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首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >HMSH2 and HMSH6 gene expression profiles in colorectal adenocarcinoma in patients up to 50 years of age
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HMSH2 and HMSH6 gene expression profiles in colorectal adenocarcinoma in patients up to 50 years of age

机译:HMSH2和HMSH6基因在50岁以下大肠腺癌中的表达谱

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摘要

Lynch syndrome, previously called hereditary non-polyposis colorectal cancer (HNPCC), is a major mortality threat. It is an autosomal dominant disease which is caused by a germline mutation in the DNA mismatch repair (MMR), especially in patients aged up to 50 years. Such mutation more frequently occurs in the hMSH2 gene (38-40%) and less frequently in the hMSH6 gene (14-16%). These mutations, when associated with the patient's lifestyle, may reveal a considerable variability in the disease manifestations, such as the degrees of penetrance and clinical aggressiveness. The aim of this study is to analyze the expression of DNA MMR genes, and correlate this expression with the clinical and anatomopathological findings of the neoplasia in patients aged between 39 and 49 years. A total of 45 patients were included: (48.9%) males and (51.1%) females, and they all underwent resection of a colorectal adenocarcinoma. The tissue microarray technique was used to analyze the relative and absolute expression of hMSH2 and hMSH6. Amsterdam II criteria for the diagnosis of HNPCC were obtained from the data provided by medical records and interviews with patients. hMSH2 and hMSH6 was expressed in all patients, which correlated between each other (RHO = 0.669 and p < 0.001) but not to age. There is a positive correlation between the expressions of males (RHO = 0.673 and p = 0.001) and females (RHO = 0.006 and p < 0.001). It is possible to evaluate the expression of MMR genes in embedded anatomopathological samples. Gene expressions correlated between each other and to the sex of the patients, but no difference in relation to age. (C) 2016 Elsevier Masson SAS. All rights reserved.
机译:Lynch综合征,以前称为遗传性非息肉性结直肠癌(HNPCC),是主要的死亡威胁。它是一种常染色体显性遗传疾病,由DNA错配修复(MMR)中的种系突变引起,尤其是在50岁以下的患者中。此类突变在hMSH2基因中的发生频率较高(38-40%),在hMSH6基因中的发生频率较低(14-16%)。当与患者的生活方式相关时,这些突变可能揭示疾病表现的相当大的可变性,例如外显度和临床侵略性。这项研究的目的是分析DNA MMR基因的表达,并将其与39到49岁患者的肿瘤形成的临床和解剖病理学发现相关联。总共包括45名患者:(48.9%)男性和(51.1%)女性,他们都接受了结直肠腺癌的切除术。组织芯片技术用于分析hMSH2和hMSH6的相对和绝对表达。根据病历和患者访谈提供的数据,获得了阿姆斯特丹II型HNPCC诊断标准。 hMSH2和hMSH6在所有患者中均表达,彼此之间相关(RHO = 0.669,p <0.001),但与年龄无关。男性(RHO = 0.673和p = 0.001)和女性(RHO = 0.006和p <0.001)之间的表达呈正相关。有可能评估MMR基因在嵌入式解剖病理学样本中的表达。基因表达彼此之间以及患者性别之间相关,但在年龄方面无差异。 (C)2016 Elsevier Masson SAS。版权所有。

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