[Study on EB virus infection, LMP1 and Bcl-2 expression in lung cancer patients].

OBJECTIVE: To investigate the Epstein-Barr virus (EBV) infection, the expression of EBV latent membrane protein 1 ( LMPl) and oncogene bcl-2 in lung cancer patients. METHODS: EBERI in 108 cases of lung cancer were detected with in situ hybridization. EBV positive and negative lung cancer tissues were analysed for the expression of LMP1 and Bcl-2 by immnohistochemistry. The average area (AA) and integral optical density (IA) of each sample was measured with the digital medical image analyzing system. RESULTS: In 108 cases of lung cancer, 36 cases were EBER1 positive and 7 cases were LMP1 positive. The expression of Bcl-2 was higher in EBV positive lung cancer tissues than that in EBV negative. The AA value was 58014.23 +/- 6918.45 and 38156.22 +/- 4096.79, while the IA value was 11.00 +/- 1.48 and 8.03 +/- 0.78 respectively. No statistic difference was fund in the expression of Bcl-2 betwen LMP1 positive and negative lung cancer tisssues. CONCLUSION: EBV infection in lung cancer increased the expression of bcl-2, which may play a role in the occurrence or development of lung cancer. The increased expression of Bcl-2 may not be induced by LMP1. The exact mechanism need further study.

[Detection of Epstein-Barr virus in lung carcinoma tissue by in situ hybridization].

OBJECTIVES: To examine the Epstein-Barr virus (EBV) in primary lung carcinoma tissue, and to investigate the relationship between EBV infection and tumorigenesis of lung cancer. METHODS: Formalin-fixed and paraffin-embedded lung tissue specimens from surgically resected lung carcinoma tissues of 108 cases treated in Tanshan area from 2001 to 2006, which were confirmed further by histopathological examination after hematoxylin-eosin (HE) staining, were used to observe the EBV encoded RNA-1 (EBER1) using in situ hybridization (ISH). RESULTS: EBER1 was detected in 36 of the 108 primary lung carcinoma cases, and in 1 of the 22 normal lung tissues. The positive rates of EBV infection in squamous cell carcinoma, adenocarcinoma, small cell carcinoma and large cell carcinoma were 35.9%, 31.6% 31.0%, 1/2, respectively. Gender, age and clinicohistopathological type were not found to have any correlation with EBER1 expression, but EBER1 expression in groups of cases with poorly and moderately differentiated carcinomas was significantly higher than those in the group of cases with well differentiated carcinoma, and the EBER1 expression in the right lung was higher than in the left lung. CONCLUSIONS: The frequency of EBV infection in this series of patients from Tangshan area was 33.3%, the results suggest that there is a relationship between EBV infection and the occurrence of the primary lung carcinoma, EBV infection might be one of the potential causes to induce lung cancer.

[Effect of anthocyanin rich fruit extract on PGE2 produced by endothelial cells].

OBJECTIVE: To study the effect of anthocyanin rich fruit extract on PGE2 produced by endothelial cells. METHODS: Normal human endothelial cells, CRL-2606, were cultured in F12K medium (complemented with 10% FBS, 0.1 mg/ml heparin, 0.03 mg/ml ECGS, 50 microg/ml streptomycin and 500U/ml penicillin) in 5% CO2 with 95% air at 37 degrees C. When the cells grow close to confluence, anthocyanin rich fruit extract with/without 100 ng/ml of LPS were added to the medium. After 18 hours of incubation, cells were harvested and the supernatant were collected. Cell viability was assayed. After centrifugation, PGE2 concentration in the supernatant was measured with the STAT-Prostaglandin E2 EIA Kit. RESULTS: 300 microg/ml or higher Chokeberry extract showed cytotoxicity effect on CRL-2606 cells, the viability was lower than 60% and showed a dose-response manner. Under using dosage, Blackcurrant extract (100 - 700 microg/ml) and Blueberry extract (50 - 400 microg/ml) did not show any cytotoxicity. When stimulated by LPS, the production of PGE2 by endothelial cells were increased two fold. Blueberry extract inhibit such action. 100 microg/ml of Blueberry extract keeps the production of PGE2 in normal level. 700 microg/mL of Blackcurrant extract and 500 microg/ml Chokeberry extract also inhibit the releasing of PGE2. CONCLUSION: Anthocyanin rich fruit extract from Blueberry, Blackcurrant, and Chokeberry inhibit PGE2 produced by endothelial cells, there exist antiinflammation and antioxidation.