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前列腺素D2调控自噬影响胃癌干细胞的干性

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目的:探究前列腺素D2(Prostaglandins D2,PGD2)对胃癌干细胞(gastric cancer stem cells,GCSCs)干性的影响及机制。方法:通过无血清培养法富集7901-GCSCs;然后通过流式细胞术检测无血清培养的7901-GCSCs干性标志物CD44的阳性率;通过干细胞成球实验检测不同浓度PGD2(2。5、5、10)μg/mL刺激后的成球能力,并采用Western blot实验检测不同浓度PGD2刺激后干性相关指标(OCT4、CD44)和自噬相关蛋白(LC3、Beclin-1)的表达。采用Western blot实验检测不同浓度CQ(2。5、5、10)μmol/L刺激后自噬相关蛋白的表达。通过Western blot实验检测PGD2以及PGD2+CQ处理后自噬相关蛋白(LC3、Beclin-1)和干性相关指标(OCT4、CD44)的蛋白表达。结果:流式细胞术结果显示,与胃癌细胞SGC-7901相比,无血清培养的 7901-GCSCs中CD44 阳性率表达增加(P<0。05)。干细胞成球实验结果表明,与DMSO组相比,PGD2组中7901-GCSCs的成球能力明显减弱(P<0。05)。Western blot结果显示,与DMSO组相比,PGD2组中7901-GCSCs的干性相关指标(OCT4、CD44)蛋白表达下调(P<0。05),而自噬相关蛋白(LC3、Beclin-1)表达增加(P<0。05)。与DMSO组相比,CQ组中自噬相关蛋白(LC3、Beclin-1)表达降低(P<0。05)。Western blot结果还显示,与DMSO组相比,PGD2+CQ组中细胞自噬相关蛋白以及干性相关指标表达并无明显变化,提示CQ可阻断PGD2对7901-GCSCs的干性抑制作用。结论:PGD2可能通过调控自噬影响7901-GCSCs的干性。
Prostaglandin D2 regulation of autophagy affects stemness of gastric cancer stem cells
Objective:To explore the effect and mechanism of prostaglandins D2(PGD2)on the stemness of gastric can-cer stem cells(GCSCs).Methods:7901-GCSCs were enriched by serum-free culture method;then the positivity rate of CD44,a stemness marker,was detected by flow cytometry in serum-free cultured 7901-GCSCs;the sphere-forming ability was detected by the sphere-forming assay after stimulation with different concentrations of PGD2(2.5,5,10)μg/mL,and the expression of stem-ness-related indicators(OCT4,CD44)and autophagy-related proteins(LC3,Beclin-1)after PGD2 stimulation was detected by the Western blot assay in different concentrations.The expression of stemness-related indexes(OCT4,CD44)and autophagy-re-lated proteins(LC3,Beclin-1)were detected by Western blot assay after stimulation with different concentrations of PGD2.The expression of autophagy-related proteins after stimulation with different concentrations of CQ(2.5,5,10)μM was detected by Western blot experiment.The protein expression of autophagy-related proteins(LC3,Beclin-1)and stemness-related indexes(OCT4,CD44)was detected by Western blot experiment after PGD2 as well as PGD2+CQ treatment.Results:Flow cytome-try results showed that the expression of CD44 positivity was increased in serum-free cultured 7901-GCSCs compared with gastric cancer cells SGC-7901(P<0.05),which fulfilled the needs of subsequent experiments.The results of stem cell spheroid forma-tion assay showed that the spheroid formation ability of 7901-GCSCs in the PGD2 group was significantly weakened compared with that of the DMSO group(P<0.05).Western blot results showed that the protein expression of stemness-related indexes(OCT4,CD44)was down-regulated in the 7901-GCSCs in the PGD2 group compared with that of the DMSO group(P<0.05),and the expression of autophagy-related proteins(LC3,Beclin-1)expression increased(P<0.05).Compared with the DMSO group,the expression of autophagy-related proteins(LC3,Beclin-1)was decreased in the CQ group(P<0.05).Western blot re-sults also showed that the expression of cellular autophagy-related proteins and stemness-related indexes in the PGD2+CQ group was not significantly changed compared with that of the DMSO group(ns:the difference was not significant),suggesting that the CQ could block the effect of PGD2 on the expression of stemness markers in 7901-GCSCs.Conclusion:PGD2 may affect the stemness of 7901-GCSCs by regulating autophagy.

PGD2Gastric cancerGastric cancer stem cellsAutophagyStemness

田恒金、汪非凡、高培垚、陈阿敏、王娜、张强

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蚌埠医科大学第一附属医院检验科,安徽 蚌埠 233004

蚌埠医科大学肿瘤基础研究与临床检验诊断重点实验室,安徽 蚌埠 233004

海军军医大学第一附属医院输血科,安徽 蚌埠 233004

PGD2 胃癌 胃癌干细胞 自噬 干性

安徽省自然科学基金面上项目蚌埠医学院科研创新项目

1908085MH258Byycxz21004

2024

海南医学院学报
海南医学院

海南医学院学报

CSTPCD北大核心
影响因子:1.068
ISSN:1007-1237
年,卷(期):2024.30(4)
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