通过PI3K/AKT途径调节胶质母细胞瘤CD47表达对肿瘤侵袭性的影响

刘学键, 武霞, 李玉花

刘学键, 武霞, 李玉花. 通过PI3K/AKT途径调节胶质母细胞瘤CD47表达对肿瘤侵袭性的影响[J]. 实用临床医药杂志, 2020, 24(7): 56-61. DOI: 10.7619/jcmp.202007017
引用本文: 刘学键, 武霞, 李玉花. 通过PI3K/AKT途径调节胶质母细胞瘤CD47表达对肿瘤侵袭性的影响[J]. 实用临床医药杂志, 2020, 24(7): 56-61. DOI: 10.7619/jcmp.202007017
LIU Xuejian, WU Xia, LI Yuhua. Influence of CD47 expression regulated by PI3K/AKT pathway on the tumor invasiveness of glioblastoma[J]. Journal of Clinical Medicine in Practice, 2020, 24(7): 56-61. DOI: 10.7619/jcmp.202007017
Citation: LIU Xuejian, WU Xia, LI Yuhua. Influence of CD47 expression regulated by PI3K/AKT pathway on the tumor invasiveness of glioblastoma[J]. Journal of Clinical Medicine in Practice, 2020, 24(7): 56-61. DOI: 10.7619/jcmp.202007017

通过PI3K/AKT途径调节胶质母细胞瘤CD47表达对肿瘤侵袭性的影响

基金项目: 

山东省重点研发计划项目(2018GSF118038)

详细信息
  • 中图分类号: R739.41

Influence of CD47 expression regulated by PI3K/AKT pathway on the tumor invasiveness of glioblastoma

  • 摘要: 目的 探讨通过磷脂酰肌醇3-激酶(PI3K)/蛋白质丝氨酸苏氨酸激酶(AKT)通路调节胶质母细胞瘤CD47表达对肿瘤侵袭性的影响。 方法 选取手术切除并经病理证实的30例胶质母细胞瘤脑组织标本以及10个正常脑组织对照标本。分析低表达及高表达的CD47对胶质母细胞瘤侵袭性的影响。 结果 CD47在胶质母细胞瘤细胞中高表达, CD47低表达显著抑制了肿瘤侵袭性,而CD47的高表达则显著促进肿瘤侵袭性。CD47通过激活PI3K/AKT途径而显著增强胶质母细胞瘤的侵袭性(P<0.05)。 结论 CD47在胶质母细胞瘤细胞中高表达, CD47通过激活PI3K/AKT途径而增强胶质母细胞瘤的侵袭性。
    Abstract: Objective To investigate the effect of CD47 expression regulated by phosphatidylinositol 3-kinase(PI3K)/protein serine threonine kinase(AKT)pathway on the tumor invasiveness of glioblastoma. Methods Thirty samples of glioblastoma brain tissue confirmed by pathology were collected, and 10 normal samples of brain tissues were collected as controls. Effect of low and high expressions of CD47 on the invasiveness of glioblastoma were analyzed. Results CD47 was highly expressed in glioblastoma cells, and low expression of CD47 could significantly inhibit the tumor invasiveness, and high expression of CD47 could significantly promote the tumor invasiveness. CD47 was able to significantly enhance invasiveness of glioblastoma by activating the PI3K/AKT pathway(P<0.05). Conclusion CD47 is highly expressed in glioblastoma cells, and CD47 can significantly enhance invasiveness of glioblastoma by activating the PI3K/AKT pathway.
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