microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion - Wikidata - awgldk - TriplyDB

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

http://www.wikidata.org/entity/Q34299534

about

Milk is not just food but most likely a genetic transfection system activating mTORC1 signaling for postnatal growth MicroRNAs as prognostic molecular signatures in renal cell carcinoma: a systematic review and meta-analysis Gallbladder's clear cell renal carcinoma metastasis: A case report.A positive feedback loop involving Erk5 and Akt turns on mesangial cell proliferation in response to PDGF.miR-21 inhibitor suppresses proliferation and migration of nasopharyngeal carcinoma cells through down-regulation of BCL2 expression.microRNA-21-induced dissociation of PDCD4 from rictor contributes to Akt-IKKβ-mTORC1 axis to regulate renal cancer cell invasion.The network of microRNAs, transcription factors, target genes and host genes in human renal cell carcinoma.Pseudogene PTENP1 functions as a competing endogenous RNA to suppress clear-cell renal cell carcinoma progression.miRNA signature of mouse helper T cell hyper-proliferation MicroRNA-21 promotes hepatocellular carcinoma HepG2 cell proliferation through repression of mitogen-activated protein kinase-kinase 3.MicroRNA-21 regulates hTERT via PTEN in hypertrophic scar fibroblasts.TGFβ-induced deptor suppression recruits mTORC1 and not mTORC2 to enhance collagen I (α2) gene expression.Suppression of endothelial nitric oxide synthase expression and endothelial cell proliferation by an intronic 27-ntmiRNA and it's a novel link to AP-1.microRNA-425-5p is upregulated in human gastric cancer and contributes to invasion and metastasis in vitro and in vivo The regulation and function of microRNAs in kidney diseases.MicroRNA-214 Reduces Insulin-like Growth Factor-1 (IGF-1) Receptor Expression and Downstream mTORC1 Signaling in Renal Carcinoma Cells.MicroRNAs as novel therapeutic targets to treat kidney injury and fibrosis.Competing endogenous RNA interplay in cancer: mechanism, methodology, and perspectives.MicroRNAs in renal cell carcinoma: a systematic review of clinical implications (Review).ceRNA in cancer: possible functions and clinical implications.Renal Carcinogenesis, Tumor Heterogeneity, and Reactive Oxygen Species: Tactics Evolved.NFκB-mediated cyclin D1 expression by microRNA-21 influences renal cancer cell proliferation.MicroRNA-1 and MicroRNA-21 Individually Regulate Cellular Growth of Non-malignant and Malignant Renal Cells.Hippo signaling mediates proliferation, invasiveness, and metastatic potential of clear cell renal cell carcinoma.Differential expression of microRNA501-5p affects the aggressiveness of clear cell renal carcinoma.Down-regulation of microRNA-182 and microRNA-183 predicts progression of osteosarcoma.Tyrosines-740/751 of PDGFRβ contribute to the activation of Akt/Hif1α/TGFβ nexus to drive high glucose-induced glomerular mesangial cell hypertrophy.PDGF receptor-β uses Akt/mTORC1 signaling node to promote high glucose-induced renal proximal tubular cell collagen I (α2) expression.MicroRNAs in clear cell renal cell carcinoma: biological functions and applications.Renal Cell Carcinoma: Molecular Aspects

P2860

Q24594618-1525FE0D-5187-4D29-BBA1-B80D65B96AB5 Q26785371-DA5AF7E8-254B-4CF6-A931-E3CA6541DD54 Q30391832-48C86346-CAF3-4C04-B68F-1501E5A0A4A6 Q33701475-DC330BA0-7837-4417-A9D0-FF25F5C81AED Q33898669-55ED0376-5F27-4CDF-ADC2-5ACEDD83F42A Q34257789-28EB43F8-526B-4A1A-9939-94A62B609815 Q34582491-B2BFEEAB-63B1-4448-8367-FC45004C08BA Q34693185-C6C681E9-0E3B-42CC-A1AD-6E4950AE3563 Q34794213-AE0BBF91-73EC-44B0-BA71-C2BC9D0FDD57 Q35013542-B3588EF3-4847-481A-82DF-A62F2D2DD828 Q35166623-4CA4BB46-EA83-47A1-8424-B5B25CC976BE Q35354812-AD8E5460-3737-4F2F-BFD3-86463259634C Q35440105-3E3B9B09-FA1A-44BB-8155-36D70A0E43F1 Q35753974-94E75378-9B28-453F-807E-4B6AE832788B Q36960910-1F266BF3-4631-42B4-A1AB-7E7BB8B0D487 Q37078685-B3F4C0F4-B62C-4476-AA17-9F20EB3211C6 Q37211825-D15882EA-9DBC-4D8A-92AB-FE5F67C77C1B Q38325485-291238A6-FF20-4181-93E6-D4B2167EB730 Q38356005-71639112-8582-4364-A36F-20AC216F165B Q38584497-851BF676-D44F-4C6F-9C42-39C570EFED57 Q38854862-E81EBED3-9FFC-43F5-B7CA-C52DF76BD24B Q39104408-957699C8-EA0C-4A00-BD78-8BFD90E5C9B2 Q41487330-5B5E5B12-C449-40FC-8FDB-9ACCC7A334D8 Q41867443-C61E75C0-86FB-4E5B-A529-D67462BB171A Q41966602-89D9AF54-16C3-416A-8337-AF9479D1DDD1 Q47338569-188CBF35-6098-45F9-A380-499B28D04306 Q47757479-3EFB5BCE-9F61-463A-97A7-1D8075FBD92A Q47911791-B6901054-B52E-47CD-8DEC-F85534AA6804 Q51158837-3B7FD678-EDF4-482E-91D8-93FF5E62D396 Q57178229-A6786772-CDD4-4756-8372-51FAB8E97B13

