nc886, a Non-Coding RNA, Is a New Biomarker and Epigenetic Mediator of Cellular Senescence in Fibroblasts

被引:12
作者
Kim, Yuna [1 ]
Ji, Hyanggi [1 ]
Cho, Eunae [1 ]
Park, Nok-Hyun [2 ]
Hwang, Kyeonghwan [2 ]
Park, Wonseok [2 ]
Lee, Kwang-Soo [1 ]
Park, Deokhoon [1 ]
Jung, Eunsun [1 ]
机构
[1] Biospectrum Life Sci Inst, A-1805,U TOWER, Yongin 16827, South Korea
[2] Amorepacific Corp R&D Ctr, Basic Res & Innovat Div, Youngin Si 17074, South Korea
关键词
fibroblasts; replicative senescence; epigenetic regulation; nc886; green tea extract; PKR; PHENOTYPE; LNCRNAS;
D O I
10.3390/ijms222413673
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Functional studies of organisms and human models have revealed that epigenetic changes can significantly impact the process of aging. Non-coding RNA (ncRNA), one of epigenetic regulators, plays an important role in modifying the expression of mRNAs and their proteins. It can mediate the phenotype of cells. It has been reported that nc886 (=vtRNA2-1 or pre-miR-886), a long ncRNA, can suppress tumor formation and photo-damages of keratinocytes caused by UVB. The aim of this study was to determine the role of nc886 in replicative senescence of fibroblasts and determine whether substances capable of controlling nc886 expression could regulate cellular senescence. In replicative senescence fibroblasts, nc886 expression was decreased while methylated nc886 was increased. There were changes of senescence biomarkers including SA-beta-gal activity and expression of p16INK4A and p21Waf1/Cip1 in senescent cells. These findings indicate that the decrease of nc886 associated with aging is related to cellular senescence of fibroblasts and that increasing nc886 expression has potential to suppress cellular senescence. AbsoluTea Concentrate 2.0 (ATC) increased nc886 expression and ameliorated cellular senescence of fibroblasts by inhibiting age-related biomarkers. These results indicate that nc886 has potential as a new target for anti-aging and that ATC can be a potent epigenetic anti-aging ingredient.
引用
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页数:11
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