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胱抑素E/M与三阴性乳腺癌临床病理特征及预后的相关性

Correlation of Cystatin E/M with Clinicopathological Features and Prognosis in Triple-Negative Breast Cancer.

作者信息

Li Quan, Zheng Zhou-Ci, Ni Chun-Jue, Jin Wen-Xu, Jin Yi-Xiang, Chen Yao, Zhang Xiao-Hua, Chen En-Dong, Cai Ye-Feng

机构信息

Department of Breast and Thyroid Surgery, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

Department of Anesthesiology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

出版信息

Ann Clin Lab Sci. 2018 Jan;48(1):40-44.

Abstract

BACKGROUND

Among all kinds of breast cancer, triple-negative breast cancer (TNBC) is the most aggressive, with the poorest prognosis and highest mortality rates. Thus, novel biomarkers that personalize the therapeutic regimen and evaluate prognosis for TNBC patients should be determined.

METHODS

We analyzed the cystatin E/M (CST6) expression profiles of 161 TNBC tissues and 14 noncancerous tissues through multiple statistical analyses. We also investigated the relationship of CST6 expression with clinical parameters and evaluated the prognostic value of CST6 in 161 TNBC patients.

RESULTS

CST6, a member of the cystatin superfamily, was remarkably more up-regulated in TNBC tissues than in adjacent normal breast tissues. High CST6 expression was frequently observed in white people and associated with a high risk of lymph-node metastasis. Cox regression analysis confirmed that the high CST6 expression was an independent predictor of disease-free survival in TNBC. Kaplan-Meier analysis further revealed that high CST6 expression caused a low disease-free survival rate.

CONCLUSION

CST6 is involved in the progression of TNBC and may act as a tumor-promoter gene. A systematic literature review shows that our study is the first to explore the relationship between CST6 and TNBC.

摘要

背景

在所有类型的乳腺癌中,三阴性乳腺癌(TNBC)侵袭性最强,预后最差,死亡率最高。因此,应确定能够使TNBC患者治疗方案个性化并评估预后的新型生物标志物。

方法

我们通过多种统计分析方法,分析了161例TNBC组织和14例非癌组织中胱抑素E/M(CST6)的表达谱。我们还研究了CST6表达与临床参数之间的关系,并评估了CST6在161例TNBC患者中的预后价值。

结果

CST6是胱抑素超家族的成员之一,在TNBC组织中的上调程度明显高于相邻的正常乳腺组织。在白人中经常观察到CST6高表达,且与淋巴结转移风险高相关。Cox回归分析证实,CST6高表达是TNBC无病生存期的独立预测因子。Kaplan-Meier分析进一步表明,CST6高表达导致无病生存率较低。

结论

CST6参与TNBC的进展,可能作为一种肿瘤促进基因发挥作用。一项系统的文献综述表明,我们的研究首次探讨了CST6与TNBC之间的关系。

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