RETRACTED: Synthetic miR-145 mimic inhibits multiple myeloma cell growth in vitro and in vivo (Retracted article. See vol. 46, 2021)

被引:18
|
作者
Zhang, Qi [1 ]
Yan, Weiqun [1 ]
Bai, Yang [2 ]
Xu, Hao [1 ]
Fu, Changhao [1 ]
Zheng, Wenwen [3 ]
Zhu, Yingqiao [2 ]
Ma, Jie [1 ]
机构
[1] Jilin Univ, Sch Pharmaceut Sci, Changchun 130021, Jilin, Peoples R China
[2] Jilin Univ, Hosp 1, Changchun 130021, Jilin, Peoples R China
[3] Jilin Univ, Hosp 1, Inst Virol & AIDS Res, Changchun 130021, Jilin, Peoples R China
关键词
microRNA-145; microRNA; multiple myeloma; tumor growth; TUMOR-SUPPRESSOR; MOLECULAR PATHOGENESIS; CLINICAL-APPLICATIONS; GENE-EXPRESSION; C-MYC; CANCER; MICRORNAS; TARGETS; DEATH; METASTASIS;
D O I
10.3892/or.2014.3591
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multiple myeloma (MM) is a disease with an adverse outcome and new therapeutic strategies are required to combat this disease. It is well known that tumor-suppressor microRNA (miRNA) acts as a new potential anticancer agent. Accumulating evidence showed that microRNA-145 (miR-145) is a candidate tumor suppressor miRNA. However, whether miR-145 is involved in the development and progression of MM reamins to be determined. In the present study, we investigated the therapeutic potential of synthetic miR-145 against human MM cells in vitro and in vivo. The results showed that miR-145 was reduced in MM tissues and cell lines. Enforced expression of miR-145 by transfection with miR-145 mimics inhibited cell proliferation, migration, and the invasion abilities of H929 cells. Furthermore, our results demonstrated that the enforced expression of miR-145 in H929 cells profoundly decreased the levels of p-AKT and p-PI3K, which may contribute to some extent to the inhibition of MM cell proliferation and survival. The enforced expression of miR-145 in a xenograft mouse model suppressed tumor growth. In conclusion, our findings suggested that miR-145 may act as a tumor suppressor and contributes to the progression of MM. Additionally, miR-145 mimics is a potential therapeutic agent for the treatment of MM.
引用
收藏
页码:448 / 456
页数:9
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