LncRNA-MALAT1 promotes triple-negative breast cancer progression and function as ceRNA to target REEP5 by sponging miR-106a-5p

被引:0
作者
Yang, Qiu-hui [1 ]
Fu, Ye-qin [2 ]
Feng, Wei-liang [2 ]
Mao, Jie-fei [2 ]
Xu, Ning [2 ]
Liu, Qing [1 ]
Yan, Qian-jun [1 ]
Yang, Hong-jian [2 ]
Zhang, Xi-ping [2 ]
机构
[1] Zhejiang Chinese Med Univ, Zhejiang Prov Hosp Tradit Chinese Med, Affiliated Hosp 1, Hangzhou 310006, Zhejiang, Peoples R China
[2] Chinese Acad Sci, Zhejiang Canc Hosp, HIM, Dept Breast Surg, Hangzhou 310022, Zhejiang, Peoples R China
关键词
Triple negative breast cancer (TNBC); Long non-coding RNA (lncRNA); Metastasis-associated lung adenocarcinoma transcript 1 (MALAT1); Competing endogenous RNA (ceRNA); Biomarkers; Prognosis; AXIS; PROLIFERATION; MICRORNA; LNCRNA; ROLES;
D O I
10.1186/s40001-025-02420-x
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Axillary lymph node metastasis (ALNM) in triple negative breast cancer (TNBC) will lead to poor prognosis. Recent studies have shown that long non-coding RNAs (lncRNAs) were involved in the progression of tumors. This study aimed to explore the role and mechanism of lncRNA-MALAT1 in the progression of TNBC and its relationship with ALNM. MALAT1 is highly expressed in TNBC cells lines, tumor tissues and serum, and it is positively correlated with the degree of ALNM. In addition, MALAT1 can act as a competitive endogenous RNA (ceRNA) that regulates cellular biological behavior by competitively binding to miR-106a-5p with REEP5. In conclusion, our results show that MALAT1 could function as ceRNA promote the proliferation, invasion and metastasis of TNBC cells through MALAT1/miR-106a-5p/REEP5 axis, which is expected to provide new ideas for the diagnosis of TNBC in clinic.
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页数:18
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