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

被引:16
作者
Ryoo, Soo-Ryoon [1 ,2 ]
Yim, Yeajee [1 ,2 ]
Kim, Young-Kwan [3 ]
Park, Il-Soo [1 ]
Na, Hee-Kyung [4 ]
Lee, Jieon [5 ]
Jang, Hongje [6 ]
Won, Cheolhee [7 ]
Hong, Sungwoo [8 ,9 ]
Kim, Sung-Yon [1 ]
Jeon, Noo Li [10 ]
Song, Joon Myong [11 ]
Min, Dal-Hee [1 ,2 ,7 ]
机构
[1] Seoul Natl Univ, Dept Chem, Seoul 08826, South Korea
[2] Seoul Natl Univ, IBS, Ctr RNA Res, Seoul 08826, South Korea
[3] KIST, Carbon Composite Mat Res Ctr, Jeonbuk 55324, South Korea
[4] KRISS, Ctr Nanobio Measurement, Daejeon 34113, South Korea
[5] KIT, Predict Toxicol Dept, Daejeon 34114, South Korea
[6] Kwangwoon Univ, Dept Chem, 20 Gwangwoon Ro, Seoul 01897, South Korea
[7] Lemonex Inc, Inst Biotherapeut Convergence Technol, Seoul 08826, South Korea
[8] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 34141, South Korea
[9] Inst for Basic Sci Korea, Ctr Catalyt Hydrocarbon Functionalizat, Daejeon 34141, South Korea
[10] Seoul Natl Univ, Dept Mech & Aerosp Engn, Seoul 08826, South Korea
[11] Seoul Natl Univ, Coll Pharm, Seoul 08826, South Korea
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
基金
新加坡国家研究基金会;
关键词
CANCER; MIR-21; OVEREXPRESSION; PROLIFERATION; PROFILES; TARGETS; ACID; RNA;
D O I
10.1038/s41598-018-29633-x
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
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
页数:10
相关论文
共 41 条
  • [1] MicroRNAs: Target Recognition and Regulatory Functions
    Bartel, David P.
    [J]. CELL, 2009, 136 (02) : 215 - 233
  • [2] Buscaglia Lindsey E Becker, 2011, Chin J Cancer, V30, P371
  • [3] Overexpression of miR-21 Promotes an In vitro Metastatic Phenotype by Targeting the Tumor Suppressor RHOB
    Connolly, Erin C.
    Van Doorslaer, Koenraad
    Rogler, Leslie E.
    Rogler, Charles E.
    [J]. MOLECULAR CANCER RESEARCH, 2010, 8 (05) : 691 - 700
  • [4] Programmed cell death 4 (PDCD4) is an important functional target of the microRNA miR-21 in breast cancer cells
    Frankel, Lisa B.
    Christoffersen, Nanna R.
    Jacobsen, Anders
    Lindow, Morten
    Krogh, Anders
    Lund, Anders H.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (02) : 1026 - 1033
  • [5] MicroRNA gene expression during retinoic acid-induced differentiation of human acute promyelocytic leukemia
    Garzon, R.
    Pichiorri, F.
    Palumbo, T.
    Visentini, M.
    Aqeilan, R.
    Cimmino, A.
    Wang, H.
    Sun, H.
    Volinia, S.
    Alder, H.
    Calin, G. A.
    Liu, C-G
    Andreeff, M.
    Croce, C. M.
    [J]. ONCOGENE, 2007, 26 (28) : 4148 - 4157
  • [6] MicroRNAs as newer therapeutic targets: A big hope from a tiny player
    Ghelani, Hardik S.
    Rachchh, Manish A.
    Gokani, Rina H.
    [J]. JOURNAL OF PHARMACOLOGY & PHARMACOTHERAPEUTICS, 2012, 3 (03) : 217 - 227
  • [7] The noncoding RNA, miR-126, suppresses the growth of neoplastic cells by targeting phosphatidylinositol 3-kinase signaling and is frequently lost in colon cancers
    Guo, Chunguang
    Sah, Jerome F.
    Beard, Lydia
    Willson, James K. V.
    Markowitz, Sanford D.
    Guda, Kishore
    [J]. GENES CHROMOSOMES & CANCER, 2008, 47 (11) : 939 - 946
  • [8] Exploiting the PI3K/AKT pathway for cancer drug discovery
    Hennessy, BT
    Smith, DL
    Ram, PT
    Lu, YL
    Mills, GB
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2005, 4 (12) : 988 - 1004
  • [9] Suppression of tumor proliferation and angiogenesis of hepatocellular carcinoma by HS-104, a novel phosphoinositide 3-kinase inhibitor
    Jung, Kyung Hee
    Zheng, Hong-Mei
    Jeong, Yujeong
    Choi, Myung-Joo
    Lee, Hyunseung
    Hong, Sang-Won
    Lee, Hee-Seung
    Son, Mi Kwon
    Lee, Soyoung
    Hong, Sungwoo
    Hong, Soon-Sun
    [J]. CANCER LETTERS, 2013, 328 (01) : 176 - 187
  • [10] Robust MicroRNA Stability in Degraded RNA Preparations from Human Tissue and Cell Samples
    Jung, Monika
    Schaefer, Annika
    Steiner, Isabel
    Kempkensteffen, Carsten
    Stephan, Carsten
    Erbersdobler, Andreas
    Jung, Klaus
    [J]. CLINICAL CHEMISTRY, 2010, 56 (06) : 998 - 1006