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首页> 外文期刊>Journal of receptor and signal transduction research >Methylation-mediated gene silencing of suppressor of cytokine signaling-1 (SOCS-1) gene in esophageal squamous cell carcinoma patients of Kashmir valley
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Methylation-mediated gene silencing of suppressor of cytokine signaling-1 (SOCS-1) gene in esophageal squamous cell carcinoma patients of Kashmir valley

机译:克什米尔河谷食管鳞状细胞癌患者细胞因子信号传导抑制因子-1(SOCS-1)基因甲基化介导的基因沉默

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Context: Esophageal squamous cell carcinoma (ESCC) is a leading cause of cancer-related deaths in Jammu and Kashmir. The negative regulation of tumor suppressor gene leading to change in signaling pathway is one of the major mechanisms responsible for tumorigenic transformation. Objective: In the present study, the role of silencing of suppressor of cytokine signaling-1 (SOCS-1) gene, a negative regulator of JAK/STAT pathway, was analyzed in ESCC. Methods: The expression pattern of SOCS-1 gene was analyzed in esophageal tumor biopsies although normal adjacent tissues that served as controls. Reverse transcriptase polymerase chain reaction (RT-PCR), immunohistochemistry, methylation-specific PCR (MSP), and human papillomavirus (HPV) detection were performed to assess the expression pattern and promoter methylation of SOCS-1 gene including HPV status in a total of 75 surgically resected tissue specimens. Results: Compared with the level of SOCS-1 expression in normal tissues, 53% (40/75) of the tumor tissues expressed either undetectable or reduced SOCS-1 expression (>50% loss of expression), which was significantly associated with advanced clinical stage or severe histopathological grade of the disease (P<0.01). Aberrant promoter methylation of the SOCS-1 gene was found in 45% (34/75) of the esophageal tumor tissues, which was also found to be significantly associated with advanced stage of esophageal carcinoma (P<0.01). The prevalence of HPV infection was found in 19% of tumor cases, whereas no HPV could be detected in any of the normal adjacent tissues. Conclusion: Transcriptional inactivation of SOCS-1 gene, primarily due to its promoter hypermethylation although HPV infection, may play an important role in esophageal carcinogenesis in Kashmir.
机译:背景:食管鳞状细胞癌(ESCC)是查mu和克什米尔癌症相关死亡的主要原因。导致信号通路改变的抑癌基因的负调控是导致致瘤转化的主要机制之一。目的:本研究在ESCC中分析了JAK / STAT途径的负调控因子细胞因子信号传导抑制因子-1(SOCS-1)基因的沉默作用。方法:以正常邻近组织为对照,分析食管肿瘤活检组织中SOCS-1基因的表达模式。进行逆转录酶聚合酶链反应(RT-PCR),免疫组化,甲基化特异性PCR(MSP)和人乳头瘤病毒(HPV)检测,以评估SOCS-1基因的表达模式和启动子甲基化,包括HPV总数。 75个手术切除的组织标本。结果:与正常组织中SOCS-1表达水平相比,有53%(40/75)的肿瘤组织表达未检测到或降低了SOCS-1表达(> 50%表达损失),这与晚期该疾病的临床分期或严重的组织病理学分级(P <0.01)。在食管肿瘤组织中有45%(34/75)发现SOCS-1基因的异常启动子甲基化,也与食管癌的晚期显着相关(P <0.01)。在19%的肿瘤病例中发现了HPV感染的流行,而在任何正常的相邻组织中均未检测到HPV。结论:SOCS-1基因的转录失活主要是由于其启动子甲基化,尽管HPV感染,但在克什米尔食管癌变中可能起重要作用。

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