骨桥蛋白通过LGALS3BP调控PI3K/AKT通路促进肝癌细胞迁移
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内蒙古医科大学基础医学院

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国家自然科学基金项目(面上项目,重点项目,重大项目)


Osteopontin (OPN) activates the PI3K/AKT pathway via upregulating LGALS3BP in promotion of hepatoma cell migration
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College of Basic Medicine, Inner Mongolia Medical University

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The National Natural Science Foundation of China (General Program, Key Program, Major Research Plan)

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    摘要:

    摘要:目的 探讨骨桥蛋白(OPN)通过半乳糖凝集素3结合蛋白(LGALS3BP)促进肝癌细胞迁移的作用及机制。 方法 体外培养人肝癌细胞系SMMC-7721、稳定转染空真核表达载体的人肝癌细胞系SMMC-P及稳定转染OPN基因的人肝癌细胞系SMMC-OPN。qRT-PCR检测细胞中OPN及LGALS3BP mRNA表达情况,Western blot检测细胞中OPN、LGALS3BP和PI3K/AKT通路蛋白表达水平,细胞划痕实验检测细胞迁移能力。SMMC-OPN细胞中分别转染靶向LGALS3BP的小干扰RNA (si-LGALS3BP)及阴性对照(si-NC)后,检测细胞迁移能力变化和PI3K/AKT通路蛋白相对表达水平变化。 结果 相较于亲本细胞SMMC-7721和转染空载体的细胞SMMC-P细胞,高表达OPN的SMMC-OPN细胞迁移能力明显增强,而且细胞中LGALS3BP mRNA及蛋白表达水平显著上调,同时p-PI3K/PI3K及p-AKT/AKT 蛋白相对表达量均显著升高。沉默LGALS3BP表达后,SMMC-OPN细胞的迁移能力受到明显抑制,同时p-PI3K/PI3K及p-AKT/AKT蛋白相对表达水平均显著降低。结论 OPN可以通过上调LGALS3BP的表达激活PI3K/AKT通路,从而促进肝癌细胞迁移。

    Abstract:

    Abstract: Objective To investigate the effect and mechanism of osteopontin (OPN) on hepatoma cell migration through galectin 3 binding protein (LGALS3BP). Methods Human hepatoma cell lines SMMC-7721, SMMC-P (stably transfected with empty eukaryotic expression vectors) and SMMC-OPN (stably transfected with OPN gene) were cultured. The mRNA expression levels of OPN and LGALS3BP were detected by qRT-PCR. Western blot assay was used to analyze the relative expressions of OPN and LGALS3BP. The protein expression level of PI3K/AKT pathway, including p-PI3K, PI3K, p-AKT and AKT were detected by western blot. Wound healing assay was performed to explore the cell migration ability. After transfection with LGALS3BP-targeting small interfering RNA (si-LGALS3BP) and negative control small RNA (si-NC) into SMMC-OPN cells respectively, cell migration ability and the relative expression of PI3K/AKT pathway related proteins were detected. Results Compared with SMMC-7721 and SMMC-P, the migration ability of SMMC-OPN cells was significantly reinforced, and the expression of LGALS3BP was obviously up-regulated at both mRNA and protein. Meanwhile, the relative expression quantity of p-PI3K/PI3K and p-AKT/AKT proteins were significantly increased. Wound healing assay showed that the si-LGALS3BP could obviously suppress the migration ability of SMMC-OPN cells. Furthermore, the relative expression of p-AKT/AKT and p-PI3K/PI3K proteins in SMMC-OPN cells were significantly decreased after transfection with si-LGALS3BP. Conclusion OPN could activate PI3K/AKT pathway through up-regulating LGALS3BP expression in promoting hepatoma cells migration.

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  • 收稿日期:2023-04-28
  • 最后修改日期:2023-05-18
  • 录用日期:2023-12-01
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