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Cusabio
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Angio-Proteomie
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Boster Bio
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Boster Bio
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Becton Dickinson
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BioMimetic Therapeutics
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Merck KGaA
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GenScript corporation
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ReLIA Diagnostics
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Image Search Results
Journal: International Journal of General Medicine
Article Title: Effects of Sintilimab Plus Radiotherapy on Levels of Spondin-2 and Glucose Transporter-1 in Patients with Cervical Cancer
doi: 10.2147/IJGM.S461606
Figure Lengend Snippet: Levels of Serum Tumor Markers Before and After Six Cycles of Treatment ( \documentclass[12pt]{minimal} \usepackage{wasysym} \usepackage[substack]{amsmath} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage[mathscr]{eucal} \usepackage{mathrsfs} \DeclareFontFamily{T1}{linotext}{} \DeclareFontShape{T1}{linotext}{m}{n} {linotext }{} \DeclareSymbolFont{linotext}{T1}{linotext}{m}{n} \DeclareSymbolFontAlphabet{\mathLINOTEXT}{linotext} \begin{document} $\bar x\pm s$\end{document} )
Article Snippet: Then the levels of carcinoembryonic antigen (CEA), squamous cell carcinoma antigen (SCC-Ag), vascular endothelial growth factor-A (VEGF-A) and
Techniques: Control
Journal: Molecular medicine reports
Article Title: Antitumor activity of an adenovirus harboring two therapeutic genes, anti-VEGF ribozyme and human IL-24, in colon cancer.
doi: 10.3892/mmr_00000158
Figure Lengend Snippet: Figure 1. Schematic representation of the recombinant adenoviral vectors. An expression cassette containing (A) anti-VEGF ribozyme (Rz), (B) IL-24 and (C) anti-VEGF ribozyme + IL-24 (Rz/IL-24) was inserted into the deleted E1 region.
Article Snippet: The amplification conditions consisted of an initial 5-min denaturation step at 94 ̊C, followed by 50 cycles of 95 ̊C for 15 sec and 60 ̊C for 60 sec. To quantify the secreted VEGF protein in conditioned media from cells,
Techniques: Recombinant, Expressing
Journal: Molecular medicine reports
Article Title: Antitumor activity of an adenovirus harboring two therapeutic genes, anti-VEGF ribozyme and human IL-24, in colon cancer.
doi: 10.3892/mmr_00000158
Figure Lengend Snippet: Figure 2. Expression of anti-VEGF ribozyme RNA and IL-24 mRNA and protein in viral infected HT-29. A: (a) RT-PCR demonstrated that HT-29 cells did not express IL-24. Lane 1, marker; lane 2, cDNA from untreated HT-29 cells where no IL-24 expression was noted; lane 3, negative control, PCR for plasmid of pTrack-CMV-Rz; and lane 4, positive control, PCR for plasmid of pTrack-CMV-IL-24. A 621-bp DNA fragment was noted. (b) RT-PCR analysis of the expres sion of anti-VEGF ribozyme and IL-24 RNA in HT-29 cells. Lane 1, IL-24 in cells infected with Ad-IL-24; lane 2, anti-VEGF ribozyme with an expected length of 162 bp in cells infected with Ad-Rz; lane 3, marker; lane 4, IL-24 in cells infected with Ad-Rz/IL-24; and lane 5, anti-VEGF ribozyme in cells infected with Ad-Rz/IL-24 with an expected length of 214 bp. B: Results of immunofluorescence staining of IL-24 protein expression in cells treated with (c) PBS, (d) Ad-IL-24 and (e) Ad-Rz/IL-24. Left, light microscopy; right, fluorescence microscopy.
Article Snippet: The amplification conditions consisted of an initial 5-min denaturation step at 94 ̊C, followed by 50 cycles of 95 ̊C for 15 sec and 60 ̊C for 60 sec. To quantify the secreted VEGF protein in conditioned media from cells,
Techniques: Expressing, Infection, Reverse Transcription Polymerase Chain Reaction, Marker, Negative Control, Plasmid Preparation, Positive Control, Immunofluorescence, Staining, Light Microscopy, Fluorescence, Microscopy
Journal: Molecular medicine reports
Article Title: Antitumor activity of an adenovirus harboring two therapeutic genes, anti-VEGF ribozyme and human IL-24, in colon cancer.
doi: 10.3892/mmr_00000158
Figure Lengend Snippet: Figure 3. Cells treated with Ad-Rz/IL-24, Ad-IL-24 and Ad-Rz expressed reduced levels of VEGF. (A) Real-time PCR results, (B) ELISA results of VEGF protein secretion.
