首页|miR-544a在结直肠癌组织中的表达及其意义

miR-544a在结直肠癌组织中的表达及其意义

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目的:探讨结直肠癌患者组织中微小RNA-544a(miR-544a)的表达水平及其与患者预后的关系.方法:选取2016年1月—2019年2月住院并接受手术的150例结直肠癌患者,采用实时荧光定量PCR法检测癌组织中miR-544a的表达情况,免疫组织化学法检测癌组织中Ki67、CD4、CD8表达情况.Mann-Whitney U检验、卡方检验和Fisher精确检验分析癌组织中miR-544a表达水平与患者临床病理指标的关系.单因素和多因素Cox回归分析影响结直肠癌预后的因素.Kaplan-Meier法分析结直肠癌组织中miR-544a表达水平与患者无病生存期(DFS)、总生存期(OS)的关系.结果:结直肠癌组织中miR-544a相对表达水平为1.85±0.15,高于癌旁正常组织的1.06±0.21,差异具有统计学意义(P<0.01).miR-544a表达水平与周围神经侵犯率、T分期、N分期有关(均为P<0.01),miR-544a高表达组神经侵犯率高,T、N分期较晚.免疫组织化学检测结果显示,miR-544a高表达组Ki67评分为120.2±33.7,低表达组Ki67评分为112.4±40.8,两组差异无统计学意义(P>0.05);miR-544a高表达组患者CD4、CD8评分分别为15.5±5.3和24.8±7.6,均低于miR-544a低表达组(分别为21.3±7.2和29.6±8.9),差异均具有统计学意义(均为P<0.05).单因素、多因素Cox回归分析显示肿瘤N、M分期及miR-544a表达水平与CRC患者根治术后DFS、OS显著相关(均为P<0.01).结论:结直肠癌组织中miR-544a表达水平上调,miR-544a高表达与结直肠癌患者较晚的N、M分期以及不良预后有关,且miR-544a可能是反映免疫治疗效果的潜在标志物.
Expression and significance of miR-544a in patients with colorectal cancer
OBJECTIVE:To explore expression level and clinical prognostic value of microRNA-544a (miR-544a) in tissues of colorectal cancer patients. METHODS:From January 2016 to February 2019, 150 patients with colorectal cancer were selected. Real time fluorescence quantitative PCR was used to detect expression levels of miR-544a in tissues, and immunohistochemistry was used to detect the expression of Ki67,CD4,and CD8 in tissues. Mann Whitney U-test,chi square test,and Fisher′s exact test were used to analyze relationships between miR-544a expression level in cancer tissue and clinical pathological indicators of patients. Univariate and multivariate Cox regressions were used to analyze factors affecting the prognosis of colorectal cancer. The Kaplan-Meier method was used to analyze relationships between expression levels of miR-544a in tissues and disease-free survival (DFS) and overall survival (OS) of patients. RESULTS:The relative expression level of miR-544a in colorectal cancer tissue (1.85 ± 0.15) was significantly higher than that in the adjacent normal tissues (1.06 ± 0.21) (P<0.01). The expression level of miR-544a was related to the incidence of peripheral nerve invasion,T staging,and N staging (all P<0.01),while the high expression group of miR-544a had a higher incidence of nerve invasion and a later T and N staging. The immunohistochemical results showed that the Ki67 score of the miR-544a high expression group was 120.2 ± 33.7, while the Ki67 score of the low expression group was 112.4 ± 40.8, with no significant difference between the two groups (P>0.05). The CD4 and CD8 scores of patients in the miR-544a high expression group were 15.5±5.3 and 24.8 ±7.6, respectively, lower than those in the miR-544a low expression group (21.3 ± 7.2 and 29.6 ± 8.9, respectively), with statistically significant differences (all P<0.05). Univariate and multivariate COX regression showed significant correlations between tumor N,M staging,and miR-544a expression levels and postoperative DFS and OS in CRC patients (all P<0.01). CONCLUSION:Upregulation of miR-544a expression in colorectal cancer tissue may be associated with delayed N and M stagings in colorectal cancer patients , and miR-544a may be a potential biomarker for immunotherapy efficacy.

colorectal cancermiRNAmiR-544aprognosistumor biomarker

童晶、王丹

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扬州市江都人民医院病理科,江苏 扬州225299

商丘市第一人民医院病理科,河南商丘 476005

结直肠癌 微小RNA miR-544a 预后 肿瘤标志物

2024

癌变·畸变·突变
中国环境诱变剂学会

癌变·畸变·突变

CSTPCD
影响因子:0.35
ISSN:1004-616X
年,卷(期):2024.36(2)
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