[1]马彦娥,苏虎艳,王倩如,等.非小细胞肺癌组织中miR-30a和CD73的表达水平与预后相关性分析[J].现代检验医学杂志,2022,37(03):73-78.[doi:10.3969/j.issn.1671-7414.2021.03.015]
 MA Yan-e,SU Hu-yan,WANG Qian-ru,et al.Correlation Analysis of Tissue miR-30a and CD73 Expression Levels and Prognosis in Non-small Cell Lung Cancer[J].Journal of Modern Laboratory Medicine,2022,37(03):73-78.[doi:10.3969/j.issn.1671-7414.2021.03.015]
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非小细胞肺癌组织中miR-30a和CD73的表达水平与预后相关性分析()
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《现代检验医学杂志》[ISSN:/CN:]

卷:
第37卷
期数:
2022年03期
页码:
73-78
栏目:
论 著
出版日期:
2022-05-15

文章信息/Info

Title:
Correlation Analysis of Tissue miR-30a and CD73 Expression Levels and Prognosis in Non-small Cell Lung Cancer
文章编号:
1671-7414(2022)03-073-06
作者:
马彦娥苏虎艳王倩如郝光军
(榆林市第一医院肿瘤诊疗中心,陕西榆林 719000)
Author(s):
MA Yan-e SU Hu-yan WANG Qian-ru HAO Guang-jun
( Center of Cancer Diagnosis and Treatment, the First Hospital of Yulin City, Shaanxi Yulin 719000,China)
关键词:
非小细胞肺癌微小核糖核酸-30a胞外5’- 核苷酸酶生存分析
分类号:
R734.2;R730.43
DOI:
10.3969/j.issn.1671-7414.2021.03.015
文献标志码:
A
摘要:
目的 探究微小核糖核酸( micro RNA, miR)-30a,胞外 -5’核苷酸酶( ecto-5’-nucleotidase, CD73)在非小细胞肺癌( non-small cell lung cancer,NSCLC)组织中的表达及其预后相关性。方法 选取 2015年 8月~ 2019年 12月于榆林市第一医院术后病理检查证实为 NSCLC患者癌组织 120例为研究组, 50例正常癌旁组织(距离癌组织 5cm以上)为对照组,采用实时荧光定量 PCR(qRT-PCR)技术检测组织标本中 miR-30a相对表达量,免疫组织化学法检测 CD73的表达情况,分析 miR-30a,CD73表达水平与 NSCLC患者临床病理参数及生存时间之间的关系,多因素 COX回归分析影响 NSCLC患者预后的危险因素。结果 miR-30a在 NSCLC癌组织中的表达水平( 1.17±0.21)明显低于正常癌旁组织( 1.62±0.48),差异有统计学意义( t=8.521,P=0.000);CD73在 NSCLC癌组织及癌旁正常组织中的阳性表达率分别为 63.33%(76/120)和 32.00%(16/50),差异有统计学意义( χ2=13.955,P=0.000);miR-30a高表达组 NSCLC患者一年累积生存率( 86.89%)明显高于低表达组( 59.32%)(Log Rank χ2=11.652,P=0.000);CD73高表达组 NSCLC患者一年累积生存率( 58.82%)明显低于低表达组( 92.31%)(Log Rank χ2=16.894,P=0.000);多因素 COX回归分析,结果显示分化程度低( HR=1.677,95%CI:1.092~ 2.576),发生淋巴结转移(HR=1.574,95%CI: 1.043~ 2.376),miR-30a低表达( HR=1.479,95%CI:1.027~ 2.130),CD73高表达( HR=1.501,95%CI:1.059~ 2.128)是影响 NSCLC患者预后不良的危险因素。结论 NSCLC癌组织中, miR-30a表达下调, CD73表达上调,二者水平异常表达可能与 NSCLC的发生发展有关,低 miR-30a和高 CD73与患者预后不良有关。
Abstract:
Objective To investigate the expression of microRNA (miR)-30a and ecto-5’-nucleotidase (CD73) in non-small cell lung cancer (NSCLC) tissues and their prognostic correlation. Methods From August 2015 to December 2019, 120 cases of cancerous tissues from NSCLC patients confirmed by postoperative pathological examination in the First Hospital of Yulin City were selected as the study group, and 50 cases of normal adjacent tissues (more than 5cm away from cancer tissue) were selected as the control group.The relative expression of miR-30a in tissue samples was detected with quantitative real-time PCR (qRTPCR) technology,the expression of CD73 was detected with immunohistochemical method,the relationship between the expression levels of miR-30a and CD73 and the clinicopathological parameters and survival time of NSCLC patients was analyzed, the risk factors affecting the prognosis of NSCLC patients were analyzed with multivariate COX regression. Results  The expression level of miR-30a in NSCLC cancer tissues (1.17±0.21) was significantly lower than that of normal adjacent tissues (1.62±0.48), and the difference was statistically significant (t=8.521, P=0.000). The positive expression rate of CD73 in NSCLC cancer tissues and normal adjacent tissues was 63.33% (76/120) and 32.00% (16/50), respectively, and the difference was statistically significant (χ2=13.955, P=0.000).The one-year cumulative survival rate of NSCLC patients in the miR-30a high expression group (86.89%) was significantly higher than that in the low expression group (59.32%)(Log Rankχ2=11.652, P=0.000). The one-year cumulative survival rate of NSCLC patients in the CD73 high expression group (58.82%) was significantly lower than that in the low expression group(92.31%)(Log Rankχ2=16.894, P=0.000).Multivariate COX regression analysis showed low differentiation (HR=1.677, 95%CI: 1.092~2.576), lymph node metastasis(HR=1.574,95%CI:1.043 ~ 2.376), and low miR-30a expression (HR=1.479, 95%CI:1.027 ~ 2.130) and high CD73 expression (HR=1.501, 95%CI: 1.059 ~ 2.128) were risk factors affecting the poor prognosis of NSCLC patients. Conclusion In NSCLC cancer tissues, the expression of miR-30a was down-regulated and the expression of CD73 was up-regulated. The abnormal expression of both levels would be related to the occurrence and development of NSCLC. Low miR-30a and high CD73 were related to the poor prognosis of patients.

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备注/Memo

备注/Memo:
基金项目:榆林市科技计划项目(项目编号【2019】185 号-41):miR-376a 调控TRIM22-CDC14A 参与小细胞肺癌顺铂耐药性的研究。
作者简介:马彦娥(1986-), 女, 硕士研究生,主治医师,从事肺癌靶向治疗方面的研究,E-mail:m18791296328@163.com。
通讯作者:苏虎艳(1989-),女,硕士研究生,主治医师,主要从事肺癌靶向治疗方面的研究。
更新日期/Last Update: 1900-01-01