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Image Search Results
Journal: Journal of Clinical Medicine
Article Title: Thrombin Preconditioning of Extracellular Vesicles Derived from Mesenchymal Stem Cells Accelerates Cutaneous Wound Healing by Boosting Their Biogenesis and Enriching Cargo Content
doi: 10.3390/jcm8040533
Figure Lengend Snippet: The EVs contain various cytokines and chemokines following stimulation with different wound mimetic environments. EVs were isolated from MSCs preconditioned with thrombin (40 U), LPS (1 μg,) H 2 O 2 (50 μM), or hypoxia (O 2 10%). ( A ) Representative screening X-ray film blot of Proteome Profiler Human Angiogenesis Array (PPHAA) for protein cargos of EVs (upper panel) and their representative diagram for the relative content of each protein expressed by fold change of blot intensity normalized with that of the naïve group. A gray dot line represents a three-fold increase over that of the naïve group. ( B ) Levels of angiogenin, angiopoietin-1, VEGF, and HGF measured by muliplex ELISA in EVs. Statistical analyses were carried out using a One-way Analysis of Variance (ANOVA). The asterisk (*) indicates p < 0.05 compared with naive EVs, the number sign (#) indicates p < 0.05 compared with the 10% oxygen-treated EV group, the double dagger (‡) indicates p < 0.05 compared to the H 2 O 2 -treated EV group, and the dollar sign ($) indicates p < 0.05 compared with the LPS-treated EV group ( n = 5 per each analysis).
Article Snippet: The relative expression of 55 angiogenesis-related proteins was determined in each lysate using a
Techniques: Isolation, Enzyme-linked Immunosorbent Assay
Journal: Oncotarget
Article Title: PTEN mediates the cross talk between breast and glial cells in brain metastases leading to rapid disease progression.
doi: 10.18632/oncotarget.14047
Figure Lengend Snippet: Figure 7: Effects of glial cell cocultures on cytokine secretion. Control and PTEN overexpressing MDA-MB-231 BR cells were seeded in transwell inserts and cocultured for 48 h with astrocytes (A) or microglia (B). Antibody-spotted membranes were incubated with conditioned media of these cultures and levels of secreted proteins were visualized by HRP-conjugated antibodies. Proteins with a more than 2-fold expression difference are shown by open boxes. Results were verified by qPCR analyses (C). Astrocyte coculture reduced EGF and GM-CSF expression significantly in PTEN overexpressing (PTEN CoA) compared to control cells (CTL CoA, C). Astrocytes express the GM- CSF receptor (CSFR2A) only when cocultured with tumor cells. Microglia coculture reduced VEGFA expression in PTEN overexpressing (PTEN CoMG) compared to control cells (CTL CoMG). Student’s t-test was used to analyze statistical significance. *p < 0.05.
Article Snippet: Cytokine secretion was estimated from CM by Proteome ProfilerTM Antibody Array (
Techniques: Control, Incubation, Expressing
Journal: Cancers
Article Title: Visfatin Mediates Malignant Behaviors through Adipose-Derived Stem Cells Intermediary in Breast Cancer
doi: 10.3390/cancers12010029
Figure Lengend Snippet: GDF15 play a crucial role in the regulations of breast cancer cells activities by visfatin-treated ADSCs (vADSCs). ( A ) After the three-day co-culture of MDA-MB-231 cells and vADSCs (V50 and V100 group) or untreated ADSCs (Ctrl group), the CM was collected and analyzed by using a cytokine array kit. ( B ) The expression of GDF15 in the co-cultured CM was validated by ELISA represented in a histogram. The ADSCs and MDA-MB-231 cells collected from the co-culture system were extracted for cell lysate to analyze the GDF15 expression by western blotting. ( C ) The migration and invasion of MDA-MB-231 treated with GDF15 at various concentrations for 48 h were evaluated by using a transwell system. ( D ) The indirect co-culture was performed in the presence or absence of the GDF15 neutralizing antibody of for three days. After that, the migration and invasion of the MDA-MB-231 cells collected from the co-culture were evaluated in a transwell system. ( E ) The expression of phosphor-AKT (pAKT) of MDA-MB-231 treated with GDF15 (50 ng/mL) at different time point was detected by western blotting. ( F ) The pAKT was detected in the MDA-MB-231 cells from the co-culture by western blotting. ( G ) After the three-day co-culture in the presence or absence of the wortmannin (400 nM), the MDA-MB-231 cells were collected from the co-culture for performing the migration assay. All experiments were performed in triplicate.
Article Snippet: To explore the cytokine expression profile in the medium of the indirect co-culture of MDA-MB-231 and resistin-pretreated ADSCs, a
Techniques: Co-Culture Assay, Expressing, Cell Culture, Enzyme-linked Immunosorbent Assay, Western Blot, Migration
Journal: International Journal of Molecular Sciences
Article Title: Insight into Cisplatin-Resistance Signaling of W1 Ovarian Cancer Cells Emerges mTOR and HSP27 as Targets for Sensitization Strategies
doi: 10.3390/ijms21239240
Figure Lengend Snippet: ( a ) Data set of a human proteome profiler kinase activity array displaying the phosphorylated/activated form of the components in cisplatin (cDDP)-treated W1 and W1CR cells with and without collagen ( n = 1). ( b ) Overview of the investigated signaling pathway and inhibitory approaches.
Article Snippet: A
Techniques: Activity Assay
Journal: OncoTargets and therapy
Article Title: Overexpression of ETV4 protein in triple-negative breast cancer is associated with a higher risk of distant metastasis
doi: 10.2147/OTT.S66692
Figure Lengend Snippet: Relative expression comparison for 84 metastasis-related genes between triple-negative breast cancer (TNBC) and luminal A breast cancer tissue detected using a Human Tumor Metastasis RT 2 Profiler™ PCR Array. Notes: The figure depicts a log transformation plot of the relative expression level of each gene (ΔΔCt) between TNBC (y-axis) and luminal A (x-axis). The red lines indicate a three-fold change in gene expression threshold. Abbreviations: PCR, polymerase chain reaction; ETV4, ETS translocation variant 4; MMP, matrix metalloproteinase.
Article Snippet: Real-time PCR was then performed on each sample using the
Techniques: Expressing, Comparison, Transformation Assay, Gene Expression, Polymerase Chain Reaction, Translocation Assay, Variant Assay