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Correlation of Epstein-Barr virus and its encoded proteins with Helicobacter pylori and expression of c-met and c-myc in gastric carcinoma

机译:胃癌中爱泼斯坦-巴尔病毒及其编码蛋白与幽门螺杆菌的相关性及c-met和c-myc的表达

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摘要

AIM: To investigate the interrelationship of Epstein-Barr virus (EBV) and EBV- encoded proteins with Helicobacter pylori (H pylori) infection and the expression of c-met and c-myc oncogene proteins in gastric carcinoma, and to explore their role in gastric carcinogenesis.METHODS: One hundred and eighty-five gastric carcinoma tissues were detected by polymerase chain reaction (PCR)-Southern blot for EBV genome and in situ hybridization (ISH) for EBV-encoded small RNA 1 (EBER1). Gastric carcinoma with positive EBER1 signals was confirmed EBV-associated gastric carcinoma (EBVaGC). The status of H pylori infection in 185 gastric carcinomas was assessed by rapid urease test and PCR. The samples with positive PCR and urease test were defined as H pylori infection. The expression of c-met and c-myc oncogene proteins in tissues of EBVaGC and matched EBV-negative gastric carcinoma (EBVnGC) were examined by immunohistochemistry. RT-PCR and Southern hybridization were used to detect the expression of nuclear antigens (EBNAs) 1 and 2, latent membrane protein (LMP) 1, early genes BARF1 and BHRF1 in EBVaGC cases.RESULTS: The positive rate of H pylori and EBV in 185 gastric carcinomas was 59.45% (110/185) and 7.03% (13/185) respectively. No difference was found in sex, age, pathological differentiation, clinical stages and lymph node metastasis between H pylori-positive and H pylori-negative gastric carcinomas. However, the positive rate of H pylori infection in the antrum gastric carcinomas was higher than that of cardia and body gastric carcinomas. In our series, age, pathological differentiation, clinical stages, lymph node metastasis and location of cancer were not different between EBVnGC and EBVaGC, while the positive rate of EBV in male patients was significantly higher than that of female patients. The positivity of H pylori in EBV-associated and EBV-negative gastric carcinomas was 46.15% (6/13) and 81.40%(104/172) respectively. There was no significant correlation between EBV and H pylori infection. The c-met overexpression was significantly higher in the EBVaGC group than in the EBVnGC group. However, c-met and c-myc expression did not show significant difference between the two groups. Transcripts of EBNA1 were detected in all 13 EBVaGCs, while both EBNA2 and LMP1 mRNA were not detected. Six of the 13 cases exhibited BARF1 transcripts and 2 exhibited BHRF1 transcripts.CONCLUSION: The positivity of H pylori in EBVnGCs is higher than that of EBVaGCs, but no significant correlation is found between EBV infection and H pylori infection. H pylori-positive gastric carcinoma is predominant in antrum location, while EBVaGC has a tendency of predominance in cardia/body location. EBV infection is associated with c-met abnormal expression but not with c-myc protein in EBVaGC. c-met overexpression is not induced by LMP1. BARF1 and BHRF1 may play important roles in the tumorigenesis of EBVaGC through different pathways.
机译:目的:探讨爱泼斯坦-巴尔病毒(EBV)和EBV编码蛋白与幽门螺杆菌(H pylori)感染的相互关系以及c-met和c-myc癌基因蛋白在胃癌中的表达,并探讨其在胃癌中的作用。方法:通过聚合酶链反应(PCR)-Southern blot检测185份胃癌组织中的EBV基因组,并用原位杂交(ISH)检测EBV编码的小RNA 1(EBER1)。 EBER1信号阳性的胃癌被证实与EBV相关的胃癌(EBVaGC)。通过快速尿素酶试验和PCR评估185例胃癌中幽门螺杆菌感染的状况。 PCR和尿素酶测试阳性的样品被定义为幽门螺杆菌感染。通过免疫组织化学检查了EBVaGC和匹配的EBV阴性胃癌(EBVnGC)组织中c-met和c-myc癌基因蛋白的表达。 RT-PCR和Southern杂交检测EBVaGC病例中核抗原(EBNAs)1、2,潜伏膜蛋白(LMP)1,早期基因BARF1和BHRF1的表达。 185胃癌分别为59.45%(110/185)和7.03%(13/185)。幽门螺杆菌阳性和阴性的胃癌在性别,年龄,病理分化,临床分期和淋巴结转移方面均无差异。然而,胃窦癌中幽门螺杆菌感染的阳性率高于card门癌和人体胃癌。在我们的系列中,EBVnGC和EBVaGC之间的年龄,病理分化,临床分期,淋巴结转移和癌的位置没有差异,而男性患者的EBV阳性率显着高于女性患者。幽门螺杆菌在EBV相关和EBV阴性胃癌中的阳性率分别为46.15%(6/13)和81.40%(104/172)。 EBV与幽门螺杆菌感染之间无显着相关性。 EBVaGC组的c-met过表达明显高于EBVnGC组。但是,c-met和c-myc的表达在两组之间没有显着差异。在所有13个EBVaGC中均检测到EBNA1转录本,而未检测到EBNA2和LMP1 mRNA。结论:13例中有6例表现出BARF1转录本,2例表现出BHRF1转录本。结论:EBVnGCs中幽门螺杆菌的阳性率高于EBVaGCs,但EBV感染与Hpylori感染之间无显着相关性。幽门螺杆菌阳性胃癌在胃窦部位占主导地位,而EBVaGC在心脏/身体部位占主导地位。 EBV感染与EBVaGC中c-met异常表达有关,但与c-myc蛋白无关。 LMP1不会诱导c-met过表达。 BARF1和BHRF1可能通过不同途径在EBVaGC的肿瘤发生中发挥重要作用。

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