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PTEN基因改变对胆囊癌患者的影响。

Effects of PTEN gene alteration in patients with gallbladder cancer.

作者信息

Ali Asgar, Mishra Pramod Kumar, Sharma Sadhana, Arora Asit, Saluja Sundeep Singh

机构信息

Department of Biochemistry, All India Institute of Medical Sciences (AIIMS), Patna, India.

Department of Gastrointestinal Surgery, G.B. Pant Hospital, New Delhi, India.

出版信息

Cancer Genet. 2015 Dec;208(12):587-94. doi: 10.1016/j.cancergen.2015.09.007. Epub 2015 Sep 28.

DOI:10.1016/j.cancergen.2015.09.007
PMID:26586294
Abstract

Gallbladder cancer (GBC) is an aggressive malignancy usually diagnosed in an advanced stage. We investigated the effects of alterations of the phosphatase and tensin homologue (PTEN) gene on the occurrence and development of GBC, which has not been previously reported. A total 141 cases of GBC were analyzed for mutation, expression, and methylation across the nine exons of the PTEN gene. DNA sequencing methods were applied for mutation detection, whereas protein expression and methylation status were evaluated by immunohistochemical and methylation-specific PCR analysis, respectively. Novel PTEN mutations were observed in 6.3% of cases (9/141), and they included two silent mutations. In mutant cases, according to changes in codons, the respective amino acid sequences were also changed, which caused of proteins. A high percentage (72%) of loss of protein expression was observed more often in cases than in control samples. Interestingly, all nine cases with mutations showed loss of PTEN expression, whereas four of these nine cases showed positive promoter methylation. Hypermethylation was significantly more common in older patients than in younger ones (P<0.02). These findings suggest that PTEN mutations and inactivation may play an important role in the development and progression of gallbladder carcinoma.

摘要

胆囊癌(GBC)是一种侵袭性恶性肿瘤,通常在晚期被诊断出来。我们研究了磷酸酶和张力蛋白同源物(PTEN)基因改变对胆囊癌发生发展的影响,此前尚未有相关报道。对总共141例胆囊癌病例进行了PTEN基因九个外显子的突变、表达和甲基化分析。采用DNA测序方法检测突变,分别通过免疫组织化学和甲基化特异性PCR分析评估蛋白质表达和甲基化状态。在6.3%的病例(9/​​141)中观察到新的PTEN突变,其中包括两个沉默突变。在突变病例中,根据密码子的变化,相应的氨基酸序列也发生了变化,从而导致蛋白质的变化。与对照样本相比,在病例中更常观察到高比例(72%)的蛋白质表达缺失。有趣的是,所有九个突变病例均显示PTEN表达缺失,而这九个病例中有四个显示启动子甲基化阳性。老年患者的高甲基化明显比年轻患者更常见(P<0.02)。这些发现表明,PTEN突变和失活可能在胆囊癌的发生和发展中起重要作用。

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