首页|肺腺癌长链非编码RNA表皮生长因子受体-反义RNA 1的表达水平与表皮生长因子受体-酪氨酸激酶抑制剂治疗有效率及预后的关系

肺腺癌长链非编码RNA表皮生长因子受体-反义RNA 1的表达水平与表皮生长因子受体-酪氨酸激酶抑制剂治疗有效率及预后的关系

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目的 探讨长链非编码RNA(lncRNA)表皮生长因子受体(EGFR)-反义RNA1(AS1)的表达水平与EGFR-酪氨酸激酶抑制剂(TKI)治疗有效率及预后的关系.方法 采用实时荧光定量聚合酶链反应(PCR)法检测并比较80例肺腺癌患者的肺腺癌组织和癌旁组织、3组转染PC9细胞(control组、pcDNA3.1-NC组、pcDNA3.1-EGFR-AS1组)、PC9细胞和PC9/GR细胞经吉非替尼培养后lncRNA EGFR-AS1的表达水平,采用四甲基偶氮唑蓝(MTT)法和细胞划痕实验分别检测3组转染PC9细胞的活力和迁移能力.以lncRNAEGFR-AS1表达水平的中位数为分界将肺腺癌患者分为lncRNAEGFR-AS1高表达组和低表达组,比较lncRNAEGFR-AS1高、低表达组患者EGFR-TKI治疗的效果及临床特征、生存情况.采用Cox回归法分析肺腺癌患者预后的影响因素.结果 肺腺癌组织和经吉非替尼培养后PC9/GR细胞中lncRNAEGFR-AS1表达水平分别高于癌旁组织和PC9细胞,差异均有统计学意义(P<0.05).lncRNAEGFR-AS1低表达组患者EGFR-TKI治疗总有效率和中位生存时间均明显高于lncRNAEGFR-AS1高表达组患者,差异均有统计学意义(P<0.01).lncRNAEGFR-AS1高、低表达组患者TNM分期、分化程度、淋巴结转移情况、美国东部肿瘤协作组(ECOG)体力状况评分比较,差异均有统计学意义(P<0.05).多因素Cox分析结果显示,TNM分期为Ⅲ~Ⅳ期、lncRNAEGFR-AS1高表达均是肺腺癌患者预后不良的危险因素(P<0.05).pcDNA3.1-EGFR-AS1组PC9细胞中lncRNA EGFR-AS1表达水平、细胞存活率及细胞迁移率均高于control组和pcDNA3.1-NC组,差异均有统计学意义(P<0.05).结论 lncRNAEGFR-AS1参与肺腺癌的发生发展,并且影响患者的预后和EGFR-TKI治疗的有效率.
Relationship between the expression level of long non-coding RNA epidermal growth factor receptor-antisense RNA 1 in lung adenocarcinoma and the therapeutic efficacy and prognosis of epidermal growth factor receptor-tyrosine kinase inhibitor
Objective To investigate the relationship between the expression level of long non-coding RNA(ln-cRNA)epidermal growth factor receptor(EGFR)-antisense RNA 1(AS1)in lung adenocarcinoma and the therapeutic ef-ficacy and prognosis of EGFR-tyrosine kinase inhibitor(TKI).Method Real time fluorescence quantitative polymerase chain reaction(PCR)was used to detect and compare the expression levels of lncRNA EGFR-AS1 in lung adenocarcino-ma tissues and paracancer tissues of 80 lung adenocarcinoma patients,three groups of transfected PC9 cells(control group,pcDNA3.1-NC group,pcDNA3.1-EGFR-ASl group),PC9 and PC9/GR cells cultured with gefitinib.The viability and migration ability of cells in three groups of transfected PC9 cells were detected by methyl thiazolyl terazolium(MTT)and cell scratch assay,respectively.Lung adenocarcinoma patients were divided into lncRNA EGFR-AS1 high expression group and lncRNA EGFR-AS1 low expression group according to the median expression level of lncRNA EGFR-AS1.The effect of EGFR-TKI treatment,the relationship expression level of lncRNA EGFR-AS1 and clinical characteristics,the survival were compared between the lncRNA EGFR-AS1 high and low expression groups.Cox regression was used to analyze the prognostic factors of lung adenocarcinoma patients.Result The expression levels of lncRNA EGFR-AS1 in lung adenocarcinoma tissues and PC9/GR cells cultured by gefitinib were higher than those in paracancer tissues and PC9 cells,and the differences were statistically significant(P<0.05).The total effective rate and median survival time of EGFR-TKI treatment in lncRNA EGFR-AS1 low expression group were significantly higher than those in lncRNA EGFR-AS1 high expression group,and the differences were statistically significant(P<0.01).The TNM stage,differentiation de-gree,lymph node metastasis,and Eastern Cooperative Oncology Group(ECOG)performance status score in lncRNA EG-FR-AS1 high and low expression groups were compared,and the differences were statistically significant(P<0.05).The results of multivariate Cox analysis showed that TNM stage Ⅲ-Ⅳ and high expression of lncRNA EGFR-AS1 were risk factors for poor prognosis in lung adenocarcinoma patients(P<0.05).The expression level of lncRNA EGFR-AS1,cell survival rate and migration rate in PC9 cells of the pcDNA3.1-EGFR-AS1 group were higher than those in control group and pcDNA3.1-NC group,and the differences were statistically significant(P<0.05).Conclusion lncRNA EGFR-AS1 is involved in the occurrence and development of lung adenocarcinoma,and affects the prognosis of patients and the effec-tiveness of EGFR-TKI treatment.

lung adenocarcinomaepidermal growth factor receptorantisense RNA 1tyrosine kinase inhibitor

李肖芸、方家远、李格、周炎峰、宋华勇

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河南大学第一附属医院肿瘤科,河南开封 475000

肺腺癌 表皮生长因子受体 反义RNA1 酪氨酸激酶抑制剂

河南省医学科技攻关计划联合共建项目(2020)

LHGJ20200539

2024

癌症进展
中国医学科学院,北京协和医学院

癌症进展

影响因子:1.004
ISSN:1672-1535
年,卷(期):2024.22(7)