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纤溶酶原激活物抑制剂-1多态性与口腔癌风险增加相关。

Plasminogen activator inhibitor-1 polymorphism is associated with increased risk for oral cancer.

作者信息

Vairaktaris E, Yapijakis C, Serefoglou Z, Vylliotis A, Ries J, Nkenke E, Wiltfang J, Derka S, Vassiliou S, Springer I, Kessler P, Neukam F W

机构信息

Department of Maxillofacial Surgery, University of Athens Medical School, Vas. Sofias 93 and Dim. Soutsou 1, Athens 11521, Greece.

出版信息

Oral Oncol. 2006 Oct;42(9):888-92. doi: 10.1016/j.oraloncology.2005.12.005. Epub 2006 May 26.

Abstract

In light of the recently observed contribution of thrombosis-related factors to carcinogenesis, we investigated the possible association of plasminogen activator inhibitor-1 (PAI-1) with increased risk for oral cancer. In DNA samples of 104 patients with oral squamous cell carcinoma and 106 healthy controls of comparable ethnicity, age and sex, we studied the 4G/5G polymorphism in the PAI-1 gene, which affects its expression. The mutant 4G allele and carrier frequencies were significantly increased in patients compared to controls (65.9% versus 49.5%; 88.5% versus 69.8% respectively, P<0.01). That increase was even higher in patients with a positive family history for thrombophilia or without one for cancer (P<0.001). Interestingly, significant difference from controls was observed only in patients with cancer stages I and II. These findings suggest that the 4G allele, by resulting in higher PAI-1 expression, is a major contributing factor in early stages of oral oncogenesis. Possibly, increased PAI-1 promotes initial development of oral cancer through regulation of cell detachment and delays further tumor progression by inhibiting vascularization.

摘要

鉴于最近观察到血栓形成相关因素对致癌作用的影响,我们研究了纤溶酶原激活物抑制剂-1(PAI-1)与口腔癌风险增加之间的可能关联。在104例口腔鳞状细胞癌患者和106例种族、年龄和性别匹配的健康对照者的DNA样本中,我们研究了影响PAI-1基因表达的4G/5G多态性。与对照组相比,患者中突变型4G等位基因和携带者频率显著增加(分别为65.9%对49.5%;88.5%对69.8%,P<0.01)。在有血栓形成倾向阳性家族史或无癌症家族史的患者中,这种增加甚至更高(P<0.001)。有趣的是,仅在I期和II期癌症患者中观察到与对照组的显著差异。这些发现表明,4G等位基因通过导致更高的PAI-1表达,是口腔肿瘤发生早期的一个主要促成因素。可能,PAI-1增加通过调节细胞脱离促进口腔癌的初始发展,并通过抑制血管生成延迟肿瘤的进一步进展。

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