FOXM1 is a transcriptional target of ERalpha and has a critical role in breast cancer endocrine sensitivity and resistance - Wikidata - wikimedia - TriplyDB

FOXM1 is a transcriptional target of ERalpha and has a critical role in breast cancer endocrine sensitivity and resistance

FOXM1 is a transcriptional target of ERalpha and has a critical role in breast cancer endocrine sensitivity and resistance

http://www.wikidata.org/entity/Q33869864

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The Role of Forkhead Box Protein M1 in Breast Cancer Progression and Resistance to Therapy Exploiting FOXM1-orchestrated molecular network for early squamous cell carcinoma diagnosis and prognosis 3, 3'-Diindolylmethane enhances the effectiveness of herceptin against HER-2/neu-expressing breast cancer cells Integrative analysis of miRNA and gene expression reveals regulatory networks in tamoxifen-resistant breast cancer GSAASeqSP: a toolset for gene set association analysis of RNA-Seq data Glyceollins trigger anti-proliferative effects through estradiol-dependent and independent pathways in breast cancer cells Estrogen receptor coregulators and pioneer factors: the orchestrators of mammary gland cell fate and development.FoxM1 is associated with poor prognosis of non-small cell lung cancer patients through promoting tumor metastasis.Mammary glands exhibit molecular laterality and undergo left-right asymmetric ductal epithelial growth in MMTV-cNeu mice.Resistance to HER2-targeted therapies: a potential role for FOXM1.Targeting of mutant p53-induced FoxM1 with thiostrepton induces cytotoxicity and enhances carboplatin sensitivity in cancer cells Multiple faces of FoxM1 transcription factor: lessons from transgenic mouse models.Activating CAR and β-catenin induces uncontrolled liver growth and tumorigenesis.ERβ1 represses FOXM1 expression through targeting ERα to control cell proliferation in breast cancer.Increased expression of forkhead box M1 is associated with aggressive phenotype and poor prognosis in estrogen receptor-positive breast cancer.The suppression of FOXM1 and its targets in breast cancer xenograft tumors by siRNA Centromere protein-A, an essential centromere protein, is a prognostic marker for relapse in estrogen receptor-positive breast cancer Forkhead box protein M1 predicts outcome in human osteosarcoma miR-204 inhibits invasion and epithelial-mesenchymal transition by targeting FOXM1 in esophageal cancer.Forkhead box M1 is regulated by heat shock factor 1 and promotes glioma cells survival under heat shock stress Derailed estrogen signaling and breast cancer: an authentic couple.Estrogen receptors and human disease: an update.FoxM1 inhibition sensitizes resistant glioblastoma cells to temozolomide by downregulating the expression of DNA-repair gene Rad51.ATM and p53 regulate FOXM1 expression via E2F in breast cancer epirubicin treatment and resistance Genome-wide mapping of FOXM1 binding reveals co-binding with estrogen receptor alpha in breast cancer cells.Transcription factor interactions mediate EGF-dependent COX-2 expression.Crosstalk between PKCα and Notch-4 in endocrine-resistant breast cancer cells.OTUB1-catalyzed deubiquitination of FOXM1 facilitates tumor progression and predicts a poor prognosis in ovarian cancer.The Forkhead Box M1 protein regulates BRIP1 expression and DNA damage repair in epirubicin treatment.FOXK1 interaction with FHL2 promotes proliferation, invasion and metastasis in colorectal cancer.FOXM1 confers resistance to gefitinib in lung adenocarcinoma via a MET/AKT-dependent positive feedback loop.ErbB2, FoxM1 and 14-3-3ζ prime breast cancer cells for invasion in response to ionizing radiation.FOXM1 targets NBS1 to regulate DNA damage-induced senescence and epirubicin resistance FOXM1 and its oncogenic signaling in pancreatic cancer pathogenesis Role of the forkhead transcription factor FOXO-FOXM1 axis in cancer and drug resistance.FOX(M1) news--it is cancer.Role and regulation of the forkhead transcription factors FOXO3a and FOXM1 in carcinogenesis and drug resistance.Dissecting the genomic activity of a transcriptional regulator by the integrative analysis of omics data.InFlo: a novel systems biology framework identifies cAMP-CREB1 axis as a key modulator of platinum resistance in ovarian cancer.Selective estrogen receptor modulators and betulinic acid act synergistically to target ERα and SP1 transcription factor dependent Pygopus expression in breast cancer.

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FOXM1 is a transcriptional target of ERalpha and has a critical role in breast cancer endocrine sensitivity and resistance

http://www.wikidata.org/entity/Q33869864

description

2010 nî lūn-bûn

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2010 թուականի Մարտին հրատարակուած գիտական յօդուած

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2010 թվականի մարտին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年论文

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FOXM1 is a transcriptional tar ...... ine sensitivity and resistance

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FOXM1 is a transcriptional tar ...... ine sensitivity and resistance

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FOXM1 is a transcriptional tar ...... ine sensitivity and resistance

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FOXM1 is a transcriptional tar ...... ine sensitivity and resistance

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FOXM1 is a transcriptional tar ...... ine sensitivity and resistance

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FOXM1 is a transcriptional tar ...... ine sensitivity and resistance

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A E Lykkesfeldt

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A V Stavropoulou

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D Constantinidou

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J M-M Kwok

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J Millour

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K Sivanandan

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R C Coombes

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P2860

PD 0332991, a selective cyclin D kinase 4/6 inhibitor, preferentially inhibits proliferation of luminal estrogen receptor-positive human breast cancer cell lines in vitro

The Forkhead box M1 protein regulates the transcription of the estrogen receptor alpha in breast cancer cells

Regulation of the transcription factor FOXM1c by Cyclin E/CDK2

The human TRIDENT/HFH-11/FKHL16 gene: structure, localization, and promoter characterization

Chromosome-wide mapping of estrogen receptor binding reveals long-range regulation requiring the forkhead protein FoxA1

FoxM1 is degraded at mitotic exit in a Cdh1-dependent manner

FoxM1 is required for execution of the mitotic programme and chromosome stability

Forkhead box M1B transcriptional activity requires binding of Cdk-cyclin complexes for phosphorylation-dependent recruitment of p300/CBP coactivators

New colorimetric cytotoxicity assay for anticancer-drug screening

Identification and validation of commonly overexpressed genes in solid tumors by comparison of microarray data.

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20208560

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