Deciphering the code: the pivotal role of lncRNAs in advancing TNBC therapy

被引:2
作者
Chen, Weiping [1 ]
Pan, Zhiyong [2 ]
Feng, Zhengfu [2 ]
Wang, Xin [2 ]
Zhu, Song [2 ]
机构
[1] Guangzhou Med Univ, Qingyuan Peoples Hosp, Affiliated Qingyuan Hosp, Dept Resp, Qingyuan, Peoples R China
[2] Guangzhou Med Univ, Qingyuan Peoples Hosp, Affiliated Qingyuan Hosp, Dept Radiotherapy, Qingyuan, Peoples R China
基金
中国国家自然科学基金;
关键词
triple-negative breast cancer (TNBC); long non-coding RNAs (lncRNAs); therapeutic targets; gene expression regulation; precision medicine; NEGATIVE BREAST-CANCER; NONCODING RNA GAS5; CELLS; PROMOTES; PROLIFERATION; INVASION; LOCALIZATION; PROGRESSION; EXPRESSION;
D O I
10.3389/fonc.2024.1450980
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple-negative breast cancer (TNBC) represents the most formidable subtype of breast cancer, characterized by a notable dearth in targeted therapeutic options. Deciphering the underlying molecular mechanisms of TNBC is pivotal for improving patient outcomes. Recent scientific advancements have spotlighted long non-coding RNAs (lncRNAs) as key players in the genesis, progression, and metastasis of cancers. This review delineates the significant influence of lncRNAs on the advancement, detection, and neoadjuvant chemotherapy efficacy in TNBC, detailing the diverse expression patterns of aberrant lncRNAs. The paper explores the specific mechanisms by which lncRNAs regulate gene expression in both the nucleus and cytoplasm, with a special focus on their involvement in TNBC's post-transcriptional landscape. Thorough investigations into TNBC-associated lncRNAs not only forge new avenues for early diagnosis and potent treatment strategies but also highlight these molecules as promising therapeutic targets, heralding an era of personalized and precision medicine in TNBC management.
引用
收藏
页数:10
相关论文
共 82 条
[61]   LncRNA DANCR contributes to tumor progression via targetting miR-216a-5p in breast cancer: lncRNA DANCR contributes to tumor progression [J].
Tao, Weiyang ;
Wang, Chunyang ;
Zhu, Bifa ;
Zhang, Guoqiang ;
Pang, Da .
BIOSCIENCE REPORTS, 2019, 39
[62]   LINC00096 Promotes the Proliferation and Invasion by Sponging miR-383-5p and Regulating RBM3 Expression in Triple-Negative Breast Cancer [J].
Tian, Yanyan ;
Xia, Shuguan ;
Ma, Mingde ;
Zuo, Yonggang .
ONCOTARGETS AND THERAPY, 2019, 12 :10569-10578
[63]   Clinical Importance of the lncRNA NEAT1 in Cancer Patients Treated with Immune Checkpoint Inhibitors [J].
Toker, Joseph ;
Iorgulescu, J. Bryan ;
Ling, Alexander L. ;
Villa, Genaro R. ;
Gadet, Josephina A. M. A. ;
Parida, Laxmi ;
Getz, Gad ;
Wu, Catherine J. ;
Reardon, David A. ;
Chiocca, E. Antonio ;
Mineo, Marco .
CLINICAL CANCER RESEARCH, 2023, 29 (12) :2226-2238
[64]   Systemic Delivery of Tumor-Targeting siRNA Nanoparticles against an Oncogenic LncRNA Facilitates Effective Triple-Negative Breast Cancer Therapy [J].
Vaidya, Amita M. ;
Sun, Zhanhu ;
Ayat, Nadia ;
Schilb, Andrew ;
Liu, Xujie ;
Jiang, Hongfa ;
Sun, Da ;
Scheidt, Josef ;
Qian, Victoria ;
He, Siyuan ;
Gilmore, Hannah ;
Schiemann, William P. ;
Lu, Zheng-Rong .
BIOCONJUGATE CHEMISTRY, 2019, 30 (03) :907-919
[65]   ALDH1A3-regulated long non-coding RNA NRAD1 is a potential novel target for triple-negative breast tumors and cancer stem cells [J].
Vidovic, Dejan ;
Huynh, Thomas T. ;
Konda, Prathyusha ;
Dean, Cheryl ;
Cruickshank, Brianne M. ;
Sultan, Mohammad ;
Coyle, Krysta M. ;
Gujar, Shashi ;
Marcato, Paola .
CELL DEATH AND DIFFERENTIATION, 2020, 27 (01) :363-378
[66]   LINC01096 knockdown inhibits progression of triple-negative breast cancer by increasing miR-3130-3p [J].
Wang, G-P ;
Mou, Z-L ;
Xu, Y-Y ;
Liu, G-X ;
Wang, D-M ;
Zhang, H-P .
EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES, 2019, 23 (17) :7445-7456
[67]   Long non-coding RNA FTH1P3 activates paclitaxel resistance in breast cancer through miR-206/ABCB1 [J].
Wang, Ruoming ;
Zhang, Tengteng ;
Yang, Zhen ;
Jiang, Chunxia ;
Seng, Jingjing .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2018, 22 (09) :4068-4075
[68]   Endogenous miRNA Sponge lincRNA-RoR Regulates Oct4, Nanog, and Sox2 in Human Embryonic Stem Cell Self-Renewal [J].
Wang, Yue ;
Xu, Zhenyu ;
Jiang, Junfeng ;
Xu, Chen ;
Kang, Jiuhong ;
Xiao, Lei ;
Wu, Minjuan ;
Xiong, Jun ;
Guo, Xiaocan ;
Liu, Houqi .
DEVELOPMENTAL CELL, 2013, 25 (01) :69-80
[69]   Structure of LINC00511-siRNA-conjugated nanobubbles and improvement of cisplatin sensitivity on triple negative breast cancer [J].
Wu, Bolin ;
Yuan, Yanchi ;
Han, Xue ;
Wang, Qiucheng ;
Shang, Haitao ;
Liang, Xitian ;
Jing, Hui ;
Cheng, Wen .
FASEB JOURNAL, 2020, 34 (07) :9713-9726
[70]  
Wu FL, 2018, INT J CLIN EXP PATHO, V11, P3943