P2860

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

http://www.wikidata.org/entity/Q34299534

description

2012 nî lūn-bûn

@nan

2012 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

@ast

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

@en

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

@nl

type

label

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

@ast

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

@en

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

@nl

prefLabel

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

@ast

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

@en

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

@nl

P1433

Q34299534-5931AD69-BB1D-47DF-81FE-6399A96DAE05

P1476

Q34299534-D6498B7E-F3E9-4FA3-8377-10DEC32B948B

P2093

Q34299534-15A315F8-4C78-45C7-B9CE-0637A7F8F15F

Q34299534-2562E989-6EE2-4CD8-A3B9-34B2C7CC1639

Q34299534-2DC18166-F654-4048-AB2A-EE1CFC716A1E

Q34299534-535F9347-DC5D-4013-90F5-A68DE33533D7

Q34299534-5E603346-E7E6-43D0-B5ED-5634818424E4

Q34299534-68ACF031-B7D9-4C19-9CE9-02A34C6AB0E6

Q34299534-9813D9EA-FF47-4802-B460-2F6D98D8F0EE

Q34299534-F13B6D5A-3940-4643-8817-AFAEE574FC07

Q34299534-FA7B1C0F-13C0-4087-BAD0-E00A0C8802DB

P2860

Q34299534-0200A6F2-E6A6-4AD3-A0A2-6C3F094D254F

Q34299534-05C03C58-E3D3-446D-97F7-B7FDA117C797

Q34299534-06C9586B-E7FC-46D6-B4A3-832B8F5A6FB6

Q34299534-085AB2DD-5190-48B6-AA8B-3FBCD4C06AA1

Q34299534-098627FE-25C3-48A5-BA58-0E97EE281EFB

Q34299534-098EF94A-66C2-421C-BC78-00078B2DCB9E

Q34299534-0CC87B73-22C4-4E3D-A6CC-1DCC851DA5B2

Q34299534-0E06D43A-2328-41DE-8CC8-4C7AE29A23F1

Q34299534-11F0CBD3-F5A7-423B-8533-403F80FC0F2E

Q34299534-143F8C7F-F45C-40F3-9DF7-F7EA825C9DB0

P304

Q34299534-08E9ED8E-9962-4AA8-BC83-608326B9648D

P31

Q34299534-BAB54F76-5218-4FC5-BA47-64033C08D136

P356

Q34299534-6CA542A1-F6C8-4798-B860-BEA69E2BE1F8

P407

Q34299534-508C9C81-CBA6-4FA4-ACC6-0B36E0CDC8E7

P433

Q34299534-B6562104-8D5D-4DB6-997B-F0EEE7313755

P478

Q34299534-0D940114-491F-459A-BC82-294F820B7E66

P577

Q34299534-B2B4EE0D-4483-4D3A-8BC8-8C972E936899

P5875

Q34299534-9952D7FF-A443-40A3-A93E-E7E00A1BC896

P698

Q34299534-DB910934-B253-4974-B966-A4767FAB479D

P921

Q34299534-E14E0C23-3834-4674-9593-2D506415A57D

P932

Q34299534-43C717E2-50D8-4D9B-A93A-3BC623D2D294

P356

JOURNAL.PONE.0037366

P1433

P1476

microRNA-21 governs TORC1 activation in renal cancer cell proliferation and invasion

@en

P2093

Balakuntalam S Kasinath

http://www.w3.org/2001/XMLSchema#string

Chandi Charan Mandal

http://www.w3.org/2001/XMLSchema#string

Dipen J Parekh

http://www.w3.org/2001/XMLSchema#string

Falguni Das

http://www.w3.org/2001/XMLSchema#string

Goutam Ghosh Choudhury

http://www.w3.org/2001/XMLSchema#string

Hanna E Abboud

http://www.w3.org/2001/XMLSchema#string

Karen Block

http://www.w3.org/2001/XMLSchema#string

Nandini Ghosh-Choudhury

http://www.w3.org/2001/XMLSchema#string

Nirmalya Dey

http://www.w3.org/2001/XMLSchema#string

P2860

Hallmarks of Cancer: The Next Generation

Activation of mTORC2 by association with the ribosome

Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex

Rictor, a novel binding partner of mTOR, defines a rapamycin-insensitive and raptor-independent pathway that regulates the cytoskeleton

Raptor, a binding partner of target of rapamycin (TOR), mediates TOR action

Mammalian TOR complex 2 controls the actin cytoskeleton and is rapamycin insensitive

Two TOR complexes, only one of which is rapamycin sensitive, have distinct roles in cell growth control

The tumor suppressor, PTEN/MMAC1, dephosphorylates the lipid second messenger, phosphatidylinositol 3,4,5-trisphosphate

Inhibition of cell migration, spreading, and focal adhesions by tumor suppressor PTEN

MicroRNAs: target recognition and regulatory functions

P304

e37366

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1371/JOURNAL.PONE.0037366

http://www.w3.org/2001/XMLSchema#string

P407

P433

6

http://www.w3.org/2001/XMLSchema#string

P478

7

http://www.w3.org/2001/XMLSchema#string

P577

2012-06-04T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

225287758

http://www.w3.org/2001/XMLSchema#string

P698

22685542

http://www.w3.org/2001/XMLSchema#string

P921

P932

3368259

http://www.w3.org/2001/XMLSchema#string