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作 者:郑少伟[1] 钟浩博[1] 缪海雄[1] 刘伟乐[1] 李胜发[1] 陈楚群[1] 孙春汉[1] ZHENG Shaowei ZHONG Haobo MIAO Haixiong LIU Weile LI Shengfa CHEN Chuqun SUN Chunhan(Department of Orthopedic Surgery, Huizhou First People's Hospital, Huizhou 516001, China)
机构地区:[1]惠州市第一人民医院骨科,广东惠州516001
出 处:《分子影像学杂志》2017年第1期40-43,共4页Journal of Molecular Imaging
摘 要:目的探讨p53凋亡刺激蛋白2(ASPP2)对骨肉瘤细胞转移的影响及其机制。方法 Q-PCR检测骨肉瘤组织和细胞中ASPP2 mRNA的表达;western blot检测骨肉瘤细胞中ASPP2蛋白表达;transwell检测细胞转移能力;co-IP实验检测β-catenin和E-cadherin相互作用水平;免疫荧光检测β-catenin在细胞核中表达水平。结果 8例手术标本Q-PCR检测发现,骨肉瘤组织中ASPP2 mRNA的表达较癌旁组织明显降低;4株骨肉瘤细胞系中(OS187、SAOS2、HOS和MG63)ASPP2 mRNA和蛋白的表达较正常成骨细胞明显减少。过表达ASPP2蛋白的SAOS2其转移能力明显减弱,同时β-catenin和E-cadherin相互作用水平增加,而β-catenin核转位减少。结论 ASPP2可以减少骨肉瘤细胞SAOS2的转移,其机制可能的通过稳定β-catenin-E-cadherin复合体,抑制β-catenin核转位。Objective To explore the effect and mechanism of apoptosis stimulating protein2 of p53 (ASPP2) in osteosarcoma cells metastasis. Methods Quantitative-Polymerase Chain Reaction (Q-PCR) was performed to determine ASPP2 mRNA in eight samples of osteosarcoma tissue and four cell lines of osteosarcoma. The levels of ASPP2 protein were detected by western blot. The metastasis ability of SAOS2 cells that overexpressed ASPP2 were estimated by Transwell experiment. The Levels of interaction of β-catenin and E-cadherin were analyze by co-IP. Immunofluorescence was used to detect the expression of ASPP2 protein in the nuclear of osteosarcoma cells. Results The ASPP2 mRNA levels in eight osteosarcoma tissue samples were decreased significantly than that in normal bone tissue. Compared with normal human osteoblast cells HOSB, the levels of BRMS1 mRNA and protein obviously decreased in osteosarcoma cell lines OS187, SAOS2, HOS and MG63. The metastasis ability, β-catenin-E-cadherin complex and β-catenin nuclear-translocation of SAOS2 ceils was significantly inhibited after ASPP2 overexpression. Conclusion BRMS1 can inhibit SAOS2 cells metastasis and the mechanism may involve with stabilizing the β-catenin-E-cadherin complex, and suppress β-catenin nudear-translocation.
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