血管瘤组织总ERK1/2及磷酸化ERK1/2的免疫印迹检测  被引量:2

Immunoblotting Detection of Total ERK1/2 and Phospho-ERK1/2 in Hemangioma

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作  者:冯进云[1] 陈小文[2] 李萍[1] 彭振辉[3] 

机构地区:[1]深圳市儿童医院皮肤科,广东深圳518026 [2]深圳市儿童医院儿研所,广东深圳5180263 [3]西安交通大学第二医院皮肤科,陕西西安710004

出  处:《中国皮肤性病学杂志》2013年第2期115-117,共3页The Chinese Journal of Dermatovenereology

基  金:深圳市科技计划项目(201003140)

摘  要:目的检测细胞外信号调节激酶1/2(总ERK1/2)及磷酸化ERK1/2(p-ERK1/2)在血管瘤组织中的表达并探讨其意义。方法应用免疫印迹法检测10例增生期血管瘤组织和8例退化期血管瘤组织总ERK1/2及p-ERK1/2的蛋白表达。结果增生期血管瘤组织总ERK1/2的蛋白表达(0.87±0.14)与退化期血管瘤组织总ERK1/2的蛋白表达(0.79±0.05)差异无统计学意义(P>0.05);增生期血管瘤组织p-ERK1/2的蛋白表达(0.44±0.04)明显高于与退化期血管瘤组织p-ERK1/2的蛋白表达(0.23±0.08),差异有统计学意义(P<0.01)。结论血管瘤增生与ERK活性增高及ERK通路激活有关。Objective To investigate protein expression of total extraeellular sigual-regulated kinasel/2 ( total ERK1/ 2) and phospho-extraeellular signal-regalated kinasel/2 (p-ERK1/2) in hemangiomas, and to explore their role in the development of hemangiomas. Methods Total ERK1/2 and p-ERK1/2 protein levels in 10 pro- liferating phase hemangiomas and in 8 involuting phase hemangiomas were assessed by Immunoblotting. Re- suits There was no significant difference between total ERK1/2 protein levels(0.87±0.14)in proliferating hemangioma and those(0.79 ± 0.05 ) in involuting hemangioma ( P 〉 0.05 ). The p-ERK1/2 protein levels ( 0.44 ± 0.04 ) in proliferating hemangioma were significantly higher than those ( 0.23 ± 0.08 ) in involuting hemangioma (P 〈 0.01 ). Conclusion The aetivation of ERK1/2 and ERK signalling pathway may be re- lated with hemangiomatous proliferation.

关 键 词:血管瘤 细胞外信号调节激酶 磷酸化细胞外信号调节激酶 免疫印迹 

分 类 号:R739.5[医药卫生—肿瘤]

 

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