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1.
Chinese Medical Journal ; (24): 1989-1994, 2010.
Article in English | WPRIM | ID: wpr-352524

ABSTRACT

<p><b>BACKGROUND</b>Estrogen receptor (ER)-negative breast cancer cells are more aggressive than ER-positive cells. Elevated levels of cyclooxygenase-2 (COX-2) and vascular endothelial growth factor-C (VEGF-C) expression have been detected in cultured human breast cancer cells and are associated with negative hormone receptor status. In this study, we created ERalpha stable transfectants in MDA-MB-231 cells to explore the effect of ERalpha on cell growth and COX-2 and VEGF-C expression.</p><p><b>METHODS</b>The green fluorescent protein (GFP)-ERalpha plasmids were stably transfected into ER-negative MDA-MB-231 cells. The proliferation and migration of untransfected MDA-MB-231 cells, ERalpha-transfected MDA-MB-231 cells and ER-positive MCF-7 cells were determined. The expression of COX-2, and the levels of VEGF-C mRNA and the VEGF-C secretion concentration were assayed in these cell lines.</p><p><b>RESULTS</b>The proliferation and migration capacities of ERalpha-tranfected MDA-MB-231 cells were significantly decreased (P < 0.05). The expression of COX-2 was significantly lower in ERalpha-tranfected MDA-MB-231 cells than in untranfected MDA-MB-231 cells. The mRNA and protein levels of VEGF-C were lower in ERalpha-tranfected MDA-MB-231 cells than in untransfected MDA-MB-231 cells (P < 0.05).</p><p><b>CONCLUSIONS</b>ERalpha stable transfection inhibits proliferation and migration capacities of MDA-MB-231 cells and decreases expression of COX-2 and VEGF-C. The decreases of proliferation and migration capacities may be related to suppression of COX-2 and VEGF-C expression.</p>


Subject(s)
Female , Humans , Blotting, Western , Breast Neoplasms , Genetics , Metabolism , Cell Cycle , Genetics , Physiology , Cell Line, Tumor , Cell Movement , Genetics , Physiology , Cell Proliferation , Cyclooxygenase 2 , Genetics , Metabolism , Enzyme-Linked Immunosorbent Assay , Estrogen Receptor alpha , Genetics , Metabolism , Flow Cytometry , Polymerase Chain Reaction , Transfection , Vascular Endothelial Growth Factor C , Genetics , Metabolism
2.
Journal of Southern Medical University ; (12): 2187-2190, 2009.
Article in Chinese | WPRIM | ID: wpr-325151

ABSTRACT

<p><b>OBJECTIVE</b>To construct a RNA interference expression vector targeting human telomerase reverse transcriptase gene (hTERT) gene and investigate its effects on telomerase activity and proliferation in breast cancer cells in vitro.</p><p><b>METHODS</b>The shRNA sequences targeting hTERT gene were designed and recombined into pSuper-retro-puro vector. The breast cancer cell lines MCF-7 and MDA-MB231 were transfected with the recombined vector, and the telomerase activity of the cells was tested by telomerase repeat sequence amplification-enzyme linked immunosorbent assay (TRAP-ELISA). The proliferation of the transfected cells was assessed using MTT and soft-agar clone formation assays.</p><p><b>RESULTS</b>The recombinant plasmids pSuper-retro-puro-TERT RNAi#1 and #2 were successfully constructed as confirmed by enzymatic digestion and DNA sequencing. The telomerase activity in the transfected breast cancer cells were down-regulated significantly as compared with that in negative control cells (Plt;0.005). The transfection resulted in significant inhibition of the proliferation of both MCF-7 and MDA-MB231 cells as detected by MTT assay (Plt;0.05) and soft agar clone formation assay (Plt;0.001).</p><p><b>CONCLUSION</b>Transfection with the recombinant plasmid containing the shRNA targeting hTERT gene can down-regulate telomerase activity and inhibit proliferation of breast cancer cells in vitro, suggesting the potential of gene therapy targeting telomerase in the treatment of breast cancer.</p>


Subject(s)
Female , Humans , Breast Neoplasms , Genetics , Metabolism , Cell Line, Tumor , Cell Proliferation , Genetic Therapy , Genetic Vectors , Genetics , RNA Interference , RNA, Messenger , Genetics , RNA, Small Interfering , Genetics , Metabolism , Telomerase , Genetics , Metabolism , Transfection
3.
Journal of Southern Medical University ; (12): 2041-2043, 2008.
Article in Chinese | WPRIM | ID: wpr-321761

ABSTRACT

<p><b>OBJECTIVE</b>To observe mid- and long-term changes in the histopathology and electron microscopic characteristics of the acellular dermal matrix engrafted with thin split-thickness skin autograft.</p><p><b>METHODS</b>Twenty-three biopsy samples were collected from 17 patients undergoing extremity scar resection, who received subsequent grafting using allogenic dermal matrix dressed with thin split-thickness skin autografts. Six months to 2 years after the grafting, the grafts were sampled for histopathological and electron microscopic observations of the layer of the epidermis, thickness of the basal membrane, structural components of the dermis, and infiltration of fibroblasts and revascularization. The data were compared with those of the normal skin samples from the patients.</p><p><b>RESULTS</b>Only the number of epidermal layers showed statistically significant difference between the skin grafts and the normal skin (16.33-/+5.89 vs 26.57-/+3.46, P=0.007). The thickness of the basal membrane of the skin grafts was similar to that of normal skin, and no significant difference was found in the number of fibroblasts and newly generated capillaries between them.</p><p><b>CONCLUSION</b>The mid- and long-term histopathology and ultrastructures of the composite skin graft in the extremities are similar to those of normal skin, suggesting satisfactory effect of the skin grafts.</p>


Subject(s)
Adolescent , Child , Child, Preschool , Female , Humans , Male , Burns , General Surgery , Cicatrix , General Surgery , Dermis , Transplantation , Follow-Up Studies , Graft Survival , Skin , Skin Transplantation , Methods , Skin, Artificial , Transplantation, Autologous
4.
Chinese Journal of Plastic Surgery ; (6): 183-185, 2006.
Article in Chinese | WPRIM | ID: wpr-240358

ABSTRACT

<p><b>OBJECTIVE</b>This study was to investigate an operation, in which removing breast cysts of foreign body resulted from augmentation with polyacrylamide hydrogel injection was performed simultaneously with silicone prosthesis implantation under SEPS endoscope in order to relieve tissue injury and increase the accuracy of clearance.</p><p><b>METHODS</b>Eight patients were included in this study. Preoperative type B ultrasound examination was performed to mark the mass. Through an axillary approach, the cysts of foreign body that were distributed in the subcutaneous tissue, breast or muscle were separated and ablated under SEPS endoscope. After removal of the foreign body, a silicone implant was located submuscularly for breast augmentation.</p><p><b>RESULTS</b>The operations were completed without hematoma and infection. Follow-up of the eight patients for 3 to 12 months showed that preoperative symptoms relating to the injected material, such as breast pain, lump and asymmetry, have no longer existed. The shapes of the breasts were satisfactory.</p><p><b>CONCLUSIONS</b>We believe that endoscope-assisted mammoplasty offers more satisfactory clinical results with less injury, less morbidity, less scars, more accuracy and greater patient acceptance.</p>


Subject(s)
Adult , Female , Humans , Young Adult , Acrylic Resins , Breast Implantation , Methods , Breast Implants , Endoscopy , Follow-Up Studies , Foreign Bodies , Mammaplasty , Methods , Silicone Gels , Treatment Outcome
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