Interactions with fibroblasts are distinct in Basal-like and luminal breast cancers.
about
Tumor angiogenesis: pericytes and maturation are not to be ignoredDirect Interaction between Carcinoma Cells and Cancer Associated Fibroblasts for the Regulation of Cancer InvasionInsights into Orphan Nuclear Receptors as Prognostic Markers and Novel Therapeutic Targets for Breast CancerInteractions between tumor cells and microenvironment in breast cancer: a new opportunity for targeted therapyRelationship of mammographic density and gene expression: analysis of normal breast tissue surrounding breast cancer.Weight Loss Reversed Obesity-Induced HGF/c-Met Pathway and Basal-Like Breast Cancer ProgressionCabozantinib (XL184) Inhibits Growth and Invasion of Preclinical TNBC Models.Distinctive responsiveness to stromal signaling accompanies histologic grade programming of cancer cellsSystematic bias in genomic classification due to contaminating non-neoplastic tissue in breast tumor samples.Differential gene expression between African American and European American colorectal cancer patients.Malignant stroma increases luminal breast cancer cell proliferation and angiogenesis through platelet-derived growth factor signalingProbing biological nanotopology via diffusion of weakly constrained plasmonic nanorods with optical coherence tomographyObesity-mediated regulation of HGF/c-Met is associated with reduced basal-like breast cancer latency in parous mice.Longitudinal study of mammary epithelial and fibroblast co-cultures using optical coherence tomography reveals morphological hallmarks of pre-malignancy.Parity-related molecular signatures and breast cancer subtypes by estrogen receptor statusThymic stromal lymphopoietin fosters human breast tumor growth by promoting type 2 inflammationBenign breast tissue composition in breast cancer patients: association with risk factors, clinical variables, and gene expressionSystematic assessment of prognostic gene signatures for breast cancer shows distinct influence of time and ER status.Interactions among genes, tumor biology and the environment in cancer health disparities: examining the evidence on a national and global scaleBreast cancer subtype-specific interactions with the microenvironment dictate mechanisms of invasion.Choosing the right cell line for breast cancer researchGene expression analysis of in vitro cocultures to study interactions between breast epithelium and stroma.Tumor intrinsic subtype is reflected in cancer-adjacent tissue.Fibroblasts Influence Survival and Therapeutic Response in a 3D Co-Culture ModelExtensive rewiring of epithelial-stromal co-expression networks in breast cancerCharacteristic Gene Expression Profiles of Human Fibroblasts and Breast Cancer Cells in a Newly Developed Bilateral Coculture SystemThe HSP90 Inhibitor Ganetespib Radiosensitizes Human Lung Adenocarcinoma Cells.Basal breast cancer: a complex and deadly molecular subtypeLaser Direct-Write Onto Live Tissues: A Novel Model for Studying Cancer Cell Migration.LIN28A Modulates Splicing and Gene Expression Programs in Breast Cancer Cells.Decreased Expression of TMEM173 Predicts Poor Prognosis in Patients with Hepatocellular CarcinomaGene expression in extratumoral microenvironment predicts clinical outcome in breast cancer patients.Analysis of terminal duct lobular unit involution in luminal A and basal breast cancers.Blood Genome-Wide Transcriptional Profiles of HER2 Negative Breast Cancers PatientsInverse-power-law behavior of cellular motility reveals stromal-epithelial cell interactions in 3D co-culture by OCT fluctuation spectroscopycMET inhibitor crizotinib impairs angiogenesis and reduces tumor burden in the C3(1)-Tag model of basal-like breast cancerBasal-like breast cancer cells induce phenotypic and genomic changes in macrophages.Imaging Extracellular Matrix Remodeling In Vitro by Diffusion-Sensitive Optical Coherence Tomography.Impact of tumor microenvironment and epithelial phenotypes on metabolism in breast cancerFibroblasts as architects of cancer pathogenesis
P2860
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P2860
Interactions with fibroblasts are distinct in Basal-like and luminal breast cancers.
description
2010 nî lūn-bûn
@nan
2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
name
Interactions with fibroblasts are distinct in Basal-like and luminal breast cancers.
@ast
Interactions with fibroblasts are distinct in Basal-like and luminal breast cancers.
@en
Interactions with fibroblasts are distinct in Basal-like and luminal breast cancers.
@nl
type
label
Interactions with fibroblasts are distinct in Basal-like and luminal breast cancers.
@ast
Interactions with fibroblasts are distinct in Basal-like and luminal breast cancers.
@en
Interactions with fibroblasts are distinct in Basal-like and luminal breast cancers.
@nl
prefLabel
Interactions with fibroblasts are distinct in Basal-like and luminal breast cancers.
@ast
Interactions with fibroblasts are distinct in Basal-like and luminal breast cancers.
@en
Interactions with fibroblasts are distinct in Basal-like and luminal breast cancers.
@nl
P2093
P2860
P1476
Interactions with fibroblasts are distinct in Basal-like and luminal breast cancers
@en
P2093
Delisha A Stewart
Erick Roman-Perez
Fathi Elloumi
J Terese Camp
Jessica Rein
Melissa A Troester
P2860
P356
10.1158/1541-7786.MCR-10-0372
P577
2010-12-03T00:00:00Z