Evidence map›Paper›PMID 34948464›Full record

ArticleInternational journal of molecular sciences2021

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

Yuna Kim, Hyanggi Ji, Eunae Cho, Nok-Hyun Park, Kyeonghwan Hwang, Wonseok Park, Kwang-Soo Lee, Deokhoon Park, Eunsun Jung

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 15 citations in OpenAlex.

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  7. Human Vault RNAs: Exploring Their Potential Role in Cellular Metabolism.International journal of molecular sciences · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Yuna KimBiospectrum Life Science Institute, A-1805, U-TOWER, Yongin-si 16827, Korea.
Hyanggi JiBiospectrum Life Science Institute, A-1805, U-TOWER, Yongin-si 16827, Korea.
Eunae ChoBiospectrum Life Science Institute, A-1805, U-TOWER, Yongin-si 16827, Korea.
Nok-Hyun ParkBasic Research and Innovation Division, Amorepacific Corporation R&D Center, Youngin-si 17074, Korea.
Kyeonghwan HwangBasic Research and Innovation Division, Amorepacific Corporation R&D Center, Youngin-si 17074, Korea.
Wonseok ParkBasic Research and Innovation Division, Amorepacific Corporation R&D Center, Youngin-si 17074, Korea.
Kwang-Soo LeeBiospectrum Life Science Institute, A-1805, U-TOWER, Yongin-si 16827, Korea.
Deokhoon ParkBiospectrum Life Science Institute, A-1805, U-TOWER, Yongin-si 16827, Korea.
Eunsun JungBiospectrum Life Science Institute, A-1805, U-TOWER, Yongin-si 16827, Korea.ORCID 0000-0002-5594-4645
Kolon Life Science (South Korea) · KRAmorepacific (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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-β-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.

Indexed as

DNA MethylationDown-RegulationGenetic MarkersCell ProliferationCells, CulturedCellular SenescenceCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent Kinase Inhibitor p21Epigenesis, GeneticFibroblastsHumansMicroRNAsPlant ExtractsReactive Oxygen SpeciesTeaCDKN1A protein, humanCDKN2A protein, humanCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent Kinase Inhibitor p21Genetic MarkersMicroRNAsMIRN886 microRNA, humanPlant ExtractsReactive Oxygen SpeciesTeaepigenetic regulationfibroblastsgreen tea extractnc886replicative senescence

Identifiers

PMID34948464
PMCPMC8705676
OpenAlexW4200412256

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.