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胃癌患者胃黏膜中胃蛋白酶原A3基因表达缺失。

Absence of pepsinogen A3 gene expression in the gastric mucosa of patients with gastric cancer.

作者信息

Kuipers E J, Peña A S, Crusius J B, Defize J, van der Stoop P, Meuwissen S G, Pals G

机构信息

Department of Gastroenterology, Vrije Universiteit, Amsterdam, The Netherlands.

出版信息

J Clin Pathol. 1995 Apr;48(4):376-9. doi: 10.1136/jcp.48.4.376.

DOI:10.1136/jcp.48.4.376
PMID:7615861
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC502560/
Abstract

AIMS

To investigate the expression of pepsinogen A3 (Pg3) encoding genes in the gastric mucosa of normal controls and subjects with atrophic gastritis and gastric cancer.

METHODS

One hundred and fifty nine patients underwent upper gastrointestinal endoscopy with sampling of gastric biopsy specimens and serum. Pg3 isoproteins were determined by electrophoresis in serum and gastric mucosal biopsy specimens. Pg3 encoding genes were assessed by PCR in DNA obtained from peripheral blood.

RESULTS

One hundred and one subjects (82 normal histology/chronic gastritis, 17 atrophic gastritis, two gastric cancer) showed a pepsinogen phenotype with presence of Pg3 and a corresponding pepsinogen genotype with presence of Pg3 encoding genes. Fifty eight subjects showed a phenotype lacking Pg3. In 39 of them (23 normal histology/chronic gastritis, 11 atrophic gastritis, five gastric cancer), a corresponding genotype without Pg3 encoding genes was found. However, in the remaining 19 subjects (4 normal histology/chronic gastritis, nine atrophic gastritis, six gastric cancer); Pg3 encoding genes were demonstrable in the absence of Pg3 production.

CONCLUSIONS

Unexpressed Pg3 encoding genes can be shown in many cases of atrophic gastritis and gastric cancer, but rarely in healthy controls and subjects with superficial gastritis. The correlation of atrophic gastritis and gastric cancer with a pepsinogen phenotype lacking Pg3 can be explained by loss of expression of Pg3 encoding genes throughout the complete gastric mucosa. The mechanism of such loss and the importance as a marker for premalignant degeneration have to be elucidated.

摘要

目的

研究胃蛋白酶原A3(Pg3)编码基因在正常对照者、萎缩性胃炎患者及胃癌患者胃黏膜中的表达情况。

方法

159例患者接受上消化道内镜检查,并采集胃活检标本和血清。通过血清及胃黏膜活检标本电泳测定Pg3同工酶。采用聚合酶链反应(PCR)在外周血DNA中评估Pg3编码基因。

结果

101例受试者(82例组织学正常/慢性胃炎、17例萎缩性胃炎、2例胃癌)表现出含有Pg3的胃蛋白酶原表型及相应的含有Pg3编码基因的胃蛋白酶原基因型。58例受试者表现出缺乏Pg3的表型。其中39例(23例组织学正常/慢性胃炎、11例萎缩性胃炎、5例胃癌)发现相应的缺乏Pg3编码基因的基因型。然而,在其余19例受试者(4例组织学正常/慢性胃炎、9例萎缩性胃炎、6例胃癌)中,虽无Pg3产生,但可检测到Pg3编码基因。

结论

在许多萎缩性胃炎和胃癌病例中可显示未表达的Pg3编码基因,但在健康对照者和浅表性胃炎患者中很少见。萎缩性胃炎和胃癌与缺乏Pg3的胃蛋白酶原表型之间的相关性可通过整个胃黏膜中Pg3编码基因表达缺失来解释。这种缺失的机制及其作为癌前退变标志物的重要性有待阐明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b0f/502560/68a430d9d729/jclinpath00229-0097-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b0f/502560/bff01e1e47c2/jclinpath00229-0096-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b0f/502560/68a430d9d729/jclinpath00229-0097-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b0f/502560/bff01e1e47c2/jclinpath00229-0096-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b0f/502560/68a430d9d729/jclinpath00229-0097-a.jpg

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本文引用的文献

1
Gastric chief cell-specific transcription of the pepsinogen A gene.
Eur J Biochem. 1993 May 1;213(3):1283-96. doi: 10.1111/j.1432-1033.1993.tb17880.x.
2
Gastric neoplasms and pepsinogen phenotypes.胃肿瘤与胃蛋白酶原表型
Br J Cancer. 1982 Aug;46(2):289-90. doi: 10.1038/bjc.1982.195.
3
Relationships among serum pepsinogen I, serum pepsinogen II, and gastric mucosal histology. A study in relatives of patients with pernicious anemia.血清胃蛋白酶原I、血清胃蛋白酶原II与胃黏膜组织学之间的关系。一项针对恶性贫血患者亲属的研究。
Gastroenterology. 1982 Jul;83(1 Pt 2):204-9.
4
The pepsinogens of human gastric mucosa.人类胃黏膜的胃蛋白酶原
Gut. 1973 Nov;14(11):850-5. doi: 10.1136/gut.14.11.850.
5
Urinary pepsinogen I: A multigene family?尿胃蛋白酶原I:一个多基因家族?
Prog Clin Biol Res. 1985;173:23-30.
6
Qualitative and quantitative determinations of pepsinogen I in gastric cancer and premalignant changes of the stomach.胃癌及胃黏膜癌前病变中胃蛋白酶原I的定性与定量测定
Prog Clin Biol Res. 1985;173:201-12.
7
Clinical significance of pepsinogen A isozymogens, serum pepsinogen A and C levels, and serum gastrin levels.胃蛋白酶原A同工酶、血清胃蛋白酶原A和C水平以及血清胃泌素水平的临床意义。
Cancer. 1987 Mar 1;59(5):952-8. doi: 10.1002/1097-0142(19870301)59:5<952::aid-cncr2820590517>3.0.co;2-g.
8
Heterochromatinization of human X-chromosomes: classification of replication profile.
Clin Genet. 1986 Aug;30(2):108-11. doi: 10.1111/j.1399-0004.1986.tb00577.x.
9
Discrepancies between gastric mucosal and urinary pepsinogen A patterns and in vitro synthesis and secretion of human pepsinogen.胃黏膜和尿液中胃蛋白酶原A模式与人胃蛋白酶原体外合成及分泌之间的差异。
Dig Dis Sci. 1988 Feb;33(2):135-43. doi: 10.1007/BF01535723.
10
Changes in rat and human pepsinogen phenotypes induced by N'-methyl-N'nitro-N-nitrosoguanidine.
Cancer. 1988 Nov 1;62(9):1958-61. doi: 10.1002/1097-0142(19881101)62:9<1958::aid-cncr2820620915>3.0.co;2-f.