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糖基化磷脂酰肌醇锚定高密度脂蛋白结合蛋白1对胶质瘤生长及巨噬细胞浸润的影响

Effects of glycosylphosphatidylinositol-anchored HDL-binding protein on glioma growth and macrophage infiltration

    摘要
  • 摘要:
    目的 探讨糖基化磷脂酰肌醇锚定高密度脂蛋白结合蛋白1 (GPIHBP1)对胶质瘤生长及巨噬细胞浸润的影响。
    方法 首先，利用TCGA数据库分析人GPIHBP1在胶质瘤样本中的表达及巨噬细胞浸润情况，并在临床组织样本中验证上述生物信息学分析结果; 通过构建稳定过表达GPIHBP1的胶质瘤细胞系，进一步探讨GPIHBP1过表达对胶质瘤细胞增殖、凋亡、迁移和侵袭的影响。最后，通过荷瘤实验验证GPIHBP1过表达对肿瘤生长及巨噬细胞浸润的影响。
    结果 TCGA数据库分析显示, GPIHBP1在低级别胶质瘤中的表达高于正常组织，在高级别胶质瘤中的表达低于正常组织。此外，低级别胶质瘤中GPIHBP1的表达水平高于高级别胶质瘤，这一结果通过免疫组织化学(IHC)实验得到验证。Western blot分析验证了过表达GPIHBP1的胶质瘤细胞系构建成功。CCK-8、流式细胞术、划痕实验和Transwell实验结果显示，该稳转细胞株的增殖能力减弱，迁移能力和侵袭能力降低。荷瘤实验进一步表明，该稳转细胞株的肿瘤生长能力降低，巨噬细胞浸润减少。
    结论 GPIHBP1在不同分级胶质瘤中的表达差异可能与肿瘤进展相关。过表达GPIHBP1可抑制胶质瘤生长，其可能是通过影响肿瘤微环境，促进巨噬细胞向具有抗肿瘤作用的M1型极化，进而抑制胶质瘤生长。

     

    Abstract:
    Objective To investigate the effects of glycosylphosphatidylinositol-anchored HDL-binding protein (GPIHBP1) on glioma growth and macrophage infiltration.
    Methods Initially, the expression of GPIHBP1 in glioma samples and macrophage infiltration were analyzed using TCGA database, and these bioinformatics results were validated in clinical tissue samples. A stable glioma cell line overexpressing GPIHBP1 was then established to further explore the effects of GPIHBP1 overexpression on glioma cell proliferation, apoptosis, migration, and invasion. Finally, the impact of GPIHBP1 overexpression on tumor growth and macrophage infiltration was verified through xenograft experiments.
    Results TCGA database analysis revealed that GPIHBP1 expression was higher in low-grade gliomas compared to normal tissues, while it was lower in high-grade gliomas. Additionally, the expression level of GPIHBP1 in low-grade gliomas was higher than in high-grade gliomas, which was confirmed by immunohistochemistry (IHC). Western blot analysis confirmed the successful construction of the GPIHBP1-overexpressing glioma cell line. CCK-8, flow cytometry, scratch and Transwell assays demonstrated that the proliferation, migration and invasion capabilities of the stable cell line were reduced compared to the control group. Xenograft experiments further showed that the tumor growth and macrophage infiltration were decreased in the stable cell line.
    Conclusion The differential expression of GPIHBP1 in different grades of gliomas may be associated with tumor progression. Overexpression of GPIHBP1 can inhibit glioma growth, possibly by influencing the tumor microenvironment and promoting the polarization of macrophages towards the antitumor M1 phenotype, thereby inhibiting glioma growth.

     

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