Article Snippet: The amplification conditions consisted of an initial 5-min denaturation step at 94 ̊C, followed by 50 cycles of 95 ̊C for 15 sec and 60 ̊C for 60 sec. To quantify the secreted VEGF protein in conditioned media from cells,
Techniques: Real-time Polymerase Chain Reaction, Enzyme-linked Immunosorbent Assay
Journal: Oncotarget
Article Title: γ-tocotrienol inhibits angiogenesis-dependent growth of human hepatocellular carcinoma through abrogation of AKT/mTOR pathway in an orthotopic mouse model
doi:
Figure Lengend Snippet: A, γ-tocotrienol inhibited HUVEC migration. An IBIDI culture insert (IBIDI GmbH) consists of two reservoirs separated by a 500 μm thick wall created by a culture insert in a 35mm petri dish. An equal number of HUVECs (70 μl; 5×10 5 cells/ml) were added into the two reservoirs of the same insert and incubated at 37°C/5% CO2. After 12 hours, the insert was gently removed creating a gap of ~500 μm. The cells were treated with 50 μM γ-tocotrienol for 12 h before being exposed to 10ng/mL VEGF for 24 h. Width of wound was measured at time zero and 24h of incubation with and without γ-tocotrienol. The representative photographs showed the same area at time zero and after 24 h of incubation. B, γ-tocotrienol inhibited HUVEC invasion through matrigel coated polycarbonate membrane. After pre-incubation with or without 50 μM γ-tocotrienol for 12 h, transwell chambers were then placed into the wells of a 24-well plate, in which we had added Medium 200 containing 10 ng/mL VEGF. After incubation for 24h cell invasion was analyzed and columns represent mean number of invaded cells. C, γ-Tocotrienol inhibited the VEGF-induced tube formation of endothelial cells in matrigel. After incubation, endothelial cells were fixed, and tubular structures were photographed (magnification, ×100). D, γ-Tocotrienol significantly inhibited the VEGF-induced cell survival of HUVECs. Cell viability was determined by MTT assay. *, p < 0.01 versus VEGF alone.
Article Snippet:
Techniques: Migration, Incubation, MTT Assay
Journal: Oncotarget
Article Title: γ-tocotrienol inhibits angiogenesis-dependent growth of human hepatocellular carcinoma through abrogation of AKT/mTOR pathway in an orthotopic mouse model
doi:
Figure Lengend Snippet: Aortic segments isolated from Sprague-Dawley rats were placed in the Matrigel coated plated and then overlayed with matrigel and treated with VEGF in the presence or absence of γ-tocotrienol. A, Representative photographs of sprouts from the margins of aortic rings. B, The number of sprouts were counted manually and epressed as a bar diagram. *, p < 0.01 versus VEGF alone.
Article Snippet:
Techniques: Isolation
Journal: Oncotarget
Article Title: γ-tocotrienol inhibits angiogenesis-dependent growth of human hepatocellular carcinoma through abrogation of AKT/mTOR pathway in an orthotopic mouse model
doi:
Figure Lengend Snippet: The rectangular filters papers contained VEGF alone or in combinaiton with γ-Tocotrienol. The representative photographs of control and γ-tocotrienol-treated CAMs were shown. B, The number of the microvessels was quantified manually and displayed as bar diagram *p < 0.01 versus VEGF alone. C, γ-Tocotrienol inhibits VEGF-induced angiogenesis in vivo . Six-week-old C57/BL/6 mice were injected with 0.5 mL of matrigel containing 10 or 20 μg γ-tocotrienol, 100 ng of VEGF, and 20 units of heparin into the ventral area (n = 5 per group). After 6 days, the skin of mice was pulled back to expose the intact Matrigel plugs and were photographed. D, γ-Tocotrienol inhibited blood vessel formation. The Matrigel plugs were fixed, sectioned, and stained with H&E (magnification, ×200).
Article Snippet:
Techniques: In Vivo, Injection, Staining
Journal: Oncotarget
Article Title: γ-tocotrienol inhibits angiogenesis-dependent growth of human hepatocellular carcinoma through abrogation of AKT/mTOR pathway in an orthotopic mouse model
doi:
Figure Lengend Snippet: A) Immunohistochemical analysis of Ki-67, VEGF, CD31, and cleaved caspase-3 showed the inhibition in expression of Ki-67, VEGF, and CD31 and increased levels of cleaved caspase-3 expression in γ-tocotrienol treated samples as compared with control group. Percentage indicates positive staining for the given biomarker. The photographs were taken at the magnification of 40 X. B) Western blot analysis of p-AKT, VEGF and cleaved caspase-3 proteins indicated a decrease in the expression of p-AKT and VEGF and increase in levels of cleaved caspase-3 expression in γ-tocotrienol treated samples as compared with control group. C) Effect of γ-tocotrienol on tumor-induced angiogenesis in-vivo . SCID mice were injected with 0.4 ml of Matrigel containing 5 × 10 6 single cell suspensions freshly derived from HCC patients (designated as HCC180811 and HCC 020113) and 20 units heparin with or without γ-tocotrienol (20 μg). Gross appearance of matrigel plugs retrieved from SCID mice 7 days post-injection were shown.
Article Snippet:
Techniques: Immunohistochemical staining, Inhibition, Expressing, Staining, Biomarker Assay, Western Blot, In Vivo, Injection, Derivative Assay