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ID 67529
フルテキストURL
fulltext.pdf 1.25 MB
著者
Notomi, Ryotaro Graduate School of Pharmaceutical Sciences, Kyushu University
Sasaki, Shigeki Graduate School of Pharmaceutical Sciences, Nagasaki International University
Taniguchi, Yosuke Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
抄録
Triplex DNA formation is a useful genomic targeting tool that is expected to have a wide range of applications, including the antigene method; however, there are fundamental limitations in its forming sequence. We recently extended the triplex DNA-forming sequence to methylated DNA sequences containing 5mCG base pairs by developing guanidino-dN, which is capable of recognizing a 5mCG base pair with high affinity. We herein investigated the effect of triplex DNA formation using TFOs with guanidino-dN on methylated DNA sequences at the promoter of the RASSF1A gene, whose expression is epigenetically suppressed by DNA methylation in MCF-7 cells, on gene expression. Interestingly, triplex DNA formation increased the expression of the RASSF1A gene at the transcript and protein levels. Furthermore, RASSF1A-activated MCF-7 cells exhibited cell growth suppressing activity. Changes in the expression of various genes associated with the promotion of apoptosis and breast cancer survival accompanied the activation of RASSF1A in cells exhibited antiproliferative activity. These results suggest the potential of increases in gene expression through triplex DNA formation as a new genomic targeting tool.
発行日
2024-07-31
出版物タイトル
RSC Chemical Biology
5巻
9号
出版者
Royal Society of Chemistry
開始ページ
884
終了ページ
890
ISSN
2633-0679
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2024 The Author(s).
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1039/d4cb00134f
ライセンス
https://creativecommons.org/licenses/by/3.0/
助成機関名
Japan Society for the Promotion of Science
Japan Agency for Medical Research and Development
Japan Science and Technology Agency
助成番号
JP23H02610
JP23K27301
JP21am0401026
JPMJSP2136