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[miR-27a-3p mRNA和[具体mRNA名称未给出]在乳腺癌中的表达及其与临床病理和生存预后的关系]

[Expressions of miR-27a-3p mRNA and mRNA in Breast Cancer and the Relationship With Clinicopathology and Survival Prognosis].

作者信息

Lu Zhizhong, Li Xiling, Li Kai, Yang Siwei, Jiang Fuguo, Li Shuai, Si Haiyan, Li Junmin, Zhao Xiaoguang

机构信息

( 454002) Department of Clinical Laboratory, Jiaozuo People's Hospital, Jiaozuo 454002, China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2025 Mar 20;56(2):521-527. doi: 10.12182/20250360606.

Abstract

OBJECTIVE

To analyze the expression levels of miR-27a-3p mRNA and Yes-associated protein 1 () mRNA in breast cancer, and to explore their relationships with clinicopathological features and the survival prognosis of patients.

METHODS

A total of 130 breast cancer patients who underwent mastectomy in our hospital between January 2019 and January 2021 were enrolled. The expression levels of miR-27a-3p and mRNA in breast tumor tissues and adjacent normal breast tissues were assessed by qRT-PCR. Furthermore, the relationships between their expression and clinicopathological features, as well as the survival prognosis of patients, were investigated.

RESULTS

Compared with adjacent normal breast tissues, the expression of miR-27a-3p mRNA in breast tumor tissues was lower ( < 0.05), while that of mRNA was higher ( < 0.05). A negative correlation was observed between the expression of miR-27a-3p mRNA and mRNA in breast tumor tissues ( = -0.456, < 0.05). The expression of miR-27a-3p mRNA was correlated with tumor diameter, histological grade, tumor staging by the TNM system, lymph node metastasis, and vascular invasion in patients with breast cancer ( < 0.05). The mRNA expression was correlated with histological grade, tumor staging by the TNM system, lymph node metastasis, and vascular invasion ( < 0.05). Kaplan-Meier survival analysis revealed that the 3-year overall survival rate of the miR-27a-3p low-expression group was 71.60% (48/67), which was lower than the 91.50% (54/59) of the miR-27a-3p high-expression group (log-rank = 8.211, = 0.004). The 3-year overall survival rate of the high-expression group was 73.80% (45/61), lower than that of the low-expression group (87.70%, 57/65) (log-rank =4.429, = 0.035). Multivariate regression analysis indicated that lymph node metastasis (hazard ratio [HR] = 1.409; 95% CI, 1.057-1.644; = 0.046), vascular invasion (HR = 1.541; 95% CI, 1.076-1.869; = 0.045), low miR-27a-3p mRNA expression (HR = 0.593; 95% CI, 0.388-0.925; = 0.018), and high mRNA expression (HR = 0.628; 95% CI, 0.405-0.912; = 0.022) were relevant factors affecting the 3-year overall survival of patients with breast cancer.

CONCLUSION

A significant downregulation of miR-27a-3p mRNA and upregulation of mRNA are observed in breast tumor tissues. The low expression of miR-27a-3p mRNA and the high expression of mRNA are associated with adverse clinicopathological features and poor survival prognosis, and are risk factors affecting the 3-year overall survival of patients with breast cancer. They show promise as new potential therapeutic targets for breast cancer.

摘要

目的

分析miR-27a-3p mRNA和Yes相关蛋白1(YAP1)mRNA在乳腺癌中的表达水平,并探讨它们与临床病理特征及患者生存预后的关系。

方法

选取2019年1月至2021年1月在我院接受乳房切除术的130例乳腺癌患者。采用qRT-PCR检测乳腺癌组织及癌旁正常乳腺组织中miR-27a-3p和YAP1 mRNA的表达水平。此外,研究它们的表达与临床病理特征以及患者生存预后的关系。

结果

与癌旁正常乳腺组织相比,乳腺癌组织中miR-27a-3p mRNA的表达较低(P<0.05),而YAP1 mRNA的表达较高(P<0.05)。乳腺癌组织中miR-27a-3p mRNA与YAP1 mRNA的表达呈负相关(r=-0.456,P<0.05)。miR-27a-3p mRNA的表达与乳腺癌患者的肿瘤直径、组织学分级、TNM系统肿瘤分期、淋巴结转移及血管侵犯相关(P<0.05)。YAP1 mRNA表达与组织学分级、TNM系统肿瘤分期、淋巴结转移及血管侵犯相关(P<0.05)。Kaplan-Meier生存分析显示,miR-27a-3p低表达组的3年总生存率为71.60%(48/67),低于miR-27a-3p高表达组的91.50%(54/59)(log-rank χ²=8.211,P=0.004)。YAP1高表达组的3年总生存率为73.80%(45/61),低于YAP1低表达组的87.70%(57/65)(log-rank χ²=4.429,P=0.035)。多因素回归分析表明,淋巴结转移(风险比[HR]=1.409;95%置信区间,1.057-1.644;P=0.046)、血管侵犯(HR=1.541;95%置信区间,1.076-1.869;P=0.045)、miR-27a-3p mRNA低表达(HR=0.593;95%置信区间,0.3 .88-0.925;P=0.018)和YAP1 mRNA高表达(HR=0.628;95%置信区间,0.405-0.912;P=0.022)是影响乳腺癌患者3年总生存的相关因素。

结论

乳腺癌组织中miR-27a-3p mRNA显著下调,YAP1 mRNA上调。miR-27a-3p mRNA低表达和YAP1 mRNA高表达与不良临床病理特征及生存预后不良相关,是影响乳腺癌患者3年总生存的危险因素。它们有望成为乳腺癌新的潜在治疗靶点。

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