The extracellular matrix protein TGFBI induces microtubule stabilization and sensitizes ovarian cancers to paclitaxel
about
SIK2 is a centrosome kinase required for bipolar mitotic spindle formation that provides a potential target for therapy in ovarian cancerRethinking ovarian cancer II: reducing mortality from high-grade serous ovarian cancerMitotic Spindle Disruption by Alternating Electric Fields Leads to Improper Chromosome Segregation and Mitotic Catastrophe in Cancer Cells.Stroma-associated master regulators of molecular subtypes predict patient prognosis in ovarian cancer.miR-337-3p and its targets STAT3 and RAP1A modulate taxane sensitivity in non-small cell lung cancersA time- and matrix-dependent TGFBR3-JUND-KRT5 regulatory circuit in single breast epithelial cells and basal-like premalignanciesSuppression of annexin A11 in ovarian cancer: implications in chemoresistance.Tumor suppressor protein DAB2IP participates in chromosomal stability maintenance through activating spindle assembly checkpoint and stabilizing kinetochore-microtubule attachments.ProbFAST: Probabilistic functional analysis system tool.Loss of PFKFB4 induces cell death in mitotically arrested ovarian cancer cellsActivation of YAP1 is associated with poor prognosis and response to taxanes in ovarian cancer.Consistent metagenes from cancer expression profiles yield agent specific predictors of chemotherapy response.RNA interference (RNAi) screening approach identifies agents that enhance paclitaxel activity in breast cancer cells.Limitations in Adjuvant Breast Cancer Therapy: The Predictive Potential of Pharmacogenetics and Pharmacogenomics.Genomic analysis of genetic heterogeneity and evolution in high-grade serous ovarian carcinoma.The role of TGFBI in mesothelioma and breast cancer: association with tumor suppression.Systems analysis of a mouse xenograft model reveals annexin A1 as a regulator of gene expression in tumor stroma.Discoidin domain receptor 1 contributes to tumorigenesis through modulation of TGFBI expression.MicroRNA-mediated regulation of extracellular matrix formation modulates somatic cell reprogrammingMiR-21 plays an important role in radiation induced carcinogenesis in BALB/c mice by directly targeting the tumor suppressor gene Big-h3.Gallotannin imposes S phase arrest in breast cancer cells and suppresses the growth of triple-negative tumors in vivo.TGFBI expression reduces in vitro and in vivo metastatic potential of lung and breast tumor cells.Src family kinases and paclitaxel sensitivity.A genistein derivative, ITB-301, induces microtubule depolymerization and mitotic arrest in multidrug-resistant ovarian cancer.Lysosomal trafficking of TGFBIp via caveolae-mediated endocytosis.Up-regulation of miR-877 induced by paclitaxel inhibits hepatocellular carcinoma cell proliferation though targeting FOXM1.Proteomic identification of betaig-h3 as a lysophosphatidic acid-induced secreted protein of human mesenchymal stem cells: paracrine activation of A549 lung adenocarcinoma cells by betaig-h3.TGFBI promoter hypermethylation correlating with paclitaxel chemoresistance in ovarian cancer.Bioinformatics Analyses of the Role of Vascular Endothelial Growth Factor in Patients with Non-Small Cell Lung CancerReversal of Chemoresistance in Ovarian Cancer by Co-Delivery of a P-Glycoprotein Inhibitor and Paclitaxel in a Liposomal Platform.SPARC Regulates Transforming Growth Factor Beta Induced (TGFBI) Extracellular Matrix Deposition and Paclitaxel Response in Ovarian Cancer Cells.Transforming growth Factor-Beta-Induced Protein (TGFBI)/(βig-H3): a matrix protein with dual functions in ovarian cancer.ß3 integrin modulates transforming growth factor beta induced (TGFBI) function and paclitaxel response in ovarian cancer cells.Release of TGFβig-h3 by gastric myofibroblasts slows tumor growth and is decreased with cancer progression.Expression and correlation of Lewis y antigen and TGF-β1 in ovarian epithelial carcinoma.Identification of heterogeneity among soft tissue sarcomas by gene expression profiles from different tumorsTubulin-targeting agent combination therapies: dosing schedule could matter.Altered protein conformation and lower stability of the dystrophic transforming growth factor beta-induced protein mutants.Constitutive Cdk2 activity promotes aneuploidy while altering the spindle assembly and tetraploidy checkpoints.Modulating microtubule stability enhances the cytotoxic response of cancer cells to Paclitaxel
P2860
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P2860
The extracellular matrix protein TGFBI induces microtubule stabilization and sensitizes ovarian cancers to paclitaxel
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh
2007年學術文章
@zh-hant
name
The extracellular matrix prote ...... ovarian cancers to paclitaxel
@ast
The extracellular matrix prote ...... ovarian cancers to paclitaxel
@en
type
label
The extracellular matrix prote ...... ovarian cancers to paclitaxel
@ast
The extracellular matrix prote ...... ovarian cancers to paclitaxel
@en
prefLabel
The extracellular matrix prote ...... ovarian cancers to paclitaxel
@ast
The extracellular matrix prote ...... ovarian cancers to paclitaxel
@en
P2093
P2860
P50
P1433
P1476
The extracellular matrix prote ...... ovarian cancers to paclitaxel
@en
P2093
Adam McGeoch
Ahmed Ashour Ahmed
Anthony D Mills
Ashraf E K Ibrahim
Barbara Nicke
Jillian Temple
Maria Vias
Robin Crawford
Ronald A Laskey
P2860
P304
P356
10.1016/J.CCR.2007.11.014
P50
P577
2007-12-01T00:00:00Z