Small Players With Big Roles: MicroRNAs as Targets to Inhibit Breast Cancer Progression

被引:0
作者
Greene, Stephanie B. [2 ]
Herschkowitz, Jason I. [1 ]
Rosen, Jeffrey M. [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Program Dev Biol, Houston, TX 77030 USA
关键词
Breast cancer; miRNA; novel therapeutics; stem cells; ESTROGEN-RECEPTOR-ALPHA; EPITHELIAL-MESENCHYMAL TRANSITION; TUMOR-SUPPRESSOR GENE; MESSENGER-RNA DECAY; CELL-CYCLE ARREST; MIR-200; FAMILY; STEM-CELLS; DOWN-REGULATION; LUNG-CANCER; E-CADHERIN;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
As modulators of gene expression, microRNAs (miRNAs) are essential for normal development. Not surprisingly, aberrant expression of miRNAs is associated with many diseases, including cancer. Studies of various breast cancer subtypes have demonstrated that, like gene expression profiles and pathological differences, miRNA profiles can distinguish various tumor subtypes. Over the last few years, roles for miRNAs during many stages of breast cancer progression have been established. This includes potential breast cancer associated polymorphisms in miRNA target sites or miRNAs themselves, miRNAs that can act as tumor suppressors or oncogenes, and miRNAs that can modulate metastatic spread. Recent studies have also suggested key roles for miRNAs in regulating cancer stem cells. Thus, miRNAs have now become important therapeutic targets. This can be achieved by replacing miRNA expression where it has been lost or decreased, or conversely by inhibiting miRNA expression where it has been amplified or overexpressed in cancers. Ultimately, miRNAs should provide both important prognostic biomarkers as well as new targetable molecules for the treatment of breast cancer.
引用
收藏
页码:1059 / 1073
页数:15
相关论文
共 50 条
  • [21] Dual roles of CCN proteins in breast cancer progression
    Celina G. Kleer
    Journal of Cell Communication and Signaling, 2016, 10 : 217 - 222
  • [22] Roles and Mechanisms of Deubiquitinases (DUBs) in Breast Cancer Progression and Targeted Drug Discovery
    Li, Sixuan
    Zhang, Hongquan
    Wei, Xiaofan
    LIFE-BASEL, 2021, 11 (09):
  • [23] MicroRNAs in HPV associated cancers: small players with big consequences
    Satapathy, Sandeep
    Batra, Jyotsna
    Jeet, Varinder
    Thompson, Erik W.
    Punyadeera, C.
    EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2017, 17 (07) : 711 - 722
  • [24] MicroRNAs in colorectal cancer: Small molecules with big functions
    Xuan, Yu
    Yang, Huiliang
    Zhao, Linjie
    Lau, Wayne Bond
    Lau, Bonnie
    Ren, Ning
    Hu, Yuehong
    Yi, Tao
    Zhao, Xia
    Zhou, Shengtao
    Wei, Yuquan
    CANCER LETTERS, 2015, 360 (02) : 89 - 105
  • [25] MicroRNAs: Small molecules with big roles in neurodevelopment and diseases
    Sun, Emily
    Shi, Yanhong
    EXPERIMENTAL NEUROLOGY, 2015, 268 : 46 - 53
  • [26] The roles of microRNAs in the progression of castration-resistant prostate cancer
    Kojima, Satoko
    Goto, Yusuke
    Naya, Yukio
    JOURNAL OF HUMAN GENETICS, 2017, 62 (01) : 25 - 31
  • [27] ZEB1-repressed microRNAs inhibit autocrine signaling that promotes vascular mimicry of breast cancer cells
    Langer, E. M.
    Kendsersky, N. D.
    Daniel, C. J.
    Kuziel, G. M.
    Pelz, C.
    Murphy, K. M.
    Capecchi, M. R.
    Sears, R. C.
    ONCOGENE, 2018, 37 (08) : 1005 - 1019
  • [28] Breast cancer-associated fibroblasts: their roles in tumor initiation, progression and clinical applications
    Qiao, Aixiu
    Gu, Feng
    Guo, Xiaojing
    Zhang, Xinmin
    Fu, Li
    FRONTIERS OF MEDICINE, 2016, 10 (01) : 33 - 40
  • [29] MicroRNAs, a subpopulation of regulators, are involved in breast cancer progression through regulating breast cancer stem cells (Review)
    Fan, Xuemei
    Chen, Wei
    Fu, Ziyi
    Zeng, Lihua
    Yin, Yongmei
    Yuan, Hongyan
    ONCOLOGY LETTERS, 2017, 14 (05) : 5069 - 5076
  • [30] Exosomal microRNAs (exomiRs): Small molecules with a big role in cancer
    Bhome, Rahul
    Del Vecchio, Filippo
    Lee, Gui-Han
    Bullock, Marc D.
    Primrose, John N.
    Sayan, A. Emre
    Mirnezami, Alex H.
    CANCER LETTERS, 2018, 420 : 228 - 235