Evidence map›Paper›PMID 35039581›Full record

ArticleScientific reports2022

Targeting of noncoding RNAs encoded by a novel MYC enhancers inhibits the proliferation of human hepatic carcinoma cells in vitro.

Hae In Choi, Ga Yeong An, Eunyoung Yoo, Mina Baek, Jin Choul Chai, Bert Binas, Young Seek Lee, Kyoung Hwa Jung, Young Gyu Chai

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Crosstalk BetweenCancers · 2026
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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 3 institutions in 1 country.

Hae In ChoiDepartment of Bionanotechnology, Hanyang University, Seoul, 04673, Republic of Korea.
Ga Yeong AnDepartment of Bionanotechnology, Hanyang University, Seoul, 04673, Republic of Korea.
Eunyoung YooDepartment of Bionanotechnology, Hanyang University, Seoul, 04673, Republic of Korea.
Mina BaekDepartment of Molecular & Life Science, Hanyang University, Ansan, Gyeonggi-do, 15588, Republic of Korea.
Jin Choul ChaiCollege of Veterinary Medicine, Seoul National University, Seoul, 08826, Republic of Korea.
Bert BinasDepartment of Molecular & Life Science, Hanyang University, Ansan, Gyeonggi-do, 15588, Republic of Korea.
Young Seek LeeCollege of Veterinary Medicine, Seoul National University, Seoul, 08826, Republic of Korea.
Kyoung Hwa JungConvergence Technology Campus of Korea Polytechnic II, Incheon, 21417, Republic of Korea. khjung2@gmail.com.
Young Gyu ChaiDepartment of Bionanotechnology, Hanyang University, Seoul, 04673, Republic of Korea. ygchai@hanyang.ac.kr.
Hanyang University · KRSeoul National University · KRKorea Polytechnic University · KR

Funding

National Research Foundation of Korea 2014M3C9A3064693National Research Foundation of Korea 2016R1D1A1B04934970National Research Foundation of Korea 2017M3A9G7073033National Research Foundation of Korea 2020R1F1A1063217
6 · The paper itself

Abstract

The proto-oncogene MYC is important for development and cell growth, however, its abnormal regulation causes cancer. Recent studies identified distinct enhancers of MYC in various cancers, but any MYC enhancer(s) in hepatocellular carcinoma (HCC) remain(s) elusive. By analyzing H3K27ac enrichment and enhancer RNA (eRNA) expression in cultured HCC cells, we identified six putative MYC enhancer regions. Amongst these, two highly active enhancers, located ~ 800 kb downstream of the MYC gene, were identified by qRT-PCR and reporter assays. We functionally confirmed these enhancers by demonstrating a significantly reduced MYC expression and cell proliferation upon CRISPR/Cas9-based deletion and/or antisense oligonucleotide (ASO)-mediated inhibition. In conclusion, we identified potential MYC enhancers of HCC and propose that the associated eRNAs may be suitable targets for HCC treatment.

Indexed as

RNA, UntranslatedCarcinoma, HepatocellularCell Line, TumorCell ProliferationEnhancer Elements, GeneticGenes, mycHumansLiver NeoplasmsRNA, Untranslated

Identifiers

PMID35039581
PMCPMC8764030
OpenAlexW4206622058

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.