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

Abstract 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 (Λ-1 and Δ-1) were synthesized by Songogashira coupling reaction...

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Main Authors: Yin Feng, Jing Shu, Liangzhong Yao, Yutao Lan, Lianbao Ye, Wenjie Mei, Ying Ding
Format: Article
Language:English
Published: BMC 2020-04-01
Series:BMC Chemistry
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13065-020-00672-8
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spelling doaj-82faed1c6de844caa09e11eb1fb9bb012020-11-25T03:31:58ZengBMCBMC Chemistry2661-801X2020-04-011411710.1186/s13065-020-00672-8Recognizing and stabilizing miR-21 by chiral ruthenium(II) complexesYin Feng0Jing Shu1Liangzhong Yao2Yutao Lan3Lianbao Ye4Wenjie Mei5Ying Ding6The First Affiliated Hospital of Guangdong Pharmaceutical UniversitySchool of Pharmacy, Guangdong Pharmaceutical UniversityThe First Affiliated Hospital of Guangdong Pharmaceutical UniversityGuangdong Province Engineering Center for Molecular Probe & Biomedical ImagingSchool of Pharmacy, Guangdong Pharmaceutical UniversitySchool of Pharmacy, Guangdong Pharmaceutical UniversityThe First Affiliated Hospital of Guangdong Pharmaceutical UniversityAbstract 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 (Λ-1 and Δ-1) were synthesized by Songogashira coupling reaction by using microwave-assisted synthetic technology. The isomers can recognize and stabilize miR-21, with the Λ-isomer showing a stronger binding capacity than the Δ-isomer. Further studies showed that both isomers can be uptaken by MDA-MB-231 cells and enriched in the nucleus. Treatment with the Λ-/Δ-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.http://link.springer.com/article/10.1186/s13065-020-00672-8Chiral ruthenium(II) complexesMiR-21RNA binding propertyFRET
collection DOAJ
language English
format Article
sources DOAJ
author Yin Feng
Jing Shu
Liangzhong Yao
Yutao Lan
Lianbao Ye
Wenjie Mei
Ying Ding
spellingShingle Yin Feng
Jing Shu
Liangzhong Yao
Yutao Lan
Lianbao Ye
Wenjie Mei
Ying Ding
Recognizing and stabilizing miR-21 by chiral ruthenium(II) complexes
BMC Chemistry
Chiral ruthenium(II) complexes
MiR-21
RNA binding property
FRET
author_facet Yin Feng
Jing Shu
Liangzhong Yao
Yutao Lan
Lianbao Ye
Wenjie Mei
Ying Ding
author_sort Yin Feng
title Recognizing and stabilizing miR-21 by chiral ruthenium(II) complexes
title_short Recognizing and stabilizing miR-21 by chiral ruthenium(II) complexes
title_full Recognizing and stabilizing miR-21 by chiral ruthenium(II) complexes
title_fullStr Recognizing and stabilizing miR-21 by chiral ruthenium(II) complexes
title_full_unstemmed Recognizing and stabilizing miR-21 by chiral ruthenium(II) complexes
title_sort recognizing and stabilizing mir-21 by chiral ruthenium(ii) complexes
publisher BMC
series BMC Chemistry
issn 2661-801X
publishDate 2020-04-01
description Abstract 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 (Λ-1 and Δ-1) were synthesized by Songogashira coupling reaction by using microwave-assisted synthetic technology. The isomers can recognize and stabilize miR-21, with the Λ-isomer showing a stronger binding capacity than the Δ-isomer. Further studies showed that both isomers can be uptaken by MDA-MB-231 cells and enriched in the nucleus. Treatment with the Λ-/Δ-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.
topic Chiral ruthenium(II) complexes
MiR-21
RNA binding property
FRET
url http://link.springer.com/article/10.1186/s13065-020-00672-8
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