Recognizing and stabilizing miR-21 by chiral ruthenium(II) complexes

被引:2
|
作者
Feng, Yin [1 ]
Shu, Jing [2 ,3 ]
Yao, Liangzhong [1 ]
Lan, Yutao [3 ,4 ]
Ye, Lianbao [2 ,3 ,5 ]
Mei, Wenjie [2 ,3 ,5 ]
Ding, Ying [1 ,3 ]
机构
[1] Guangdong Pharmaceut Univ, Affiliated Hosp 1, Guangzhou 510062, Peoples R China
[2] Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
[3] Guangdong Prov Engn Ctr Mol Probe & Biomed Imagin, Guangzhou 510006, Peoples R China
[4] Guangdong Pharmaceut Univ, Sch Nursing, Guangzhou 510006, Guangdong, Peoples R China
[5] Guangdong Pharmaceut Univ, Guangzhou Key Lab Construct & Applicat New Drug S, Guangzhou 510006, Peoples R China
基金
美国国家科学基金会;
关键词
Chiral ruthenium(II) complexes; MiR-21; RNA binding property; FRET; MICROWAVE-ASSISTED SYNTHESIS; CANCER-CELLS; INVASION; DNA; MICRORNA-21; APOPTOSIS; EXPRESSION; INHIBITOR; MIGRATION; PROLIFERATION;
D O I
10.1186/s13065-020-00672-8
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
MiR-21, a non-coding miRNA with 22 nucleotides, plays an important part in the proliferation, invasion, and metastasis of tumor cells. The present study demonstrates that isomers of chiral ruthenium(II) complexes with alkynes (?-1 and Delta-1) were synthesized by Songogashira coupling reaction by using microwave-assisted synthetic technology. The isomers can recognize and stabilize miR-21, with the ?-isomer showing a stronger binding capacity than the Delta-isomer. Further studies showed that both isomers can be uptaken by MDA-MB-231 cells and enriched in the nucleus. Treatment with the ?-/Delta-isomer downregulated the expression of miR-21. In a word, the development of chiral ruthenium(II) complexes act as potential inhibitors against tumor cells by recognizing, stabilizing, and regulating the expression of miR-21.
引用
收藏
页数:7
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