机构地区:[1]郑州大学第一附属医院肿瘤科,河南郑州450052 [2]郑州大学公共卫生学院营养与食品卫生学教研室,河南郑州450001
出 处:《中华肿瘤防治杂志》2013年第6期448-452,共5页Chinese Journal of Cancer Prevention and Treatment
摘 要:目的:研究胃癌组织中丝氨酸/苏氨酸激酶(AKT-2)和胃蛋白酶原C(PGC)的表达及其临床意义分析。方法:应用免疫组化SP检测75例胃癌组织、20例萎缩性胃炎组织和15例正常胃黏膜组织标本中AKT-2蛋白和PGC的表达,采用χ2检验分析临床病理因素与上述指标的相关性。结果:胃癌、萎缩性胃炎和胃正常黏膜组织中AKT-2阳性表达率分别为70.7%(53/75)、38.9%(7/20)和26.7%(4/15),在胃癌组织中的表达明显高于萎缩性胃炎组织和胃正常黏膜组织(P值分别为0.003和0.001),但后两者之间差异无统计学意义(P=0.875),且与胃癌的分化程度、浸润深度、淋巴结转移及临床分期有关,P值分别为0.019,0.017,0.027和0.030;胃癌、萎缩性胃炎和胃正常黏膜组织中PGC阳性表达率分别为9.3%(7/75)、65.0%(13/20)和100.0%(15/15),在胃癌组织中的表达明显高于萎缩性胃炎组织和胃正常黏膜组织(P值分别为0.000和0.000),后两者差异有统计学意义(P=0.033),且与胃癌的分化程度及临床分期有关,P值分别为0.037和0.044;胃癌组织中AKT-2与PGC的表达存在负相关性,r=-0.297,P=0.01。结论:胃癌组织中AKT-2的表达明显高于萎缩性胃炎组织和胃正常黏膜组织,而胃癌组织中PGC的表达明显低于萎缩性胃炎组织和胃正常黏膜组织。因此,AKT-2的过表达及PGC的低表达在胃癌早期诊断中发挥重要作用。OBJECTIVE:To study expression of Serine/Threonine Kinase (AKT-2) and Pepsinogen C(PGC) in gas- tric carcinoma,and analyze its clinical significance. METHODS: Immunohistochemistry was used to examine expression of AKT-2 and PGC in 75 gastric carcinoma,20 atrophic gastritis tissues and 15 para-earcinoma normal mucosa tissues. The correlation between AKT-2,PGC and the clinical pathologic factors was analyzed by chi-square test. RESULTS: The posi- tive rates of AKT-2 in gastric carcinoma, atrophic gastritis tissues and para-carcinoma normal mucosa tissues gradually de- clined,were 70.7%(53/75) to 38.9%(7/20) and 26.7%(4/15). The expression of AKT-2 in gastric carcinoma tissues was significantly higher than that in atrophic gastritis tissues(P=0. 003) and normal tissue (P=0. 001) ,but there was no significant different between the latter two groups (P= 0. 875). Expression of AKT-2 was significantly correlated with differentiation status (P = 0.019), infiltration depth (P = 0.017), lymph node metastasis (P = 0.027) and clinical stage of the cancer (P=0. 030). The positive rates of PGC in gastric carcinoma,atrophic gastritis tissues and para-carcinoma nor- mal mucosa tissues were 9.3~ (7/75) ,65.0% (13/20), 100.0% (15/15). The expression of PGC in gastric carcinoma tis- sues was significantly higher than that in atrophic gastritis tissues (P=0. 000) and normal tissue (P=0. 000), and there was significant different between the latter two groups (P=0. 033). Expression of PGC was significantly correlated with differentiation status (P=0. 037) and clinical stage (P=0. 044) of the cancer (P〈0.05). There was a negative correla- tion between AKT-2 and PGC (r=- 0. 297, P=0.01). CONCLUSIONS: The expression of AKT-2 in gastric carcinomatissues is significantly higher than that carcinoma tissues is significantly lower AKT-2 and the lowexpression of PGC in atrophic gastritis tissues and normal tissue, but the expression of PGC in gastr
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