河北医科大学学报

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miR32通过调控PI3K/Akt信号通路影响骨肉瘤细胞的增殖

  

  1. 1.河北省唐山市工人医院骨三科,河北 唐山 063000;2.河北省唐山市工人医院儿科,河北 唐山 063000;3.河北省唐山市工人医院影像科,河北 唐山 063000
  • 出版日期:2018-05-25 发布日期:2018-05-30
  • 作者简介:刘春杰(1983-),男,河北迁西人,河北省唐山市工人医院主治医师,医学博士研究生,从事骨外科疾病诊治研究。
  • 基金资助:
    唐山市科技计划项目(15130253a)

miR32 affects proliferation of osteosarcoma cells by regulating PI3K/Akt signaling pathway#br#

  1. 1.The Third Department of Orthopedics, Tangshan Gongren Hospital, Hebei Province, Tangshan
    063000, China; 2.Department of Pediatrics, Tangshan Gongren Hospital, Hebei Province,
    Tangshan 063000, China; 3.Department of Medical Image, Tangshan Gongren
    Hospital, Hebei Province, Tangshan 063000, China
  • Online:2018-05-25 Published:2018-05-30

摘要: [摘要]〓
〖HTH〗目的〖HTSS〗〖KG*2〗探讨microRNA32(miR32)在骨肉瘤细胞增殖中的作用及机制。
〖HTH〗方法〖HTSS〗〖KG*2〗应用逆转录聚合酶链反应(reverse transcriptionpolymerase chain reaction,RTPCR)技术检测骨肉瘤组织与正常组织及不同细胞株中miR32的表达情况。采用CCK8方法检测抑制miR32表达对人成骨肉瘤MG63细胞株增殖速率的影响。用荧光素酶实验检测miR32与人第10号染色体缺失的磷酸酶及张力蛋白同源基因(phosphatase and tensin homolog deleted on chromosome ten,PTEN)的3′UTR特异性结合,采用RTPCR和蛋白质免疫印迹技术分别从RNA及蛋白质水平上验证miR32与PTEN的关系。
〖HTH〗结果〖HTSS〗〖KG*2〗miR32在骨肉瘤组织及细胞中通过与PTEN的3′UTR靶向结合后激活了磷脂酰肌醇3激酶/丝氛酸-苏氨酸蛋白激酶(phosphatidylinositol3kinase/serinethreonine kinase,PI3K/Akt)信号通路,进而影响人成骨肉瘤MG63细胞的增殖。
〖HTH〗结论〖HTSS〗〖KG*2〗miR32通过PI3K/Akt信号通路调控骨肉瘤细胞的增殖。

关键词: 骨肉瘤, 细胞增殖, 微RNAs

Abstract: [Abstract] Objective〖HTSS〗〓To find out the function and mechanism of microRNA32(miR32) in osteosarcoma cell proliferation.
〖HTH〗〖WTHZ〗Methods〖HTSS〗〓Reverse transcriptionpolymerase chain reaction(RTPCR) was used to detect the expression of miR32 in osteosarcoma tissues, normal tissues and different cell lines. The effect of inhibiting miR32 expression on the proliferation rate of human osteosarcoma MG63 cell line was detected by CCK8. Luciferase assay showed that miR32 could bind specifically to the 3′UTR of phosphatase and tensin homolog deleted on chromosome ten(PTEN) gene. At the same time, RTPCR and western blotting were used to verify the relationship between miR32 and PTEN from RNA and protein level respectively.
〖HTH〗〖WTHZ〗Results〖HTSS〗〓miR32 in 〖JP2〗osteosarcoma tissues and cells activate PI3K/Akt signaling pathway after binding to PTEN′s〖JP〗 3′UTR, which further influences the proliferation of MG63 cells. 
〖HTH〗〖WTHZ〗Conclusion〖HTSS〗〓miR32 regulates the proliferation of osteosarcoma cells through PI3K/Akt signaling pathway.

Key words: osteosarcoma; cell proliferation, microRNAs