High-throughput chemical screening to discover new modulators of microRNA expression in living cells by using graphene-based biosensor

被引:0
作者
Soo-Ryoon Ryoo
Yeajee Yim
Young-Kwan Kim
Il-Soo Park
Hee-Kyung Na
Jieon Lee
Hongje Jang
Cheolhee Won
Sungwoo Hong
Sung-Yon Kim
Noo Li Jeon
Joon Myong Song
Dal-Hee Min
机构
[1] Seoul National University,Department of Chemistry
[2] Seoul National University,Center for RNA Research, Institute for Basic Sciences (IBS)
[3] Korea Institute of Science and Technology (KIST),Carbon Composite Materials Research Center
[4] Center for Nano-Bio Measurement,Predictive Toxicology Department
[5] Korea Research Institute of Standards and Science (KRISS),Department of Chemistry
[6] Korea Institute of Toxicology (KIT),Department of Chemistry
[7] Kwangwoon University,Center for Catalytic Hydrocarbon Functionalizations
[8] Institute of Biotherapeutics Convergence Technology,Department of Mechanical and Aerospace Engineering
[9] Lemonex Inc,College of Pharmacy
[10] Korea Advanced Institute of Science and Technology (KAIST),undefined
[11] Institute for Basic Science (IBS),undefined
[12] Seoul National University,undefined
[13] Seoul National University,undefined
来源
Scientific Reports | / 8卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
MicroRNAs (miRNAs) are important regulatory RNAs that control gene expression in various biological processes. Therefore, control over the disease-related miRNA expression is important both for basic research and for a new class of therapeutic modality to treat serious diseases such as cancer. Here, we present a high-throughput screening strategy to identify small molecules that modulate miRNA expression in living cells. The screen enables simultaneous monitoring of the phenotypic cellular changes associated with the miRNA expression by measuring quantitative fluorescent signals corresponding to target miRNA level in living cells based on a novel biosensor composed of peptide nucleic acid and nano-sized graphene oxide. In this study, the biosensor based cellular screening of 967 compounds (including FDA-approved drugs, enzyme inhibitors, agonists, and antagonists) in cells identified four different classes of small molecules consisting of (i) 70 compounds that suppress both miRNA-21 (miR-21) expression and cell proliferation, (ii) 65 compounds that enhance miR-21 expression and reduce cell proliferation, (iii) 2 compounds that suppress miR-21 expression and increase cell proliferation, and (iv) 21 compounds that enhance both miR-21 expression and cell proliferation. We further investigated the hit compounds to correlate cell morphology changes and cell migration ability with decreased expression of miR-21.
引用
收藏
相关论文
共 63 条
  • [1] Bartel DP(2009)MicroRNAs: target recognition and regulatory functions Cell 136 215-233
  • [2] Obernosterer G(2006)Post-transcriptional regulation of microRNA expression RNA 12 1161-1167
  • [3] Leuschner PJ(2006)MiRNAs regulate miRNAs: coordinated transcriptional and post-transcriptional regulation Cell Cycle 5 2473-2476
  • [4] Alenius M(2009)Epigenetic Control of MicroRNA Expression and Aging Curr. Genomics 10 184-193
  • [5] Martinez J(2014)Therapeutic targeting of microRNAs: current status and future challenges Nature Reviews Drug Discovery 13 622-227
  • [6] Tuccoli A(2017)MicroRNA therapeutics: towards a new era for the management of cancer and other diseases Nature Reviews Drug Discovery 16 203-5891
  • [7] Poliseno L(2012)MicroRNAs as newer therapeutic targets: A big hope from a tiny player J. Pharmacol. Pharmacother. 3 217-17669
  • [8] Rainaldi G(2013)Quantitative and multiplexed microRNA sensing in living cells based on peptide nucleic acid and nano graphene oxide (PANGO) ACS Nano 7 5882-1143
  • [9] Liang R(2010)Graphene oxide nanocolloids J. Am. Chem. Soc. 132 17667-359
  • [10] Bates DJ(2013)Targeting miR-21 induces autophagy and chemosensitivity of leukemia cells Curr. Drug Targets 14 1135-1296