RETRACTED: MicroRNA-448 suppresses osteosarcoma cell proliferation and invasion through targeting EPHA7 (Retracted Article)

被引:29
作者
Wu, Xiangkun [1 ]
Yan, Lihua [2 ]
Liu, Yongxi [1 ]
Xian, Wenfeng [1 ]
Wang, Liuyu [1 ]
Ding, Xunmeng [1 ]
机构
[1] Nanyang Second Peoples Hosp, Dept Orthopaed Surg, Nanyang, Henan, Peoples R China
[2] Nanyang Second Peoples Hosp, Dept Med Oncol, Nanyang, Henan, Peoples R China
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; BREAST-CANCER; LUNG ADENOCARCINOMA; COLORECTAL-CANCER; GASTRIC-CANCER; IN-VITRO; EXPRESSION; METASTASIS; PROMOTES; CARCINOMA;
D O I
10.1371/journal.pone.0175553
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Osteosarcoma is the most common type of malignant bone tumor, often affecting adolescents and children. MicroRNAs (miRNAs) are a group of small, non-protein coding, endogenous RNAs that play critical roles in osteosarcoma tumorigenesis. In our study, we demonstrated that miR-448 expression was downregulated in osteosarcoma tissues and cell lines. Overexpression of miR-448 suppressed osteosarcoma cell proliferation, colony formation and migration. Moreover, we found that EPHA7 was a direct target gene of miR-448 in osteosarcoma cells. We further demonstrated that the EPHA7 expression level was upregulated in osteosarcoma tissues. Interestingly, the expression level of EPHA7 was inversely correlated with the expression level of miR-448 in osteosarcoma tissues. In addition, elevated expression of miR-448 suppressed osteosarcoma cell proliferation and invasion through targeting EPHA7. Taken together, these findings suggest that miR-448 functioned as a tumor suppressor gene in the development of osteosarcoma through targeting EPHA7.
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页数:10
相关论文
共 41 条
[1]  
Ahmad A, 2014, AM J TRANSL RES, V6, P384
[2]   miR-15a and miR-16-1 downregulate CCND1 and induce apoptosis and cell cycle arrest in osteosarcoma [J].
Cai, Cheng-Kui ;
Zhao, Guang-Yi ;
Tian, Li-Ying ;
Liu, Lie ;
Yan, Kang ;
Ma, Yun-Lei ;
Ji, Zhen-Wei ;
Li, Xiao-Xiang ;
Han, Kang ;
Gao, Jie ;
Qiu, Xiu-Chun ;
Fan, Qing-Yu ;
Yang, Tong-Tao ;
Ma, Bao-An .
ONCOLOGY REPORTS, 2012, 28 (05) :1764-1770
[3]   miR-16 inhibits cell proliferation by targeting IGF1R and the Raf1-MEK1/2-ERK1/2 pathway in osteosarcoma [J].
Chen, Lei ;
Wang, Qing ;
Wang, Guo-dong ;
Wang, Hua-song ;
Huang, Yong ;
Liu, Xi-ming ;
Cai, Xian-hua .
FEBS LETTERS, 2013, 587 (09) :1366-1372
[4]   Analysis of proliferation and apoptotic induction by 20 steroid glycosides in 143B osteosarcoma cells invitro [J].
Delebinski, C. I. ;
Georgi, S. ;
Kleinsimon, S. ;
Twardziok, M. ;
Kopp, B. ;
Melzig, M. F. ;
Seifert, G. .
CELL PROLIFERATION, 2015, 48 (05) :600-610
[5]   miR-491-5p-induced apoptosis in ovarian carcinoma depends on the direct inhibition of both BCL-XL and EGFR leading to BIM activation [J].
Denoyelle, C. ;
Lambert, B. ;
Meryet-Figuiere, M. ;
Vigneron, N. ;
Brotin, E. ;
Lecerf, C. ;
Abeilard, E. ;
Giffard, F. ;
Louis, M-H ;
Gauduchon, P. ;
Juin, P. ;
Poulain, L. .
CELL DEATH & DISEASE, 2014, 5 :e1445-e1445
[6]   MicroRNA-145 targets vascular endothelial growth factor and inhibits invasion and metastasis of osteosarcoma cells [J].
Fan, Lei ;
Wu, Qiang ;
Xing, Xiaojuan ;
Wei, Yulong ;
Shao, Zengwu .
ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2012, 44 (05) :407-414
[7]   Clinical Relevance and Therapeutic Significance of MicroRNA-133a Expression Profiles and Functions in Malignant Osteosarcoma-Initiating Cells [J].
Fujiwara, Tomohiro ;
Katsuda, Takeshi ;
Hagiwara, Keitaro ;
Kosaka, Nobuyoshi ;
Yoshioka, Yusuke ;
Takahashi, Ryou-U ;
Takeshita, Fumitaka ;
Kubota, Daisuke ;
Kondo, Tadashi ;
Ichikawa, Hitoshi ;
Yoshida, Akihiko ;
Kobayashi, Eisuke ;
Kawai, Akira ;
Ozaki, Toshifumi ;
Ochiya, Takahiro .
STEM CELLS, 2014, 32 (04) :959-973
[8]   The emerging role of tumor-suppressive microRNA-218 in targeting glioblastoma sternness [J].
Gao, Xingchun ;
Jin, Weilin .
CANCER LETTERS, 2014, 353 (01) :25-31
[9]  
Gao YS, 2015, AM J TRANSL RES, V7, P2519
[10]   MiR-448 promotes glycolytic metabolism of gastric cancer by downregulating KDM2B [J].
Hong, Xuehui ;
Xu, Yang ;
Qiu, Xingfeng ;
Zhu, Yuekun ;
Feng, Xing ;
Ding, Zhijie ;
Zhang, Shifeng ;
Zhong, Lifeng ;
Zhuang, Yifan ;
Su, Chen ;
Hong, Xinya ;
Cai, Jianchun .
ONCOTARGET, 2016, 7 (16) :22092-22102