| 注册
首页|期刊导航|空军军医大学学报|PRMT5调控m6A修饰介导三阴性乳腺癌细胞对多柔比星敏感性的机制研究

PRMT5调控m6A修饰介导三阴性乳腺癌细胞对多柔比星敏感性的机制研究

樊聪 汪家佳 王廷 张健

空军军医大学学报2024,Vol.45Issue(7):788-795,8.
空军军医大学学报2024,Vol.45Issue(7):788-795,8.DOI:10.13276/j.issn.2097-1656.2024.07.011

PRMT5调控m6A修饰介导三阴性乳腺癌细胞对多柔比星敏感性的机制研究

Mechanism research of PRMT5 regulating m6A modification to mediate sensitivity of triple-negative breast cancer cells to doxorubicin

樊聪 1汪家佳 2王廷 1张健2

作者信息

  • 1. 空军军医大学西京医院甲状腺乳腺血管外科,陕西西安 710032
  • 2. 空军军医大学西京医院消化系肿瘤整合防治全国重点实验室,空军军医大学基础医学院生物化学与分子生物学教研室,陕西西安 710032
  • 折叠

摘要

Abstract

Objective To explore the molecular mechanism of protein arginine methyltransferases 5(PRMT5)reducing the sensitivity of triple-negative breast cancer cells to doxorubicin(DOX)by regulating RNA m6A modification.Methods The TCGA database was used to analyze the expression level of PRMT5 in breast cancer tissues and its correlation with prognosis of patients.Human breast cancer MDA-MB-231 cell lines with stable overexpression and knockdown of PRMT5 were constructed.The effect of PRMT5 on DOX sensitivity of breast cancer cells was analyzed by CCK-8 and colony formation assay.The effect of PRMT5 on the expression level of m6A-related molecules in MDA-MB-231 cells under DOX was detected by qRT-PCR and Western blotting.MeRIP-seq was used to analyze the target genes with significant differences in m6A modification under the regulation of DOX by PRMT5,and the expression level and RNA stability of the target genes were detected through qRT-PCR.Results The results of TCGA database analysis showed that PRMT5 was highly expressed in breast cancer and other various tumors(P<0.05),and high expression of PRMT5 predicted poor prognosis.Overexpression of PRMT5 reduced the sensitivity of MDA-MB-231 cells to DOX(P<0.01),while knockdown of PRMT5 or using PRMT5 inhibitor JNJ significantly increased it(P<0.01,P<0.05).Overexpression of PRMT5 notably inhibited the increase of m6A levels in cells induced by DOX(P<0.01),particularly reduced the RNA methylation levels of molecules associated with DNA damage,such as ERCC4 and REV3L,and promoted RNA stability of these molecules.Conclusion PRMT5 reduces RNA methylation level of molecules related to DNA damage repair in MDA-MB-231 cells to increase its stability,thereby reducing the cell sensitivity to DOX.

关键词

PRMT5/m6A/乳腺癌/多柔比星

Key words

PRMT5/m6A/breast cancer/doxorubicin

分类

医药卫生

引用本文复制引用

樊聪,汪家佳,王廷,张健..PRMT5调控m6A修饰介导三阴性乳腺癌细胞对多柔比星敏感性的机制研究[J].空军军医大学学报,2024,45(7):788-795,8.

基金项目

国家自然科学基金面上项目(82073202) (82073202)

陕西省创新人才推进计划-科技创新团队项目(2023-CX-TD-67) (2023-CX-TD-67)

空军军医大学西京医院学科助推计划项目(XJZT24CY53,XJZT24JC17) (XJZT24CY53,XJZT24JC17)

空军军医大学学报

OACHSSCD

2097-1656

访问量0
|
下载量0
段落导航相关论文