首页> 外文期刊>Cellular oncology >Aberrant promoter methylation and loss of suppressor of cytokine signalling-1 gene expression in the development of uterine cervical carcinogenesis.
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Aberrant promoter methylation and loss of suppressor of cytokine signalling-1 gene expression in the development of uterine cervical carcinogenesis.

机译:子宫颈癌变发展中异常启动子甲基化和细胞因子信号1基因表达抑制子的丧失。

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摘要

Cervical cancer is a leading cause of cancer related deaths in women worldwide caused due to infection of high-risk human papillomaviruses. As JAK/STAT signalling pathway has been shown to play an important role during carcinogenesis, we studied the role of silencing of Suppressor of Cytokine Signalling-1 (SOCS-1) gene, a negative regulator of JAK/STAT pathway in cervical cancer.The expression pattern of SOCS-1 mRNA and protein was analyzed in different stages of cervical tumor biopsies while normal cervical tissues served as controls. RT-PCR, immunohistochemistry and methylation-specific PCR (MSP) were performed to assess the expression pattern and promoter methylation of SOCS-1 gene in a total of 120 fresh surgically resected cervical tissue specimens comprising precancer (n?=?12), cancer (n?=?78) and normal controls (n?=?30).Compared with expression of SOCS-1 in normal tissues, 64% of the tumor tissues expressed either undetectable or reduced expression. Aberrant promoter methylation of SOCS-1 was found in 61% of the cervical tumor tissues. SOCS-1 expression and methylation were significantly associated with severity of the disease (p?
机译:宫颈癌是全球女性因感染高危人乳头瘤病毒引起的癌症相关死亡的主要原因。由于已证明JAK / STAT信号通路在致癌过程中起着重要作用,因此我们研究了沉默细胞因子信号传导-1(SOCS-1)基因(宫颈癌JAK / STAT通路的负调控因子)的沉默的作用。以正常宫颈组织为对照,分析宫颈癌活检不同阶段SOCS-1 mRNA和蛋白的表达模式。进行了RT-PCR,免疫组化和甲基化特异性PCR(MSP),以评估总共120份包含癌前病变(n≥12),经手术切除的新鲜宫颈组织标本中SOCS-1基因的表达模式和启动子甲基化。 (n≥78)和正常对照(≥30)。与SOCS-1在正常组织中的表达相比,64%的肿瘤组织表达无法检测或表达降低。在61%的宫颈肿瘤组织中发现了SOCS-1的异常启动子甲基化。 SOCS-1的表达和甲基化与疾病的严重程度显着相关(p <0.01)。我们首次证明了由于高甲基化和与HPV感染的协同作用,SOCS-1基因的转录失活可能起重要作用。在宫颈癌中。

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