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幽门螺杆菌阳性和阴性胃炎中突变型p53表达及凋亡活性与肠化生存在的相关性

Mutant p53 expression and apoptotic activity of Helicobacter pylori positive and negative gastritis in correlation with the presence of intestinal metaplasia.

作者信息

Unger Zsuzsa, Molnár Béla, Prónai László, Szaleczky Erika, Zágoni Tamás, Tulassay Zsolt

机构信息

Semmelweis University, Faculty of Medicine, 2nd Department of Internal Medicine, 1088 Budapest, Szentkirályi út 46, Hungary.

出版信息

Eur J Gastroenterol Hepatol. 2003 Apr;15(4):389-93. doi: 10.1097/00042737-200304000-00009.

Abstract

BACKGROUND

Mutation of the p53 gene is detectable in most cases of gastric cancer, as it is the most common genetic alteration in human malignancies. It is also well documented that Helicobacter pylori infection plays an important role in gastric carcinogenesis. There is still no clarification, however, concerning how genetic instability influences the homeostasis of gastric epithelium. We have studied the effect of H. pylori infection on apoptosis of the antral epithelium in the presence/absence of intestinal metaplasia and the expression of the p53 oncoprotein. The relationship between these two processes is analysed.

METHODS

Antral biopsies were taken from 36 patients who underwent routine upper endoscopy (17 men, 19 women, mean age 61.0 years). The biopsies were fixed in formalin and embedded in paraffin. Patients were classified into two histological groups: (1) as chronic gastritis without intestinal metaplasia (n = 19), and (2) chronic gastritis with intestinal metaplasia (n = 17). An immunohistochemical method was used to detect the expression of p53 oncoprotein, and the terminal transferase mediated dUTP nick end-labelling (TUNEL) method was used to detect apoptotic cells.

RESULTS

In the absence of intestinal metaplasia, both the apoptotic index (0.0272 +/- 0.011 vs 0.0128 +/- 0.006) and expresssion of p53 (35.55 +/- 31.16 vs 18.33 +/- 19.65) were significantly higher in H. pylori positive cases compared to H. pylori negative cases. In the presence of intestinal metaplasia, p53 expression was further increased (P < 0.05), but apoptosis was similar to that observed in H. pylori negative gastritis without intestinal metaplasia. In the presence of intestinal metaplasia, H. pylori infection did not influence apoptosis (0.013 +/- 0.004 vs 0.011 +/- 0.004), or p53 ratio (70.16 +/- 22.54 vs 68.50 +/- 28.96). In the sequence of gastritis-intestinal metaplasia the two indices show a close negative correlation (P < 0.05).

CONCLUSION

In the absence of intestinal metaplasia H. pylori infection increases both apoptotic activity and expression of p53 oncoprotein in the gastric mucosa. The lack of increased apoptosis with a higher p53 expression in the presence of intestinal metaplasia suggests an increased genetic instability and also may suggest that mutation of the p53 gene is an early step in the multistep process of gastric carcinogenesis.

摘要

背景

在大多数胃癌病例中可检测到p53基因的突变,因为它是人类恶性肿瘤中最常见的基因改变。幽门螺杆菌感染在胃癌发生过程中起重要作用也有充分的文献记载。然而,关于基因不稳定性如何影响胃上皮细胞的稳态仍未阐明。我们研究了幽门螺杆菌感染在存在/不存在肠化生的情况下对胃窦上皮细胞凋亡及p53癌蛋白表达的影响。分析了这两个过程之间的关系。

方法

对36例行常规上消化道内镜检查的患者(17例男性,19例女性,平均年龄61.0岁)取胃窦活检组织。活检组织用福尔马林固定并石蜡包埋。患者分为两个组织学组:(1)无肠化生的慢性胃炎(n = 19),(2)有肠化生的慢性胃炎(n = 17)。采用免疫组化方法检测p53癌蛋白的表达,采用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记法(TUNEL法)检测凋亡细胞。

结果

在无肠化生的情况下,幽门螺杆菌阳性病例的凋亡指数(0.0272±0.011对0.0128±0.006)和p53表达(35.55±31.16对18.33±19.65)均显著高于幽门螺杆菌阴性病例。在有肠化生的情况下,p53表达进一步增加(P < 0.05),但凋亡情况与无肠化生的幽门螺杆菌阴性胃炎相似。在有肠化生的情况下,幽门螺杆菌感染不影响凋亡(0.013±0.004对0.011±0.004)或p53比率(70.16±22.54对68.50±28.96)。在胃炎-肠化生的过程中,这两个指标呈密切负相关(P < 0.05)。

结论

在无肠化生的情况下,幽门螺杆菌感染增加胃黏膜的凋亡活性和p53癌蛋白的表达。在有肠化生的情况下,凋亡未增加而p53表达升高提示基因不稳定性增加,也可能提示p53基因的突变是胃癌发生多步骤过程中的早期步骤。

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