Westerveld B D, Pals G, Defize J, Pronk J C, Frants R R, Ooms E C, Kreuning J, Eriksson A W, Meuwissen S G
Clin Genet. 1986 Sep;30(3):202-12. doi: 10.1111/j.1399-0004.1986.tb00596.x.
Electrophoretic pepsinogen A patterns were determined in gastric fundic mucosa biopsies from 601 patients with various gastric disorders and 25 healthy volunteers. Pepsinogen A patterns with an intense fraction 5 appeared to be associated with gastric cancer and premalignant changes of the stomach (p less than 10(-9)). In 60 individuals pepsinogen A patterns were determined in normal mucosa from different parts of the stomach. No differences were found between these patterns. In 29 out of 59 gastric cancer patients pepsinogen A could be demonstrated in the macroscopically malignant tissue. In two cases a different pattern compared with uninvolved fundic mucosa was observed. During a follow up study, major changes in the pepsinogen A pattern were observed in 7 out of 56 patients. In 8.6% of the examined patients urinary pepsinogen A patterns differed considerably as compared with the pattern observed in the gastric fundus. The results suggest that the highly significant association between intense Pg5 (the product of the D gene) and gastric cancer or its precursors may be caused by genetic as well as non-genetic factors.
对601例患有各种胃部疾病的患者以及25名健康志愿者的胃底黏膜活检组织进行了胃蛋白酶原A的电泳图谱测定。胃蛋白酶原A图谱中第5条带明显增强似乎与胃癌及胃的癌前病变有关(p<10⁻⁹)。对60名个体胃不同部位的正常黏膜进行了胃蛋白酶原A图谱测定,这些图谱之间未发现差异。59例胃癌患者中有29例在肉眼可见的恶性组织中检测到胃蛋白酶原A。有2例观察到与未受累胃底黏膜不同的图谱。在一项随访研究中,56例患者中有7例胃蛋白酶原A图谱出现了主要变化。在8.6%的受检患者中,尿胃蛋白酶原A图谱与胃底观察到的图谱相比有很大差异。结果表明,强烈的Pg5(D基因产物)与胃癌或其癌前病变之间的高度显著关联可能是由遗传因素和非遗传因素共同导致的。