首页> 外文期刊>The Journal of dermatology >Anaphylaxis caused by ingesting jellyfish in a subject with fermented soybean allergy: Possibility of epicutaneous sensitization to poly-gamma-glutamic acid by jellyfish stings
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Anaphylaxis caused by ingesting jellyfish in a subject with fermented soybean allergy: Possibility of epicutaneous sensitization to poly-gamma-glutamic acid by jellyfish stings

机译:在患有大豆过敏症的受试者中摄入水母引起的过敏反应:水母st伤皮肤对聚γ-谷氨酸致敏的可能性

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Background: Ameloblastoma is a frequent odontogenic neoplasm characterized by local invasiveness and high risk of recurrence. Reversion-inducing cysteine-rich protein with Kazal motifs (RECK) is a tumor suppressor that inhibits metastasis and angiogenesis. The aim of this study was to investigate effects of RECK overexpression on invasive potential in ameloblastoma cells. Methods: Lentiviral vectors containing human RECK gene were created and subsequently stably transfected into immortalized ameloblastoma cell line hTERT+-AM. Functional characteristics of hTERT+-AM cells with stable RECK overexpression included proliferation, migration, invasion, and regulation of matrix metalloproteinases (MMP)-2, MMP-9 measured by zymography or commercially available assays. Results: The stable and higher expression of RECK mRNA and protein (P 0.01) was detected in RECK-transfected hTERT+-AM cells. RECK overexpression caused a decrease in migration and invasion (P 0.01) for hTERT+-AM cells and a decrease in activity of MMP-2, MMP-9 (P 0.01). Proliferation was not affected by RECK overexpression (P 0.05). Conclusions: Overexpression of RECK gene significantly inhibited cell invasive ability of hTERT+-AM cells, suggesting RECK may be a new target for ameloblastoma treatment.
机译:背景:成釉细胞瘤是一种常见的牙源性肿瘤,其特征在于局部浸润性和高复发风险。具有Kazal基序(RECK)的诱导还原的富含半胱氨酸的蛋白是抑制转移和血管生成的肿瘤抑制因子。本研究的目的是研究RECK过表达对成釉细胞瘤细胞侵袭潜能的影响。方法:创建含有人RECK基因的慢病毒载体,然后将其稳定转染到永生化成釉细胞瘤细胞系hTERT + -AM中。具有稳定RECK过表达的hTERT + -AM细胞的功能特征包括通过酶谱法或市售测定法测量的基质金属蛋白酶(MMP)-2,MMP-9的增殖,迁移,侵袭和调节。结果:在RECK转染的hTERT + -AM细胞中,RECK mRNA和蛋白表达稳定,高表达(P <0.01)。 RECK的过表达导致hTERT + -AM细胞迁移和侵袭的减少(P <0.01)和MMP-2,MMP-9的活性的减少(P <0.01)。增殖不受RECK过表达的影响(P> 0.05)。结论:RECK基因的过表达显着抑制hTERT + -AM细胞的侵袭能力,提示RECK可能成为成釉细胞瘤治疗的新靶点。

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