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Multiplex bioimaging of piRNA molecular pathway-regulated theragnostic effects in a single breast cancer cell using a piRNA molecular beacon

Authors
Lee, Youn JungMoon, Sung UngPark, Min GeunJung, Woon YongPark, Yong KeunSong, Sung KyuRyu, Je GyuLee, Yong SeungHeo, Hye JungGu, Ha NaCho, Su JeongAli, Bahy A.Al-Khedhairy, Abdulaziz A.Lee, IlkyunKim, Soonhag
Issue Date
Sep-2016
Publisher
ELSEVIER SCI LTD
Keywords
Molecular beacon; piRNA-36026; Cancer theragnosis; Multiplex bioimaging; Molecular pathway
Citation
BIOMATERIALS, v.101, pp.143 - 155
Indexed
SCIE
SCOPUS
Journal Title
BIOMATERIALS
Volume
101
Start Page
143
End Page
155
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/153944
DOI
10.1016/j.biomaterials.2016.05.052
ISSN
0142-9612
Abstract
Recently, PIWI-interacting small non-coding RNAs (piRNAs) have emerged as novel cancer biomarkers candidate because of their high expression level in various cancer types and role in the control of tumor suppressor genes. In this study, a novel breast cancer theragnostics probe based on a single system targeting the piRNA-36026 (piR-36026) molecular pathway was developed using a piR-36026 molecular beacon (MB). The piR-36026 MB successfully visualized endogenous piR-36026 biogenesis, which is highly expressed in MCF7 cells (a human breast cancer cell line), and simultaneously inhibited piR-36026-mediated cancer progression in vitro and in vivo. We discovered two tumor suppressor proteins, SERPINA1 and LRAT, that were directly regulated as endogenous piR-36026 target genes in MCF7 cells. Furthermore, multiplex bioimaging of a single MCF7 cell following treatment with piR-36026 MB clearly visualized the direct molecular interaction of piRNA-36026 with SERPINAI or LRAT and subsequent molecular therapeutic responses including caspase-3 and PI in the nucleus. Lee, YJ
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