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  <item rdf:about="https://ir.lib.ncu.edu.tw/handle/987654321/50866">
    <title>Transitional cell carcinoma of the ovary</title>
    <link>https://ir.lib.ncu.edu.tw/handle/987654321/50866</link>
    <description>title: Transitional cell carcinoma of the ovary</description>
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  <item rdf:about="https://ir.lib.ncu.edu.tw/handle/987654321/50863">
    <title>Topical application of marine briarane-type diterpenes effectively inhibits 12-O-tetradecanoylphorbol-13-acetate-induced inflammation and dermatitis in murine skin</title>
    <link>https://ir.lib.ncu.edu.tw/handle/987654321/50863</link>
    <description>title: Topical application of marine briarane-type diterpenes effectively inhibits 12-O-tetradecanoylphorbol-13-acetate-induced inflammation and dermatitis in murine skin abstract: Background: Skin is the largest organ in the body, and is directly exposed to extrinsic assaults. As such, the skin plays a central role in host defense and the cutaneous immune system is able to elicit specific local inflammatory and systemic immune responses against harmful stimuli. 12-O-tetradecanoylphorbol-13-acetate (TPA) can stimulate acute and chronic inflammation and tumor promotion in skin. TPA-induced dermatitis is thus a useful in vivo pharmacological platform for drug discovery. In this study, the inhibitory effect of briarane-type diterpenes (BrDs) from marine coral Briareum excavatum on TPA-induced dermatitis and dendritic cell (DC) function was explored. Methods: Evans blue dye exudation was used to determine vascular permeability. H&amp;E-stained skin section was used to determine the formation of edema in mouse abdominal skin. We also used immunohistochemistry staining and western blot assays to evaluate the activation of specific inflammation makers and key mediators of signaling pathway in the mouse skin. Furthermore, mouse bone marrow DCs were used to determine the relationship between the chemical structure of BrDs and their regulation of DC function. Results: BrD1 remarkably suppressed TPA-induced vascular permeability and edema in skin. At the biochemical level, BrD1 inhibited TPA-induced expression of cyclooxygenase-2, inducible nitric oxide synthase and matrix metalloproteinase-9, the key indicators of cutaneous inflammation. This inhibition was apparently mediated by interference with the Akt/NF-kappa B-mediated signaling network. BrD1 also inhibited TNF-alpha and IL-6 expression in LPS-stimulated BMDCs. The 8, 17-epoxide of BrDs played a crucial role in the inhibition of IL-6 expression, and replacement of the C-12 hydroxyl group with longer esters in BrDs gradually decreased this inhibitory activity. Conclusions: Our results suggest that BrDs warrant further investigation as natural immunomodulatory agents for control of inflammatory skin diseases.
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  <item rdf:about="https://ir.lib.ncu.edu.tw/handle/987654321/50860">
    <title>Toona sinensis (leaf extracts) inhibit vascular endothelial growth factor (VEGF)-induced angiogenesis in vascular endothelial cells</title>
    <link>https://ir.lib.ncu.edu.tw/handle/987654321/50860</link>
    <description>title: Toona sinensis (leaf extracts) inhibit vascular endothelial growth factor (VEGF)-induced angiogenesis in vascular endothelial cells abstract: Aim of the study: Toona sinensis is well known as a traditional Chinese medicine; also, it has been shown to exhibit anticancer and anti-inflammatory effects. This study was aimed at evaluating the anti-angiogenesis effect of the aqueous extracts of Toona sinensis (TS extracts) or gallic acid, a major component of IS extracts, against both VEGF-induced EA.hy 926 and human umbilical vein endothelial cells (HUVECs). Materials and methods: Anti-proliferative activity of IS extracts or gallic acid, was determined against EA.hy 926 and HUVECs by trypan blue exclusion method. Invasion, tube formation and chick chorioallantoic membrane assay were carried out to determine the in vitro and in vivo anti-angiogenic effects. Results: Non-cytotoxic concentration of IS extracts (50-100 mu g/mL) and gallic acid (5 mu g/mL) inhibited the proliferation of VEGF-stimulated EA.hy 926 and HUVECs. Inhibitory effects of IS extracts and gallic acid on angiogenesis were assessed by VEGF-induced migration/invasion and capillary-like tube formation by EA.hy 926 and HUVECs. Additionally, gelatin zymography assays showed that IS extracts and gallic acid suppressed the activity of metalloproteinase (MMP)-9 and MMP-2 activated by VEGF. In vivo, TS extracts and gallic acid strongly suppressed neovessel formation in the chorioallantoic membrane of chick embryos. Flow cytometry analyses and Western blot demonstrated that treatment with IS extracts and gallic acid induced Go/G, arrest in VEGF-stimulated EA.hy 926 cells via a reduction in the amounts of cyclin D1, cyclin E, CDK4, hyperphosphorylated retinoblastoma protein (pRb). VEGFR-2, and eNOS. Conclusions: These results support an anti-angiogenic activity of Toona sinensis that may contribute critically to its cancer and inflammation chemopreventive potentials. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
&lt;br&gt;</description>
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  <item rdf:about="https://ir.lib.ncu.edu.tw/handle/987654321/50857">
    <title>The management of incidental adnexal masses during cesarean section</title>
    <link>https://ir.lib.ncu.edu.tw/handle/987654321/50857</link>
    <description>title: The management of incidental adnexal masses during cesarean section</description>
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