首页|miR-214-3p在乳腺癌中的表达模式对铁死亡的影响及其与临床病理特征的关联性研究

miR-214-3p在乳腺癌中的表达模式对铁死亡的影响及其与临床病理特征的关联性研究

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目的 探讨miR-214-3p在乳腺癌中的表达模式对铁死亡的影响及其与临床病理特征的关联性研究.方法 选择2020年2月至2023年3月于南京医科大学康达学院附属连云港东方医院收治的144例乳腺癌患者为研究对象,分析miR-214-3p表达水平与临床特征的关系;采用分层回归模型分析不同临床特征与miR-214-3p表达的关系;另根据患者预后分为死亡组(n=50)和生存组(n=94),比较两组患者的一般资料及铁死亡相关指标,通过Logistic回归分析并构建校正模型,分析miR-214-3p表达与铁死亡相关蛋白的关系;应用非条件Logistic回归和限制性立方样条模型分析miR-214-3p表达与死亡的关联及剂量-反应关系;依据中位数切点对miR-214-3p表达水平与预后的相关性进行亚组分析.采用Kaplan-Meier生存曲线验证miR-214-3p表达对患者生存的影响.结果 分层回归分析结果表明,组织学级别、TNM分期、肿瘤大小、分子分型、肿瘤分化程度、远处转移对miR-214-3p表达产生显著影响(P<0.05);不同预后的乳腺癌患者亚铁离子(Fe2+)、丙二醛(MDA)、谷胱甘肽(GSH)差异及转铁蛋白、转铁蛋白受体1(TfR1)、铁转运蛋白(FPN)、铁蛋白重链1(FTH1)均具有统计学意义(P<0.05);通过Logistic回归分析可知,校正混杂因素后,转铁蛋白、TfR1、FPN、FTH1与miR-214-3p表达密切相关(P<0.05).限制性立方样条模型结果显示,miR-214-3p表达水平与死亡的关联强度呈负相关(P<0.05),存在非线性剂量-反应关系(P<0.05);亚组分析结果显示,miR-214-3p表达与预后的关系稳定存在,且亚组间不存在交互作用(P交互>0.05);miR-214-3p低表达患者与miR-214-3p高表达患者生存率均存在统计学差异(P<0.05).结论 miR-214-3p低表达与乳腺癌进展密切相关,且通过调控与铁死亡相关的蛋白通路来影响乳腺癌细胞的铁死亡.
The effect of miR-214-3p expression pattern on iron death in breast cancer and its association with clinicopathological features
Objective To investigate the effect of miR-214-3p expression pattern on iron death in breast cancer and its correlation with clinicopathological features.Methods A total of 144 breast cancer patients admitted to The Affiliated Lianyungang Oriental Hospital of Kangda College of Nanjing Medical University from February 2020 to March 2023 were selected as the study objects to analyze the relationship between miR-214-3p expression level and clinical characteristics.Hierarchical regression model was used to analyze the relationship between different clinical features and miR-214-3p expres-sion.The patients were also divided into death group(n=50)and survival group(n=94)according to the prognosis.The gen-eral data and iron-death related indicators of the two patients were compared,and the relationship between miR-214-3p ex-pression and iron-death related proteins was analyzed by Logistic regression analysis and correction model.The correlation between miR-214-3p expression and death and the dose-response relationship were analyzed by unconditioned Logistic re-gression and restricted cubic spline model.Subgroup analysis of the correlation between miR-214-3p expression level and prognosis was performed according to the median tangential point.Kaplan-Meier survival curve was used to verify the effect of miR-214-3p expression on patient survival.Results Hierarchical regression analysis showed that histological grade,TNM stage,tumor size,molecular type,tumor differentiation degree and distant metastasis had significant effects on the expression of miR-214-3p(P<0.05).There were significant differences in ferrous ion(Fe2+),malondialdehyde(MDA)and glutathione(GSH)among breast cancer patients with different prognosis(P<0.05).Logistic regression analysis showed that after adjusting for confounding factors,transferrin,transferrin receptor 1(TfR1),ferritin transporter(FPN)and ferritin heavy chain 1(FTH1)were closely related to the expression of miR-214-3p(P<0.05).The results of the restricted cubic spline model showed that the expression level of miR-214-3p was negatively correlated with the intensity of the association with death(P<0.05),and there was a nonlinear dose-response relationship(P<0.05).Subgroup analysis showed that the relationship between miR-214-3p expression and prognosis was stable,and there was no interaction between subgroups(Pinteraction>0.05).The survival rates of patients with low expression of miR-214-3p and patients with high expression of miR-214-3p were statistically different(P<0.05).Conclusion The low expression of miR-214-3p is closely related to the progression of breast cancer,and affects the iron death of breast cancer cells by regulating the protein pathway associated with iron death.

miR-214-3pbreast canceriron deathprognosis

胡双洁、章勇、薄维波、刘宜翔

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南京医科大学康达学院附属连云港东方医院检验科,江苏连云港 222042

南京医科大学康达学院附属连云港东方医院普外科,江苏连云港 222042

miR-214-3p 乳腺癌 铁死亡 预后

连云港市妇幼健康科研项目

F202313

2024

中国优生与遗传杂志
中国优生科学协会

中国优生与遗传杂志

CSTPCD
影响因子:0.527
ISSN:1006-9534
年,卷(期):2024.32(9)