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40岁以下胃癌患者的p53基因:突变率较低,但与贲门部位有关。

The p53 gene in patients under the age of 40 with gastric cancer: mutation rates are low but are associated with a cardiac location.

作者信息

Rugge M, Shiao Y H, Busatto G, Cassaro M, Strobbe C, Russo V M, Leo G, Parenti A R, Scapinello A, Arslan P, Egarter-Vigl E

机构信息

Department of Oncology and Surgical Sciences, University of Padova, ULSS15-Regione Veneto, Italy.

出版信息

Mol Pathol. 2000 Aug;53(4):207-10. doi: 10.1136/mp.53.4.207.

Abstract

BACKGROUND

Determining both the frequency and the spectrum of p53 gene mutation in young patients with gastric cancer might provide clues to the host related genetic mechanism(s) in gastric carcinogenesis.

PATIENTS AND METHODS

p53 mutations were assessed (by means of polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP), followed by DNA sequencing) in a cohort of 105 consecutive Italian patients in whom gastric cancer was ascertained before the age of 41.

RESULTS

A low prevalence of p53 mutations (eight of 105) was observed, with no significant difference between intestinal (three of 31; 10%) and diffuse (five of 74; 7%) phenotypes. A significantly higher prevalence of p53 mutations was associated with the cardiac location (odds ratio, 7.09; confidence interval, 1.56 to 32.11). In all but one case, p53 mutations were associated with a stage higher than I. All eight mutations were located at CpG sites, where G : C to A : T transitions have been associated with frequent methylation at the C5 position of cytosine.

CONCLUSIONS

These findings show that, unlike what has been consistently demonstrated in the general population, p53 mutations are uncommon in gastric cancer occurring in young patients, and in such patients, p53 alterations are significantly associated with the cardiac location.

摘要

背景

确定年轻胃癌患者中p53基因突变的频率和谱型可能为胃癌发生过程中宿主相关的遗传机制提供线索。

患者与方法

对105例连续的意大利患者(确诊为胃癌时年龄在41岁之前)进行p53基因突变评估(采用聚合酶链反应-单链构象多态性分析(PCR-SSCP),随后进行DNA测序)。

结果

观察到p53基因突变的发生率较低(105例中有8例),肠型(31例中有3例;10%)和弥漫型(74例中有5例;7%)表型之间无显著差异。p53基因突变的发生率在贲门部显著更高(优势比,7.09;可信区间,1.56至32.11)。除1例之外,所有p53基因突变均与高于I期相关。所有8个突变均位于CpG位点,在该位点G:C到A:T的转换与胞嘧啶C5位置的频繁甲基化有关。

结论

这些发现表明,与在普通人群中一直观察到的情况不同,p53基因突变在年轻患者发生的胃癌中并不常见,并且在这类患者中,p53改变与贲门部位置显著相关。

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