MicroRNA-200b targets protein kinase Cα and suppresses triple-negative breast cancer metastasis - Wikidata - awgldk - TriplyDB

MicroRNA-200b targets protein kinase Cα and suppresses triple-negative breast cancer metastasis

MicroRNA-200b targets protein kinase Cα and suppresses triple-negative breast cancer metastasis

http://www.wikidata.org/entity/Q34260220

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The miRacle in Pancreatic Cancer by miRNAs: Tiny Angels or Devils in Disease Progression MiRNAs and Other Epigenetic Changes as Biomarkers in Triple Negative Breast Cancer Functional Role of the microRNA-200 Family in Breast Morphogenesis and Neoplasia Human Cerberus prevents nodal-receptor binding, inhibits nodal signaling, and suppresses nodal-mediated phenotypes miR-200c Regulation of Metastases in Ovarian Cancer: Potential Role in Epithelial and Mesenchymal Transition The microRNA-200 family: small molecules with novel roles in cancer development, progression and therapy miR-30e-5p and miR-15a Synergistically Regulate Fatty Acid Metabolism in Goat Mammary Epithelial Cells via LRP6 and YAP1 High expression of cAMP-responsive element-binding protein 1 (CREB1) is associated with metastasis, tumor stage and poor outcome in gastric cancer.MiR130b-Regulation of PPARγ Coactivator- 1α Suppresses Fat Metabolism in Goat Mammary Epithelial Cells.Expression of miR-200c in claudin-low breast cancer alters stem cell functionality, enhances chemosensitivity and reduces metastatic potential.Dual regulation by microRNA-200b-3p and microRNA-200b-5p in the inhibition of epithelial-to-mesenchymal transition in triple-negative breast cancer MicroRNA-200 promotes lung cancer cell growth through FOG2-independent AKT activation.Modeling the Transitions between Collective and Solitary Migration Phenotypes in Cancer Metastasis.miR-34a Silences c-SRC to Attenuate Tumor Growth in Triple-Negative Breast Cancer.MiR-142-3p is a RANKL-dependent inducer of cell death in osteoclasts.MiR-940 Inhibited Cell Growth and Migration in Triple-Negative Breast Cancer MicroRNA-455-3p promotes invasion and migration in triple negative breast cancer by targeting tumor suppressor EI24.The role of microRNAs in metal carcinogen-induced cell malignant transformation and tumorigenesis.Long noncoding RNA PVT1 promotes cervical cancer progression through epigenetically silencing miR-200b.A negative feedback loop between miR-200b and the nuclear factor-κB pathway via IKBKB/IKK-β in breast cancer cells.MicroRNA-200b inhibits pituitary tumor cell proliferation and invasion by targeting PKCα Tumor suppressor role of microRNA-1296 in triple-negative breast cancer The microRNAs miR-200b-3p and miR-429-5p target the LIMK1/CFL1 pathway to inhibit growth and motility of breast cancer cells.Upregulation of histone-lysine methyltransferases plays a causal role in hexavalent chromium-induced cancer stem cell-like property and cell transformation.Mechanism of prolactin inhibition of miR-135b via methylation in goat mammary epithelial cells.Bioinformatics identification of dysregulated microRNAs in triple negative breast cancer based on microRNA expression profiling.miR-148a and miR-17-5p synergistically regulate milk TAG synthesis via PPARGC1A and PPARA in goat mammary epithelial cells.miR-200b-3p in plasma is a potential diagnostic biomarker in oral squamous cell carcinoma.Effect of miR-146a-5p on proliferation and metastasis of triple-negative breast cancer via regulation of SOX5.MicroRNA-150 suppresses triple-negative breast cancer metastasis through targeting HMGA2.Nanoparticle-Mediated Therapeutic Agent Delivery for Treating Metastatic Breast Cancer-Challenges and Opportunities.The Epigenetics of Triple-Negative and Basal-Like Breast Cancer: Current Knowledge MicroRNAs in regulation of triple-negative breast cancer progression

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P2860

MicroRNA-200b targets protein kinase Cα and suppresses triple-negative breast cancer metastasis

http://www.wikidata.org/entity/Q34260220

description

2014 nî lūn-bûn

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2014 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հունիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

MicroRNA-200b targets protein ...... ative breast cancer metastasis

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MicroRNA-200b targets protein ...... ative breast cancer metastasis

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MicroRNA-200b targets protein ...... ative breast cancer metastasis

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type

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MicroRNA-200b targets protein ...... ative breast cancer metastasis

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MicroRNA-200b targets protein ...... ative breast cancer metastasis

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MicroRNA-200b targets protein ...... ative breast cancer metastasis

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prefLabel

MicroRNA-200b targets protein ...... ative breast cancer metastasis

@ast

MicroRNA-200b targets protein ...... ative breast cancer metastasis

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MicroRNA-200b targets protein ...... ative breast cancer metastasis

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MicroRNA-200b targets protein ...... ative breast cancer metastasis

@en

P2093

Brock Humphries

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

Chengfeng Yang

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Dongfeng Tan

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

Theresa Fisher

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

Yuehua Cui

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

Zhishan Wang

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

P2860

miR-200 enhances mouse breast cancer cell colonization to form distant metastases

Hallmarks of Cancer: The Next Generation

Protein kinase C α is a central signaling node and therapeutic target for breast cancer stem cells

Clustering and conservation patterns of human microRNAs

The miR-200 family inhibits epithelial-mesenchymal transition and cancer cell migration by direct targeting of E-cadherin transcriptional repressors ZEB1 and ZEB2

The ZEB/miR-200 feedback loop--a motor of cellular plasticity in development and cancer?

The miR-200 family determines the epithelial phenotype of cancer cells by targeting the E-cadherin repressors ZEB1 and ZEB2

Contextual extracellular cues promote tumor cell EMT and metastasis by regulating miR-200 family expression

A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes

A reciprocal repression between ZEB1 and members of the miR-200 family promotes EMT and invasion in cancer cells

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10.1093/CARCIN/BGU133

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10

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35

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24925028

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4178468

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