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1.
International Eye Science ; (12): 150-152, 2018.
Article in Chinese | WPRIM | ID: wpr-695145

ABSTRACT

AIM:To describe the outcomes of corneal stromal lenticules in repairing of corneal ulcer and/or perforation.METHODS:This was a retrospective chart review of 6 eyes of 6 patients from January to June 2017,who underwent corneal ulcer repair with the corneal,stromal lenticules harvested from femtosecond laser refractive surgery and kept in pure glycerin for use.Three cases of infectious corneal ulcers were bacterial,fungal,and infection with foreign bodies in corneal deep layer,one each.The other 3 were corneal ulcer perforation.Making sure no air bubble between donor graft and Descemet membrane.The mean follow-up time was 3.71 ±1.56mo (range 1-6mo).RESULTS:All eyes were successfully treated under control of infection without intra-operative complications,and early postoperative evaluation showed a clear graft in all cases.The last follow-up visit showed the mean best corrected visual acuity (VA) significantly improved after surgery.There was significant difference from 0.48±0.12 to 1.50±0.08 (P<0.01).CONCLUSION:The preliminary results suggest that the use of corneal stromal lenticules may be a safe and effective surgical alternative for corneal ulcer,even though the long-term outcome of the graft needs to be further observed.

2.
Bulletin of The Academy of Military Medical Sciences ; (6): 61-64,67, 2010.
Article in Chinese | WPRIM | ID: wpr-642261

ABSTRACT

Objective To investigate the expression of Foxp3~+ lymphocytes in breast carcinoma tissues and their correlation with other pathological factors,and to investigate the mechanism of action of Treg cells.Methods The expression of Foxp3~+ lymphocytes in the breast cancer tissue and non-cancerous tissue was detected by flow cytometry (FCM) in 30 breast carcinoma patients, and its correlation with other pathological factors was statistically analyzed by multiple linear regression analysis.The expression of TGF-β and IL-10 in the lymphocytes infiltrated in breast cancer tissue and non-cancerous tissue was measured by immunohistochemistry, and their correlation with the expression of Foxp3~+ lymphocytes was statistically analyzed by linear correlation dependability analysis. Results There was significant difference in the expression of Foxp3~+ lymphocytes between the malignant and non-cancerous breast tissues(P<0.05),and it was positively correlated with the clinical stage,blood vessel invasion and the matter of axillary lymph node metastasis(P<0.05). The expression of IL-10 in the tumor infiltrating lymphocytes was positively correlated with the expression of Foxp3~+ lymphocytes(P<0.05).Conclusion The expression level of Foxp3~+ lymphocytes is correlated with invasion and metastasis of breast carcinoma, and the IL-10 secreted by Foxp3~+ lymphocytes may be involved in this effect.Foxp3~+ lymphocytes can be used as an assistant marker for prediction and new therpeutic target of breast cancer.

3.
Tumor ; (12): 548-551, 2008.
Article in Chinese | WPRIM | ID: wpr-849329

ABSTRACT

Objective: To investigate the effect of spleen tyrosine kinase (Syk) on invasion and migration in human breast cancer cells and analyze its action mechanism. Methods: Full-length cDNA of Syk was transfected into Syk-negative human breast cancer cells MDA-MB-231 via liposome mediation. The invasion and migration ability of MDA-MB-231 cells was detected by Transwell ECM method. The expressions of invasion and migration-related molecule vasculars, endothelial growth factor (VEGF) and matrix metalloproteinaseses-9 (MMP-9), were detected by flow cytometry (FCM) and enzyme-linked immunosorbant assy (ELISA) methods. Results: The number of membrane-passing cells every 5 high power fields was significantly decreased in Syk-transfected MDA-MB-231 cells compared with those transfected with blank vector or without transfection (P < 0.05). The expressions of VEGF and MMP-9 proteins were obviously reduced (P < 0.05). Conclusion: Syk cDNA inhibited the invasion and migration of tumor cells by down-regulating the expressions of VEGF and MMP-9.

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