The function of miR-218 and miR-618 in postmenopausal osteoporosis

被引:4
|
作者
Wang, W. -W. [1 ]
Yang, L. [2 ]
Wu, J. [1 ]
Gao, C. [3 ]
Zhu, Y. -X. [4 ]
Zhang, D. [1 ]
Zhang, H. -X. [1 ]
机构
[1] Nanjing Med Univ, Dept Obstet & Gynecol, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Nanjing Hosp 1, Dept Orthoped, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Obstet & Gynecol, State Key Lab Reprod Med, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Jiangsu Diabet Ctr, Key Lab Human Funct Genom Jiangsu Prov, Nanjing, Jiangsu, Peoples R China
关键词
Postmenopausal osteoporosis; miR-218; miR-618; TLR-4; Nf-kB; Osteoclast differentiation; MESSENGER-RNA; OSTEOCLAST DIFFERENTIATION; MICRORNAS; APOPTOSIS; PATHWAY; WOMEN; MICE;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: Postmenopausal osteoporosis (POMP) is a serious disorder with significant physical, psychosocial, and financial consequences, which greatly reduce the postmenopausal women's life quality. The related issues of postmenopausal osteoporosis are increasingly concerned by society. Past researches have shown that miRNAs play an important role in the occurrence and development of postmenopausal osteoporosis. However, the role of miR-218 and miR-618 in the osteoporosis regulation is still unclear. MATERIALS AND METHODS: First of all, we investigated the alteration of miR-218 and miR-618 during osteoclastogenesis of RAW264.7 cells. Next, we transfected RAW264.7 cells with miR-218 or miR-618 mimics and inhibitors to explore the influences of miR-218 and miR-618 on osteoclast differentiation. Then, we conducted bioinformatics analysis and luciferase reporter assay to identify and test the target gene of miR-218 and miR-618. RESULTS: MiR-218 and miR-618 were down-regulated when RAW264.7 cells differentiated into osteoclasts. In addition, overexpression of miR-218 or miR-618 attenuated RAW264.7 cells differentiated into osteoclasts in vitro, whereas inhibition of miR-218 or miR-618 promoted this progress. This was demonstrated by increased expression of osteoclast-specific genes and TRAP staining. TLR-4 was confirmed to be the direct target of miR-218 and miR-618 by bioinformatics and luciferase reporter assay. CONCLUSIONS: These results suggested that miR-218 and miR-618 play an important role in osteoclastogenesis via TLR-4/MyD88/NF-kappa B signaling pathway. Thus, targeting miR-218 and miR-618 promise a therapeutic potential in the treatment of osteoporosis.
引用
收藏
页码:5534 / 5541
页数:8
相关论文
共 50 条
  • [41] MiR-218 suppresses cell progression by targeting APC in cervical cancer
    Mao, Yifan
    Zhang, Liya
    Li, Yuan
    Yan, Minqin
    He, Lianzhi
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2017, 10 (02): : 2259 - 2269
  • [42] MiR-618 inhibits anaplastic thyroid cancer by repressing XIAP in one ATC cell line
    Cheng, Qianpeng
    Zhang, Xingguang
    Xu, Xiuping
    Lu, Xiaofeng
    ANNALES D ENDOCRINOLOGIE, 2014, 75 (04) : 187 - 193
  • [43] CircRNA circ-ATAD1 suppresses miR-618 maturation to participate in colorectal cancer
    Cao, Li
    Dong, Guanglong
    Li, Huan
    BMC GASTROENTEROLOGY, 2022, 22 (01)
  • [44] miR-618抑制结直肠癌生长转移的机制探讨
    李敏
    张春梅
    荣耕
    王明明
    现代肿瘤医学, 2020, 28 (10) : 1698 - 1702
  • [45] Polymorphism rs2682818 in miR-618 is associated with colorectal cancer susceptibility in a Han Chinese population
    Chen, Yuetong
    Du, Mulong
    Chen, Wei
    Zhu, Lingjun
    Wu, Congye
    Zhang, Zhengdong
    Wang, Meilin
    Chu, Haiyan
    Gu, Dongying
    Chen, Jinfei
    CANCER MEDICINE, 2018, 7 (04): : 1194 - 1200
  • [46] miR-218 tissue expression level is associated with aggressive progression of gastric cancer
    Wang, X. X.
    Ge, S. J.
    Wang, X. L.
    Jiang, L. X.
    Sheng, M. F.
    Ma, J. J.
    GENETICS AND MOLECULAR RESEARCH, 2016, 15 (02):
  • [47] DECREASED MIR-218 EXPRESSION PROMOTES TUMOR CELL SURVIVAL PATHWAYS IN GLIOBLASTOMAS
    Mathew, Lijoy K.
    Skuli, Nicolas
    Mucaj, Vera
    Imtiyaz, Hongxia Z.
    Venneti, Sriram
    Lal, Priti
    Zhang, Zhongfa
    Davuluri, Ramana V.
    Koch, Cameron
    Evans, Sydney
    Simon, M. Celeste
    NEURO-ONCOLOGY, 2011, 13 : 12 - 12
  • [48] MiR-218 targets MeCP2 and inhibits heroin seeking behavior
    Yan, Biao
    Hu, Zhaoyang
    Yao, Wenqing
    Le, Qiumin
    Xu, Bo
    Liu, Xing
    Ma, Lan
    SCIENTIFIC REPORTS, 2017, 7
  • [49] Decreased expression of miR-218 is associated with poor prognosis in patients with colorectal cancer
    Yu, Hong
    Gao, Guangzhong
    Jiang, Lin
    Guo, Lingchuan
    Lin, Mei
    Jiao, Xiao
    Jia, Weiguang
    Huang, Junxing
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2013, 6 (12): : 2904 - 2911
  • [50] Sex differences and therapeutic effects of miR-218 during prefrontal cortex development
    Morgunova, Alice
    Giroux, Michel
    Hernandez, Giovanni
    Flores, Cecilia
    JOURNAL OF PSYCHIATRY & NEUROSCIENCE, 2022, 47 (03): : S18 - S18