Epidermal growth factor receptor expression escapes androgen regulation in prostate cancer: a potential molecular switch for tumour growth.
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The dark side of 5α-reductase inhibitors' therapy: sexual dysfunction, high Gleason grade prostate cancer and depressionPersistent androgen receptor addiction in castration-resistant prostate cancerCombined inhibition of epidermal growth factor receptor and cyclooxygenase-2 leads to greater anti-tumor activity of docetaxel in advanced prostate cancerRegulation of PSMB5 protein and β subunits of mammalian proteasome by constitutively activated signal transducer and activator of transcription 3 (STAT3): potential role in bortezomib-mediated anticancer therapy.Loss of EGFR signaling regulated miR-203 promotes prostate cancer bone metastasis and tyrosine kinase inhibitors resistance.Revisiting the role of antiandrogen strategies in ovarian cancer.BZL101, a phytochemical extract from the Scutellaria barbata plant, disrupts proliferation of human breast and prostate cancer cells through distinct mechanisms dependent on the cancer cell phenotype.Genistein up-regulates tumor suppressor microRNA-574-3p in prostate cancer.Difference in protein expression profile and chemotherapy drugs response of different progression stages of LNCaP sublines and other human prostate cancer cellsAndrogen receptor signaling in prostate cancer development and progression.Emerging targeted therapies for castration-resistant prostate cancer.Paxillin mediates extranuclear and intranuclear signaling in prostate cancer proliferation.Nuclear Kaiso indicates aggressive prostate cancers and promotes migration and invasiveness of prostate cancer cells.EGF Receptor Promotes Prostate Cancer Bone Metastasis by Downregulating miR-1 and Activating TWIST1.Oncogenic EGFR Represses the TET1 DNA Demethylase to Induce Silencing of Tumor Suppressors in Cancer Cells.Co-targeting EGFR and survivin with a bivalent aptamer-dual siRNA chimera effectively suppresses prostate cancerThe osteoblastic and osteoclastic interactions in spinal metastases secondary to prostate cancer.AR-Signaling in Human Malignancies: Prostate Cancer and Beyond.Gαs protein expression is an independent predictor of recurrence in prostate cancerNeoadjuvant therapy for localized prostate cancer: Examining mechanism of action and efficacy within the tumor.Targeting the relaxin hormonal pathway in prostate cancer.Adverse effects of 5α-reductase inhibitors: What do we know, don't know, and need to know?HER2 and EGFR Overexpression Support Metastatic Progression of Prostate Cancer to Bone.Notch Pathway Inhibition Using PF-03084014, a γ-Secretase Inhibitor (GSI), Enhances the Antitumor Effect of Docetaxel in Prostate Cancer.Screening and biological evaluation of myricetin as a multiple target inhibitor insulin, epidermal growth factor, and androgen receptor; in silico and in vitro.Hsp27 regulates EGF/β-catenin mediated epithelial to mesenchymal transition in prostate cancer.EGFR mediates docetaxel resistance in human castration-resistant prostate cancer through the Akt-dependent expression of ABCB1 (MDR1).Influence of peripheral whole-blood microRNA-7 and microRNA-221 high expression levels on the acquisition of castration-resistant prostate cancer: evidences from in vitro and in vivo studies.Investigational serine/threonine kinase inhibitors against prostate cancer metastases.Randomized Phase II trial of nintedanib, afatinib and sequential combination in castration-resistant prostate cancer.SPRY2 loss enhances ErbB trafficking and PI3K/AKT signalling to drive human and mouse prostate carcinogenesisMiR-146a suppresses tumor growth and progression by targeting EGFR pathway and in a p-ERK-dependent manner in castration-resistant prostate cancer.Loss of EGFR induced autophagy sensitizes hormone refractory prostate cancer cells to adriamycin.Androgen receptor expression on circulating tumor cells in metastatic breast cancer.Immunohistochemical expression of PDGFR, VEGF-C, and proteins of the mToR pathway before and after androgen deprivation therapy in prostate carcinoma: significant decrease after treatment.Combination of Carmustine and Selenite Inhibits EGFR Mediated Growth Signaling in Androgen-Independent Prostate Cancer Cells.Disruption of ETV6 leads to TWIST1-dependent progression and resistance to epidermal growth factor receptor tyrosine kinase inhibitors in prostate cancer.Multigene profiling of CTCs in mCRPC identifies a clinically relevant prognostic signature.Decline in Arylsulfatase B Expression Increases EGFR Expression by Inhibiting the Protein Tyrosine Phosphatase SHP2 and Activating JNK in Prostate Cells.Restoration of microRNA-130b expression suppresses osteosarcoma cell malignant behavior in vitro.
P2860
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P2860
Epidermal growth factor receptor expression escapes androgen regulation in prostate cancer: a potential molecular switch for tumour growth.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh
2009年學術文章
@zh-hant
name
Epidermal growth factor recept ...... ular switch for tumour growth.
@en
Epidermal growth factor recept ...... ular switch for tumour growth.
@nl
type
label
Epidermal growth factor recept ...... ular switch for tumour growth.
@en
Epidermal growth factor recept ...... ular switch for tumour growth.
@nl
prefLabel
Epidermal growth factor recept ...... ular switch for tumour growth.
@en
Epidermal growth factor recept ...... ular switch for tumour growth.
@nl
P2860
P921
P356
P1476
Epidermal growth factor recept ...... ular switch for tumour growth.
@en
P2093
A M Traish
A Morgentaler
P2860
P2888
P304
P356
10.1038/SJ.BJC.6605376
P407
P577
2009-11-03T00:00:00Z
2009-12-15T00:00:00Z
P5875
P6179
1003897368