概要
目的
探究腹腔肿瘤微环境内脂肪因子趋化素 (chemerin) 与程序性死亡配体-1 (PD-L1) 是否存在关联, 及其对卵巢癌细胞系 HO8910 细胞生物学功能的影响.
创新点
首次发现了 chemerin 可以上调卵巢癌细胞 PD-L1 的表达, 促进肿瘤增殖和迁移. 这对进一步研究免疫抑制剂在卵巢癌治疗中的应用、 卵巢癌的早期诊断, 以及血清和腹水中 chemerin 的检测具有一定的指导意义. 此外, chemerin 结合其他脂肪因子是否能成为卵巢癌诊断的标志物, 需进一步的研究证实.
方法
使用酶联免疫吸附剂测定 (ELISA) 检测卵巢癌患者腹水和血清中 chemerin 的含量; 使用免疫组化检测卵巢癌肿瘤组织中 chemerin 和 PD-L1 的表达; 使用免疫印迹法检测卵巢癌组织中 PD-L1 的表达及在 HO8910 和 HO891PM 细胞中 chemerin 表达的差异; 利用浓度分别为 0、 10、 50 和 100 ng/mL 外源性 chemerin 刺激 HO8910 和 HO8910PM 细胞; 使用水溶性四唑 (WST) 检测细胞增殖; 使用划痕实验检测细胞迁移功能; 利用鬼笔环肽荧光染色在共聚焦显微镜下观察 PD-L1 敲除前后的 HO8910 和 HO8910PM 的细胞骨架变化; 使用免疫印迹法检测细胞骨架蛋白的表达情况.
结论
Chemerin 可以上调卵巢癌细胞 PD-L1 的表达, 对肿瘤增殖和迁移具有促进作用.
References
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Acknowledgments
This work was supported by the Special Project for Central Guidance of Local Science and Technology Development of Liaoning Province (No. 2019JH6/10400006), China.
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Chenxi GAO, Jinming SHI, and Jingxin ZHANG performed the experimental research and data analysis, and wrote the manuscript. Yin LI and Yi ZHANG contributed to the study design, data analysis, and writing and editing of the manuscript. All authors have read and approved the final manuscript, and therefore, have full access to all the data in the study and take responsibility for the integrity and security of the data.
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Chenxi GAO, Jinming SHI, Jingxin ZHANG, Yin LI, and Yi ZHANG declare that they have no conflict of interest.
All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2008 (5). Informed consent was obtained from all patients for being included in the study. Additional informed consent was obtained from all patients for whom identifying information is included in this article.
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Gao, C., Shi, J., Zhang, J. et al. Chemerin promotes proliferation and migration of ovarian cancer cells by upregulating expression of PD-L1. J. Zhejiang Univ. Sci. B 23, 164–170 (2022). https://doi.org/10.1631/jzus.B2100392
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DOI: https://doi.org/10.1631/jzus.B2100392