Roles of miR-17-92 Cluster in Cardiovascular Development and Common Diseases

被引:34
|
作者
Gu, Huanyu [1 ]
Liu, Zhuyuan [1 ]
Zhou, Lei [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Cardiol, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
KEY ONCOGENIC COMPONENT; PROLIFERATION; DIFFERENTIATION; EXPRESSION; MICRORNAS; FAMILY; OVEREXPRESSION; DYSREGULATION; INHIBITION; MORTALITY;
D O I
10.1155/2017/9102909
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
MicroRNAs (miRNAs and miRs) are a large class of noncoding, single-stranded, small RNA molecules. The precise control of their expression is essential for keeping tissue homeostasis and normal development of organisms. Thus, unbalanced expression of miRNAs is a hallmark of many diseases. Two to dozens of miRNAs can forminto a miRNA cluster, and the miR-17-92 cluster is one of them. Although firstly described as an oncogenic miRNA cluster, the miR-17-92 cluster has also been found to play critical role in normal cardiac development and cardiovascular disease. This review focuses on the characteristics and functions of miR-17-92 cluster in heart.
引用
收藏
页数:6
相关论文
共 50 条
  • [31] Upregulation of miR-17-92 cluster is associated with progression and lymph node metastasis in oesophageal adenocarcinoma
    Plum, Patrick Sven
    Warnecke-Eberz, Ute
    Drebber, Uta
    Chon, Seung-Hun
    Alakus, Hakan
    Hoelscher, Arnulf Heinrich
    Quaas, Alexander
    Bruns, Christiane Josephine
    Gockel, Ines
    Lorenz, Dietmar
    Metzger, Ralf
    Bollschweiler, Elfriede
    SCIENTIFIC REPORTS, 2019, 9 (1)
  • [32] Histone deacetylase inhibition in colorectal cancer cells reveals competing roles for members of the oncogenic miR-17-92 cluster
    Humphreys, Karen J.
    Cobiac, Lynne
    Le Leu, Richard K.
    Van der Hoek, Mark B.
    Michael, Michael Z.
    MOLECULAR CARCINOGENESIS, 2013, 52 (06) : 459 - 474
  • [33] SRSF3 shapes the structure of miR-17-92 cluster RNA and promotes selective processing of miR-17 and miR-20a
    Ratnadiwakara, Madara
    Bahrudeen, Mohamed N. M.
    Aikio, Erika
    Takabe, Piia
    Engel, Rebekah M.
    Zahir, Zileena
    Jarde, Thierry
    McMurrick, Paul J.
    Abud, Helen E.
    Anko, Minna-Liisa
    EMBO REPORTS, 2023, 24 (07)
  • [34] Functional polymorphisms in the promoter region of miR-17-92 cluster are associated with a decreased risk of colorectal cancer
    Sun, Ruifen
    Liang, Yundan
    Yuan, Fang
    Nie, Xinwen
    Sun, Hong
    Wang, Yanyun
    Yu, Tao
    Gao, Linbo
    Zhang, Lin
    ONCOTARGET, 2017, 8 (47) : 82531 - 82540
  • [35] The miR-17-92 cluster counteracts quiescence and chemoresistance in a distinct subpopulation of pancreatic cancer stem cells
    Cioffi, Michele
    Trabulo, Sara M.
    Sanchez-Ripoll, Yolanda
    Miranda-Lorenzo, Irene
    Lonardo, Enza
    Dorado, Jorge
    Reis Vieira, Catarina
    Carlos Ramirez, Juan
    Hidalgo, Manuel
    Aicher, Alexandra
    Hahn, Stephan
    Sainz, Bruno, Jr.
    Heeschen, Christopher
    GUT, 2015, 64 (12) : 1936 - 1948
  • [36] miR-17-92 cluster components analysis in Burkitt lymphoma: overexpression of miR-17 is associated with poor prognosis
    Robaina, Marcela Cristina
    Faccion, Roberta Soares
    Mazzoccoli, Luciano
    Rezende, Lidia Maria M.
    Queiroga, Eduardo
    Bacchi, Carlos E.
    Thomas-Tikhonenko, Andrei
    Klumb, Claudete Esteves
    ANNALS OF HEMATOLOGY, 2016, 95 (06) : 881 - 891
  • [37] The miR-17-92 cluster as a potential biomarker for the early diagnosis of gastric cancer: evidence and literature review
    Li, Hong
    Wu, Qiong
    Li, Ting
    Liu, Changhao
    Xue, Lin
    Ding, Jie
    Shi, Yongquan
    Fan, Daiming
    ONCOTARGET, 2017, 8 (28) : 45060 - 45071
  • [38] MiRNA-17 encoded by the miR-17-92 cluster increases the potential for steatosis in hepatoma cells by targeting CYP7A1
    Gong, Ruijie
    Lv, Xiaofei
    Liu, Fengqiong
    CELLULAR & MOLECULAR BIOLOGY LETTERS, 2018, 23
  • [39] The role of the miR-17-92 cluster in neurogenesis and angiogenesis in the central nervous system of adults
    Yang, Ping
    Cai, Linghu
    Zhang, Guan
    Bian, Zhiqun
    Han, Gaofeng
    JOURNAL OF NEUROSCIENCE RESEARCH, 2017, 95 (08) : 1574 - 1581
  • [40] WEE1 is a validated target of the microRNA miR-17-92 cluster in leukemia
    Brockway, Sonia
    Zeleznik-Le, Nancy J.
    CANCER GENETICS, 2015, 208 (05) : 279 - 287