiple oncogenic drivers
@nl
prefLabel
PRMT5 is required for lymphomagenesis triggered by multiple oncogenic drivers
@en
PRMT5 is required for lymphomagenesis triggered by multiple oncogenic drivers
@nl
P2093
P2860
P1433
P1476
PRMT5 is required for lymphomagenesis triggered by multiple oncogenic drivers
@en
P2093
Andres J P Klein-Szanto
Anil K Rustgi
Hiroshi Nakagawa
J Alan Diehl
Mariusz Wasik
Nilesh Chitnis
Shoji Natsugoe
Yoshiaki Kita
P2860
P304
P356
10.1158/2159-8290.CD-14-0625
P577
2015-01-12T00:00:00Z