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沙利度胺对人红系细胞γ珠蛋白基因表达的作用及相关机制研究 被引量:1
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作者 方栋 赖永榕 +3 位作者 刘容容 盘玲媛 杨阳 江雷 《广西医科大学学报》 CAS 2019年第5期734-738,共5页
目的:研究沙利度胺对人红系细胞γ珠蛋白基因表达的作用及相关调控机制。方法:采用一步液体培养法培养人红系细胞,以不同浓度沙利度胺(50 μmol/L、100 μmol/L、200 μmol/L、300 μmol/L)、100 μmol/L羟基脲(阳性对照)分别作用于人... 目的:研究沙利度胺对人红系细胞γ珠蛋白基因表达的作用及相关调控机制。方法:采用一步液体培养法培养人红系细胞,以不同浓度沙利度胺(50 μmol/L、100 μmol/L、200 μmol/L、300 μmol/L)、100 μmol/L羟基脲(阳性对照)分别作用于人红系细胞24 h、48 h、72 h、96 h,并设无任何干预的人红系细胞为空白对照组。采用实时荧光定量PCR(qPCR)法检测γ珠蛋白基因及转录因子BCL11A、KLF1、KLF2、GATA1基因的表达水平,Western blotting法检测γ珠蛋白的表达量。结果:作用于人红系细胞72 h后,100 μmol/L、200 μmol/L、300 μmol/L沙利度胺组γ珠蛋白基因相对表达量高于空白对照组,200 μmol/L、300 μmol/L沙利度胺组及阳性对照组γ珠蛋白表达量明显高于空白对照组(均 P <0.05);与空白对照组比较,200 μmol/L沙利度胺组BCL11A、KLF1基因表达明显下降,阳性对照组BCL11A基因表达下降,KLF2基因表达升高( P <0.05)。结论:沙利度胺能诱导体外人红系细胞γ珠蛋白基因表达,增加γ珠蛋白的生成,BCL11A、KLF1的下调可能是沙利度胺诱导γ珠蛋白基因表达的作用机制之一。 展开更多
关键词 沙利度胺 人红系细胞 γ珠蛋白基因 羟基脲
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Use of agents stimulating erythropoiesis in digestive diseases 被引量:2
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作者 Rosario Moreno López Beatriz Sicilia Aladrén Fernando Gomollón García 《World Journal of Gastroenterology》 SCIE CAS CSCD 2009年第37期4675-4685,共11页
Anemia is the most common complication of inflammatory bowel disease (IBD). Control and inadequate treatment leads to a worse quality of life and increased morbidity and hospitalization. Blood loss, and to a lesser ex... Anemia is the most common complication of inflammatory bowel disease (IBD). Control and inadequate treatment leads to a worse quality of life and increased morbidity and hospitalization. Blood loss, and to a lesser extent, malabsorption of iron are the main causes of iron def iciency in IBD. There is also a variable component of anemia related to chronic inflammation. The anemia of chronic renal failure has been treated for many years with recombinant human erythropoietin (rHuEPO), which significantly improves quality of life and survival. Subsequently, rHuEPO has been used progressively in other conditions that occur with anemia of chronic processes such as cancer, rheumatoid arthritis or IBD, and anemia associated with the treatment of hepatitis C virus. Erythropoietic agents complete the range of available therapeutic options for treatment of anemia associated with IBD, which begins by treating the basis of the inflammatory disease, along with intravenous iron therapy as f irst choice. In cases of resistance to treatment with iron, combined therapy with erythropoietic agents aims to achieve near-normal levels of hemoglobin/hematocrit (11-12 g/dL). New formulations of intravenous iron (iron carboxymaltose) and the new generation of erythropoietic agents (darbepoetin and continuous erythropoietin receptor activator) will allow better dosing with the same eff icacy and safety. 展开更多
关键词 Erythropoiesis-stimulating agents Recom-binant human erythropoietin DARBEPOETIN Continuous erythropoietin receptor activator Inflammatory bowel disease ANEMIA
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