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尼拉帕利的联合使用增强了抗GD2抗体对骨肉瘤细胞的抑制作用。

Combined use of niraparib enhanced the inhibitory effect of Anti-GD2 antibody on osteosarcoma cells.

作者信息

Wenyao Chen, Shuai Ma, Yifeng Fan, Xinzhi Li, Xiangyong Que

机构信息

Affiliated Renhe Hospital of China Three Gorges University, No. 410, Yiling Avenue, Yichang, 443001, China.

出版信息

Discov Oncol. 2024 Jul 24;15(1):304. doi: 10.1007/s12672-024-01166-y.

DOI:10.1007/s12672-024-01166-y
PMID:39048747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11269552/
Abstract

PURPOSE

This study aims to investigate the effect of Niraparib in combination with an Anti-GD2 Antibody on osteosarcoma cells.

METHODS

Scratch test was utilized to assess cell migration capacity, while the Transwell experiment was utilized to evaluate cell invasion potential. Cell proliferation was measured using the CCK8 experiment. The affinity between the anti-GD2 antibody and its antigen was determined via ELISA. Tumor growth was evaluated through animal experiments. Western blotting, QRT-PCR, and histological analysis were conducted to examine the expression of relevant proteins and mRNAs.

RESULTS

MG63 cell line was used for an example. The scratch test showed that the migration rate of osteosarcoma cells in Niraparib + Anti-GD2 group was 1.07 ± 0.04 after 48 h, and 0.34 ± 0.04 in the Control group. Transwell experiment showed that the invasion ability of osteosarcoma cells in Niraparib + Anti-GD2 group was 21.0 ± 1.5, and that in Control group was 87.7 ± 2.9. CCK8 experiment showed that the absorbance value of Niraparib + Anti-GD2 group was 0.16 ± 0.10 on day 5, and that of the Control group was 0.76 ± 0.09. Western blotting showed that the expression levels of BALP and CICP in Niraparib + Anti-GD2 group were 0.751 ± 0.135 and 1.086 ± 0.115, respectively, and those in Control group were 1.025 ± 0.143 and 1.216 ± 0.168, respectively. QRT-PCR results showed that the absorbance values of Niraparib + Anti-GD2 group were 0.173 ± 0.065 and 0.170 ± 0.078 on day 14. The results of animal experiments showed that on day 5, the tumor volume of the Control group was 2433 ± 391, and that of the Niraparib + Anti-GD2 group was 1137 ± 148. Histological analysis showed that the mean density values of Niraparib + Anti-GD2 group were 0.19 ± 0.08 and 0.22 ± 0.07, and those of Control group were 0.26 ± 0.09 and 0.29 ± 0.10.

CONCLUSION

The combination of Niraparib and Anti-GD2 antibody significantly inhibits Osteosarcoma cells.

摘要

目的

本研究旨在探讨尼拉帕利与抗GD2抗体联合应用对骨肉瘤细胞的影响。

方法

采用划痕试验评估细胞迁移能力,采用Transwell实验评估细胞侵袭潜能。使用CCK8实验检测细胞增殖情况。通过ELISA测定抗GD2抗体与其抗原之间的亲和力。通过动物实验评估肿瘤生长情况。进行蛋白质免疫印迹法、定量逆转录聚合酶链反应和组织学分析,以检测相关蛋白质和信使核糖核酸的表达。

结果

以MG63细胞系为例。划痕试验显示,尼拉帕利+抗GD2组骨肉瘤细胞在48小时后的迁移率为1.07±0.04,对照组为0.34±0.04。Transwell实验显示,尼拉帕利+抗GD2组骨肉瘤细胞的侵袭能力为21.0±1.5,对照组为87.7±2.9。CCK8实验显示,尼拉帕利+抗GD2组在第5天的吸光度值为0.16±0.10,对照组为0.76±0.09。蛋白质免疫印迹法显示,尼拉帕利+抗GD2组骨碱性磷酸酶和骨钙素的表达水平分别为0.751±0.135和1.086±0.115,对照组分别为1.025±0.143和1.216±0.168。定量逆转录聚合酶链反应结果显示,尼拉帕利+抗GD2组在第14天的吸光度值分别为0.173±0.065和0.170±0.078。动物实验结果显示,在第5天,对照组的肿瘤体积为2433±391,尼拉帕利+抗GD2组为1137±148。组织学分析显示,尼拉帕利+抗GD2组的平均密度值分别为0.19±0.08和0.22±0.07,对照组分别为0.26±0.09和0.29±0.10。

结论

尼拉帕利与抗GD2抗体联合应用可显著抑制骨肉瘤细胞。

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