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胶质瘤U251干细胞通过FOXO3a/β-catenin通路调控TMZ耐药性的研究OACSTPCD

Study on glioma U251 stem cells regulate TMZ drug resistance through FOXO3a/β-catenin pathway

中文摘要英文摘要

目的 探讨胶质瘤U251干细胞是否通过FOXO3a/β-catenin通路调控其对替莫唑胺(TMZ)的耐药性.方法 U251干细胞分为TMZ组(100μmol/L TMZ处理细胞)和对照组,Western blot及实时荧光定量逆转录-PCR(qRT-PCR)实验检测两组TMZ作用下FOXO3a、β-catenin、Nestin、CD133、Sox2表达情况.干细胞成球实验验证U251干细胞对TMZ的耐受情况.将FOXO3a/β-catenin干扰序列嵌入慢病毒pHY-LV-KD1.1表达载体构建重组病毒载体pHY-FOXO3a-KD、pHY-β-catenin-KD并转染U251干细胞,在TMZ作用下检测干细胞克隆球数量的变化,观察敲低FOXO3a、β-catenin对U251干细胞特性及耐药性的影响.结果 Western blot 及 qRT-PCR 结果显示,与对照组比较,TMZ 组 FOXO3a、β-catenin、Nestin、CD133、Sox2 蛋白表达水平升高,Nestin、CD133、Sox2 mRNA表达水平升高(P<0.05).克隆形成实验结果显示,TMZ处理5 d后存活下来的细胞多为干细胞,说明U251干细胞可较好地耐受TMZ.敲低FOXO3a、β-catenin可导致U251干细胞群数量减少,说明其对TMZ耐药性减弱.结论 FOXO3a/β-catenin通路可调控U251干细胞特性及TMZ耐药性.

Objective To explore whether or not the glioma U251 stem cell regulates its resistance to TMZ by the FOXO3a/β-catenin pathway.Methods The U251 stem cells were divided into the TMZ group(100 μmol/IL TMZ treated cells)and the control group.The Western blot and real-time quantitative reverse transcription-PCR(qRT-PCR)were used to detect the expression levels of FOXO3a,β-catenin,Nestin,CD133 and Sox2 under the TMZ action in the two groups.The stem cell pelletization experiment was used to verify the resistance of U251 stem cell on TMZ.Recombinant viral vectors pHY-FOXO3a,pHY-β-catenin-KD and PHy-β-Catenin-KD were constructed by embedding FOXO3a/β-catenin interference sequences into lentivirus pHY-LV-KD1.1 expression vector and transfected into U251 stem cells.The change of stem cell clone pellets number was measured under TMZ action.The effects of knockdown FOXO3a and β-catenin on the characteris-tics and drug resistance of U251 stem cells were observed.Results The Western blot and qRT-PCR results showed that compared with the control group,the expression levels of FOXO3a,β-catenin,Nestin,CD133 and Sox2 protein in the TMZ group were increased,the Nestin,CD133,Sox2 mRNA expression levels were in-creased(P<0.05).The clone formation experiment results showed that the majority of survival cells on 5 d after TMZ treatment were the stem cells,indicating that the U251 stem cells could better tolerate TMZ.Knoc-king down FOXO3a and β-catenin could reduce the U251 stem cell populations number,indicating that its re-sistance to TMZ was weakened.Conclusion The FOXO3a/β-catenin pathway could regulates the characteris-tics of U251 stem cell and TMZ resistance.

王政;周艳玲;许可;莫菁莲

海南医学院生物技术与生物化学实验室,海口 571101海口市第四人民医院儿科,海口 571100海南医学院热带医学院,海口 571101海南省人民医院药学部,海口 570311

临床医学

胶质瘤;U251干细胞;FOXO3a/β-catenin;替莫唑胺;耐药性

glioma;U251 stem cell;FOXO3a/β-catenin;temozolomide;drug resistance

《重庆医学》 2024 (013)

1935-1940 / 6

2021年海南省自然科学基金面上项目(821MS043).

10.3969/j.issn.1671-8348.2024.13.003

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