卵巢巧克力囊肿介入治疗前后血清IL-6、JunB、beta-1、4-GalT-Ⅰ的表达差异

来源 :中国超声医学杂志 | 被引量 : 0次 | 上传用户:wuheman
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
目的超声引导下95%医用酒精硬化治疗卵巢巧克力囊肿(巧囊)前后血清IL-6、JunB、beta-1、4-GalT-Ⅰ的表达差异。方法选取超声引导下酒精硬化治疗的9例巧囊患者,术前、后3个月肘静脉采血标本,采用NimbleGen全基因组表达谱芯片法检测,筛选出治疗前、后差异表达的显著因子,并分析有显著表达差异因子的功能及通路与巧囊介入治疗的相关性。结果在NimbleGen全基因组表达谱芯片检测中筛选出IL-6、JunB及beta-1、4-GalT-Ⅰ;酒精硬化治疗巧囊术可使这3条因子表达下调,它们参与的免疫调节、血管形成、细胞粘连等功能与巧囊的发病机制具有相关性,并通过7条信号通路发挥作用。结论巧囊患者血清IL-6、JunB及beta-1,4-GalT-Ⅰ在酒精硬化治疗后呈下调表达,具有从分子水平评价介入治疗疗效的价值。 Objective To investigate the difference of serum IL-6, JunB, beta-1, 4-GalT-Ⅰ levels before and after treatment with 95% alcoholic sclerosis on ovarian chocolate cysts. Methods 9 cases of clever cystic patients undergoing ultrasound guided alcohol sclerotherapy were selected. Blood samples were collected from the elbow venous before and 3 months after operation. NimbleGen whole genome cDNA microarray was used to screen the significant differentially expressed genes Analysis of significant differences in the expression of the function of factors and pathways involved with the intervention of clever capsule. RESULTS: IL-6, JunB and beta-1,4-GalT-I were screened by NimbleGen genome-wide expression microarray. Alcohol sclerotherapy and cystic surgery could down-regulate the expression of these three factors and participate in the immunomodulation and vascular Formation, cell adhesion and other functions with the pathogenesis of Qiao capsule has relevance, and through the seven signaling pathway play a role. Conclusion The serum levels of IL-6, JunB and beta-1,4-GalT-I in patients with Qiao capsule are down-regulated after alcoholic sclerosis treatment, which has the value of evaluating the efficacy of interventional therapy at the molecular level.
其他文献
目的:构建带myc标签的Six1基因的真核表达载体,获得myc-Six1融合蛋白,并对其生物学功能进行初步检测。方法:以本实验室保存的乳腺文库为模板,采用PCR技术扩增Six1编码序列,将其插入
目的:构建带myc标签的人激活转录因子5(ATF5)的真核表达载体,获得myc-ATF5融合蛋白,并对其生物学功能进行初步检测。方法:以本实验室保存的带有XL5标签的ATF5质粒为模板,采用PCR技术
目的:克隆、表达人vasorin(VASN)蛋白。方法:利用PCR方法从HepG2细胞的cDNA中扩增获得目的基因,并插入带有6×His标签的原核高效可溶性表达载体pET28a中,构建重组表达质粒pET28a-VA
目的:在大肠杆菌中可溶性表达艰难梭菌毒素B羧基端(TcdB-c),免疫产蛋鸡,获得针对TcdB-c的卵黄抗体(IgY)。方法:人工合成TcdB-c的基因,将其克隆至pET32b(+)载体中,转化大肠杆菌BL21(DE3),诱导