VEGF与肿瘤血管生成拟态关系的研究(英文)

来源 :Chinese-German Journal of Clinical Oncology | 被引量 : 0次 | 上传用户:haohade
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Objective: The aim of this study was to explore the relationship between VEGF expression and vasculogenic mimicry of tumor in vitro. Methods: We observed the ability to form vasculogenic mimicry in several cell lines follow as LO2 cell, hepG2 cell, SMMC-7721 cell and A549 cell in three-dimensional cultures; we detected the expression of VEGF in the level of mRNA and protein by polymerase chain reaction (PCR) and western blot in those cell lines. Results: HepG2 cell and A549 cell had the ability to form vasculogenic mimicry in three-dimensional cell cultures, while LO2 cell and SMMC-7721 cell hadn’t the ability. The rates of VEGF165/GAPDH were 0.212 ± 0.011,0.208 ± 0.013, 0.117 ± 0.009 and 0.214 ± 0.012 respectively, and the rates of VEGF121/GAPDH were 0.186 ± 0.018, 0.192 ± 0.014, 0.050 ± 0.010, 0.196 ± 0.017 in LO2 cell, hepG2 cell, SMMC-7721 cell and A549 cell, separately. The expression of VEGF gene in mRNA and protein levels in HepG2 cell, LO2 cell and A549 cell were significantly higher than that in SMMC-7721 cell (P < 0.05). Conclusion: The cell lines which the expression of VEGF gene is low don’t have the ability to form vasculogenic mimicry and the high expression of VEGF gene cann’ t form vasculogenic mimicry at all, while the expression of VEGF gene in the cell lines is high in the cell lines which can form vasculogenic mimicry. VEGF has impact on the formation vasculgenic mimicry. Only the cells which the expression of VEGF is high have the potential to form vasculogenic mimicry. But, it doesn’t play a unique key role in vasculogenic mimicry. Objective: The aim of this study was to explore the relationship between VEGF expression and vasculogenic mimicry of tumor in vitro. Methods: We observed the ability to form vasculogenic mimicry in several cell lines follow as LO2 cell, hepG2 cell, SMMC-7721 cell and A549 cell in three-dimensional cultures; we detected the expression of VEGF in the level of mRNA and protein by polymerase chain reaction (PCR) and western blot in those cell lines. Results: HepG2 cell and A549 cell had the ability to form vasculogenic mimicry in rates of VEGF165 / GAPDH were 0.212 ± 0.011, 0.208 ± 0.013, 0.117 ± 0.009 and 0.214 ± 0.012 respectively, and the rates of VEGF121 / GAPDH were 0.186 ± 0.018, 0.192 ± 0.014, 0.050 ± 0.010, 0.196 ± 0.017 in LO2 cells, hepG2 cells, SMMC-7721 cells and A549 cells, respectively. The expression of VEGF gene in mRNA and protein levels in HepG2 cells, LO2 cell and A549 cell were sign ificantly higher than that in SMMC-7721 cells (P <0.05). Conclusion: The cell lines which the expression of VEGF gene is low do not have the ability to form vasculogenic mimicry and the high expression of VEGF gene cann ’t form vasculogenic mimicry at all, while the expression of VEGF gene in the cell lines is high in the cell lines which can form vasculogenic mimicry. VEGF has impact on the formation vasculgenic mimicry. Only the cells which the expression of VEGF is high have the potential to form vasculogenic mimicry. But, it does not play a unique key role in vasculogenic mimicry.
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