Reduced PTEN expression predicts relapse in patients with breast carcinoma treated by tamoxifen.
about
Treating breast cancer through novel inhibitors of the phosphatidylinositol 3'-kinase pathway.Phosphatidylinositol 3-kinase and antiestrogen resistance in breast cancerRegulation of mammary stem/progenitor cells by PTEN/Akt/beta-catenin signalingPathways to tamoxifen resistance.Luminal breast cancer cell lines overexpressing ZNF703 are resistant to tamoxifen through activation of Akt/mTOR signalingPIK3CA and PIK3CB inhibition produce synthetic lethality when combined with estrogen deprivation in estrogen receptor-positive breast cancer.Clinical potential of novel therapeutic targets in breast cancer: CDK4/6, Src, JAK/STAT, PARP, HDAC, and PI3K/AKT/mTOR pathways.PTEN and p53 cross-regulation induced by soy isoflavone genistein promotes mammary epithelial cell cycle arrest and lobuloalveolar differentiationGlobal characterization of signalling networks associated with tamoxifen resistance in breast cancer.Overcoming endocrine resistance due to reduced PTEN levels in estrogen receptor-positive breast cancer by co-targeting mammalian target of rapamycin, protein kinase B, or mitogen-activated protein kinase kinase.Correlation between activation of PI3K/AKT/mTOR pathway and prognosis of breast cancer in Chinese women.Targeting PTEN-defined breast cancers with a one-two punch.Integrative Analysis of Response to Tamoxifen Treatment in ER-Positive Breast Cancer Using GWAS Information and Transcription ProfilingMutations in the phosphatidylinositol 3-kinase pathway: role in tumor progression and therapeutic implications in breast cancer.Partial PTEN deletion is linked to poor prognosis in breast cancerPreclinical and clinical studies of estrogen deprivation support the PDGF/Abl pathway as a novel therapeutic target for overcoming endocrine resistance in breast cancer.The impact of PTEN tumor suppressor gene on acquiring resistance to tamoxifen treatment in breast cancer patientsClinical trials update: endocrine and biological therapy combinations in the treatment of breast cancer.New and emerging treatments for estrogen receptor-positive breast cancer: focus on everolimus.Mechanisms of endocrine resistance in breast cancer.Effects of indomethacin on expression of PTEN tumour suppressor in human cancersPTEN mutation, methylation and expression in breast cancer patients.PTEN in brain tumors.mTOR signaling feedback modulates mammary epithelial differentiation and restrains invasion downstream of PTEN loss.Endocrine resistance in breast cancer: focus on the phosphatidylinositol 3-kinase/akt/mammalian target of rapamycin signaling pathway.Estradiol-induced regression in T47D:A18/PKCalpha tumors requires the estrogen receptor and interaction with the extracellular matrix.Interaction of E-cadherin and PTEN regulates morphogenesis and growth arrest in human mammary epithelial cells.Status of PI3K inhibition and biomarker development in cancer therapeutics.Establishment and antitumor effects of dasatinib and PKI-587 in BD-138T, a patient-derived muscle invasive bladder cancer preclinical platform with concomitant EGFR amplification and PTEN deletion.Research on drug resistance mechanism of trastuzumab caused by activation of the PI3K/Akt signaling pathway.Intrinsic resistance to chemotherapy in breast cancer.Epigenetic modulation: a novel therapeutic target for overcoming hormonal therapy resistance.Everolimus: targeted therapy on the horizon for the treatment of breast cancer.PI3K in cancer-stroma interactions: bad in seed and ugly in soil.The proteasome inhibitor Bortezomib (Velcade) as potential inhibitor of estrogen receptor-positive breast cancer.The PI3K Pathway: Background and Treatment Approaches.Everolimus and its role in hormone-resistant and trastuzumab-resistant metastatic breast cancer.Akt-induced endocrine therapy resistance is reversed by inhibition of mTOR signaling.Insulin growth factor receptor-1 expression and loss of PTEN protein predict early recurrence in triple-negative breast cancer.A Potential Prognostic Long Noncoding RNA Signature to Predict Recurrence among ER-positive Breast Cancer Patients Treated with Tamoxifen.
P2860
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P2860
Reduced PTEN expression predicts relapse in patients with breast carcinoma treated by tamoxifen.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
Reduced PTEN expression predic ...... arcinoma treated by tamoxifen.
@en
Reduced PTEN expression predic ...... arcinoma treated by tamoxifen.
@nl
type
label
Reduced PTEN expression predic ...... arcinoma treated by tamoxifen.
@en
Reduced PTEN expression predic ...... arcinoma treated by tamoxifen.
@nl
prefLabel
Reduced PTEN expression predic ...... arcinoma treated by tamoxifen.
@en
Reduced PTEN expression predic ...... arcinoma treated by tamoxifen.
@nl
P2093
P2860
P1433
P1476
Reduced PTEN expression predic ...... arcinoma treated by tamoxifen.
@en
P2093
Andrew McFadden
Emina Torlakovic
Miķelis G Bickis
Nael Shoman
Rajni Chibbar
Shannon Klassen
P2860
P2888
P304
P356
10.1038/MODPATHOL.3800296
P577
2005-02-01T00:00:00Z
P6179
1028631783