A serum LncRNA signature for predicting prognosis of triple-negative breast cancer

被引:1
|
作者
Zhu, Ting [1 ]
Wang, Junjun [2 ]
Li, Juan [1 ]
Zhang, Qichao [1 ]
Shang, Yanyan [1 ]
Zhou, Junhao [5 ]
Min, Ling [1 ]
Lv, Bo [3 ,4 ]
Luo, Kai [1 ,6 ]
机构
[1] Guangzhou Med Univ, Dept Lab Med, Affiliated Canc Hosp & Inst, Guangzhou 510095, Guangdong, Peoples R China
[2] Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Guangdong Cardiovasc Inst, Guangzhou 510080, Guangdong, Peoples R China
[3] Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Guangdong Cardiovasc Inst, Dept Gen Practice, Guangzhou 510080, Guangdong, Peoples R China
[4] Southern Med Univ, Sch Clin Med 2, Guangzhou 510080, Guangdong, Peoples R China
[5] Southern Med Univ, Dept Urol, Affiliated Hosp 3, Guangzhou 510630, Guangdong, Peoples R China
[6] Guangzhou Med Univ, Dept Lab Med, Affiliated Canc Hosp & Inst, 78 Hengzhigang Rd, Guangzhou 510095, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
LINC00989; Triple -negative breast cancer; Exosomes; Prognosis; EXOSOMES;
D O I
10.1016/j.cca.2023.117535
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Breast cancer is the leading causes of cancer-associated mortality among women, and triple-negative breast cancer (TNBC) is an aggressive subtype of breast cancer. Long non-coding RNAs (LncRNAs) have recently been studied to predict the prognosis of various cancers, but whether it is an effective marker in TNBC is inconclusive.Methods: We used RNA-sequencing analysis to identify differentially expressed exosomal LncRNAs, and qRT-PCR assay was performed to verify dysregulated LncRNAs in multicenter validation cohorts. A signature, which was composed of LINC00989, CEA, and CA153, was then utilized to predict the progression and recurrence of TNBC. Kaplan-Meier analysis was applied to evaluate the prognostic values of the signature.Results: On the basis of RNA-sequencing analysis, we found that serum exosomal LncRNA LINC00989 was significantly up-regulated in metastatic patients of TNBC. Then LINC00989, together with clinic marker CEA and CA125, were selected to construct a prognostic signature. In both training and validation cohort, higher levels of this signature were significantly related with shorter overall and progression-free survival time. Univariate and multivariate analysis shown that the signature was the independent prognosis factor of TNBC patients.Conclusions: Our results suggested that this prognostic signature might potentially predict prognosis and recurrence of TNBC, and was worth validation in future clinical trials.
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页数:10
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