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On-line Access: 2022-02-17

Received: 2021-04-25

Revision Accepted: 2021-08-30

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Citations:  Bibtex RefMan EndNote GB/T7714

 ORCID:

Yin LI

https://orcid.org/0000-0002-4019-3391

Yi ZHANG

https://orcid.org/0000-0001-5875-6108

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Journal of Zhejiang University SCIENCE B

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Chemerin promotes proliferation and migration of ovarian cancer cells by upregulating expression of PD-L1


Author(s):  Chenxi GAO, Jinming SHI, Jingxin ZHANG, Yin LI, Yi ZHANG

Affiliation(s):  Department of Gynecology, the First Affiliated Hospital of China Medical University, Shenyang 110001, China; more

Corresponding email(s):  syzi@163.com, yinli@bjmu.edu.cn

Key Words:  Ovarian cancer; Intraperitoneal tumor microenvironment; Chemerin; Programmed death ligand 1 (PD-L1)


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Chenxi GAO, Jinming SHI, Jingxin ZHANG, Yin LI, Yi ZHANG. Chemerin promotes proliferation and migration of ovarian cancer cells by upregulating expression of PD-L1[J]. Journal of Zhejiang University Science B,in press.Frontiers of Information Technology & Electronic Engineering,in press.https://doi.org/10.1631/jzus.B2100392

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author="Chenxi GAO, Jinming SHI, Jingxin ZHANG, Yin LI, Yi ZHANG",
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year="in press",
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doi="https://doi.org/10.1631/jzus.B2100392"
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Abstract: 
Ovarian cancer is the third-most-common malignant reproductive tumor in women. According to the American Cancer Society, it has the highest mortality rate of gynecological tumors. The five-year survival rate was only 29% during the period from 1975 to 2008 (Reid et al., 2017). In recent decades, the five-year survival rate of ovarian cancer has remained around 30% despite continuous improvements in surgery, chemotherapy, radiotherapy, and other therapeutic methods. However, because of the particularity of the volume and location of ovarian tissue, the early symptoms of ovarian cancer are hidden, and there is a lack of highly sensitive and specific screening methods. Most patients have advanced metastasis, including abdominal metastasis, when they are diagnosed (Reid et al., 2017). Therefore, exploring the mechanism of ovarian cancer metastasis and finding early preventive measures are key to improving the survival rate and reducing mortality caused by ovarian cancer.

脂肪因子chemerin通过上调PD-L1的表达促进卵巢癌细胞增殖和迁移

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100ng/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。

关键词组:卵巢癌;腹腔肿瘤微环境;脂肪因子;程序性死亡配体-1(PD-L1)

Darkslateblue:Affiliate; Royal Blue:Author; Turquoise:Article

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