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MMP-1 基因启动子区多态性对垂体腺瘤发生及侵袭性的影响。

The effect of polymorphisms in the promoter region of the MMP-1 gene on the occurrence and invasiveness of hypophyseal adenoma.

机构信息

Department of Neurosurgery, Tayfur Ata Sökmen Medical Faculty, Mustafa Kemal University, Hatay 31700, Turkey.

出版信息

Acta Neurochir (Wien). 2010 Sep;152(9):1611-7; discussion 1617. doi: 10.1007/s00701-010-0671-0. Epub 2010 May 4.

Abstract

BACKGROUND

The matrix metalloproteinase-1 enzyme (MMP-1, also called collagenase 1) plays a key role in turnover of collagen fibers in the intercellular matrix. Insertion of a guanine residue was found within the promoter region of the MMP-1 gene. We found that MMP-1 levels increased approximately twofold over normal when this insertion was present, enabling MMP-1 to facilitate tumor invasion and metastasis. MMP-1 is also believed to play a role in tumor development. The aim of our study is to investigate the effect of polymorphisms in the promoter region of the MMP-1 gene on the development of benign and invasive hypophyseal adenomas.

PATIENTS AND METHODS

Thirty patients with hypophyseal adenomas diagnosed by radiological examination underwent surgical removal, and the diagnosis was confirmed using immunohistochemical staining of the pathology specimens. We found that ten of these patients had invasive adenomas confirmed by radiological examination and immunohistochemical staining. DNA isolation was performed on all specimens, and 5-cc venous blood samples were obtained from all patients as well as 30 volunteers using the Qiagen QIAquick kit. Promoter regions of MMP-1 genes from the DNA samples were amplified using polymerase chain reaction (PCR) and primers designed for the site-directed mutation method. Following PCR, a guanine residue within the promoter region of the MMP-1 gene was identified using the restriction fragment length polymorphism method and the ALU I restriction enzyme. Three genotypes were detected in a genotyping assay: 2G/2G, 1G/2G, and 1G/1G.

RESULTS

Of the surgically treated patients, 36.6% had the 2G/2G genotype, 46.6% had the 1G/2G genotype, and 16.6% had the 1G/1G genotype. The 2G allele frequency was found to be 83.4%. In 90% of cases of invasive adenoma, a homozygous 2G/2G genotype was detected.

DISCUSSION

The risk for development of hypophyseal adenoma may be greater in patients with the 2G allele. In cases of existing hypophyseal adenoma, those with the homozygous 2G allele tend to be invasive.

摘要

背景

基质金属蛋白酶-1 酶(MMP-1,也称为胶原酶 1)在细胞外基质中胶原纤维的更新中起着关键作用。在 MMP-1 基因的启动子区域发现了一个鸟嘌呤残基的插入。我们发现,当存在这种插入时,MMP-1 的水平比正常情况下增加了约两倍,从而使 MMP-1 能够促进肿瘤的侵袭和转移。MMP-1 也被认为在肿瘤的发展中起作用。我们的研究目的是研究 MMP-1 基因启动子区域的多态性对良性和侵袭性垂体腺瘤发展的影响。

患者和方法

30 例经影像学检查诊断为垂体腺瘤的患者接受了手术切除,病理标本的免疫组织化学染色证实了这一诊断。我们发现,其中 10 例患者的影像学检查和免疫组织化学染色证实为侵袭性腺瘤。对所有标本进行 DNA 分离,并使用 Qiagen QIAquick 试剂盒从所有患者和 30 名志愿者中抽取 5 cc 静脉血样。使用聚合酶链反应 (PCR) 和针对定点突变方法设计的引物扩增 MMP-1 基因的启动子区域。PCR 后,使用限制性片段长度多态性方法和 ALU I 限制性内切酶鉴定 MMP-1 基因启动子区域内的鸟嘌呤残基。在基因分型试验中检测到三种基因型:2G/2G、1G/2G 和 1G/1G。

结果

手术治疗的患者中,2G/2G 基因型占 36.6%,1G/2G 基因型占 46.6%,1G/1G 基因型占 16.6%。2G 等位基因的频率为 83.4%。在 90%的侵袭性腺瘤病例中,检测到纯合 2G/2G 基因型。

讨论

携带 2G 等位基因的患者发生垂体腺瘤的风险可能更大。在存在垂体腺瘤的情况下,携带纯合 2G 等位基因的患者往往具有侵袭性。

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