医学分子生物学杂志 ›› 2022, Vol. 19 ›› Issue (4): 307-313.doi: 10.3870/j.issn.1672-8009.2022.04.007

• 论著 • 上一篇    下一篇

miR-342-3p 在乳腺癌中的表达及其与临床病理特征、 远期预后的相关性

  

  1. 福建医科大学附属南平第一医院甲状腺乳腺外科 福建省南平市, 353000
  • 出版日期:2022-07-31 发布日期:2022-08-15

Expression of mir-342-3p in Breast Cancer Tissues and Its Correlation with Clinicopathological Features and Long-Term Prognosis in Patients 

  1. Department of Thyroid and Breast Surgery, Nanping First Hospital of Affiliated to Fujian Medical University, Nanping, Fujian, 353000, China
  • Online:2022-07-31 Published:2022-08-15

摘要: 目的 研究 miR-342-3p 在乳腺癌中表达及其与临床病理特征、 远期预后的相关性。 方法 选择 2014 年 1 月 ~ 2015 年 2 月期间在南平市第一医院接受乳腺癌根治术的患者作为乳腺癌组, 同期接受手术切 除的乳腺良性肿瘤患者作为对照组, 检测乳腺癌组织及乳腺良性肿瘤组织中 miR-342-3p 的表达水平, 随访 乳腺癌患者的总生存 (OS) 及无病生存 (DFS), 采用 Kaplan-Meier 曲线分析 miR-342-3p 的表达水平与 OS、 DFS 的关系, 采用 COX 比例风险模型分析 OS、 DFS 的影响因素。 在乳腺癌 MCF7 细胞中转染 miR-NC 序列及 miR-342-3p 模拟物, 检测细胞活力水平及 AKT2、 Bcl2L1、 FOXQ1 的表达水平。 结果 乳腺癌组织 中 miR-342-3p 的表达水平明显低于乳腺良性肿瘤组织 (P< 0. 05), 且不同 T 分期、 淋巴结转移、 分子分 型、 Ki-67 表达的乳腺癌组织间比较, miR-342-3p 表达水平有显著差异 (P< 0. 05)。 Kaplan-Meier 曲线分析 显示, 相比于 miR-342-3p 高表达患者, miR-342-3p 低表达患者的 DFS 和 OS 均缩短。 COX 比例风险模型分 析显示, 淋巴结转移、 Ki-67 表达、 miR-342-3p 表达是乳腺癌患者 DFS 和 OS 的影响因素。 miR-342-3p 高表 达的乳腺癌组织中 AKT2、 Bcl2L1、 FOXQ1 的表达水平低于 miR-342-3p 低表达的乳腺癌组织。 miR-342-3p 组 MCF7 细胞中细胞活力及 AKT2、 Bcl2L1、 FOXQ1 的表达水平均低于 miR-NC 组。 结论 乳腺癌中 miR-342-5p 低表达且其低表达与病理特征恶化有关, miR-342-5p 低表达是乳腺癌患者预后的影响因素, AKT2、 Bcl2L1、 FOXQ1 可能是 miR-342-5p 参与乳腺癌发展的潜在分子机制。

关键词: 乳腺癌, miR-342-5p, 病理特征, 总生存, 无病生存

Abstract: Objective To investigate the correlation of the expression of miR-342-3p with the clinicopathological features and long-term prognosis in breast cancer. Methods The breast cancer patients who received the radical mastectomy from January 2014 to February 2015 in Nanping First Hospital were included in the breast cancer group, and the patients with benign breast tumors who received the surgical resection were included in the control group. The expression level of miR-342- 3p in breast cancer tissues and benign breast tumor tissues were detected. The breast cancer patients were followed up until August 2019 to analyze their overall survival (OS) and disease-free survival (DFS). The Kaplan-Meier curve was used to analyze the relationship between the expression level of miR-342-3p and the OS and DFS of the patients. Cox proportional risk model was used to analyze the risk factors affecting the OS and DFS of the patients. The cell viability of MCF7 cells transfected with miR-NC or miR-342-3p mimics were measured. The expression levels of AKT2, Bcl2L1 and FOXQ1 were detected. Results The expression level of miR-342-3p in breast cancer tissues was significantly lower than that in benign breast tumor tissues (P < 0. 05), and statistical difference were found in patients with different T stage, status of lymph node metastasis, molecular typing and Ki-67 expression level (P< 0. 05). The Kaplan-Meier curve analysis showed that the DFS and OS were shorter in patients with lower expression level of miR-342-3p than those in patients with higher expression level of miR-342-3p. COX analysis showed that the status of lymph node metastasis and the expression levels of Ki-67 and mir-342-3p were the risk factors for DFS and OS in breast cancer patients. The expression levels of AKT2, Bcl2L1 and FOXQ1 were lower in breast cancer tissues with highly expressed miR-342-3p than those with lowly expressed miR-342-3p. The cell viability of MCF7 cells overexpressed with miR-342-3p was higher than that in control group. The expression levels of AKT2, Bcl2L1 and FOXQ1 in MCF7 cells overexpressed with miR-342-3p were lower than those in control group. Conclusion miR-342-5p is lowly expressed in breast cancer patients and correlates with the deterioration of their pathological features. Low expression of miR-342-5p is the risk factor for prognosis in breast cancer patients. AKT2, Bcl2L1 and FOXQ1 may be involved in the molecular mechanism of miR-342-5p associated breast cancer progression. 

Key words: breast cancer, miR-342-5p, pathological features, overall survival, disease free survival

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