Evidence map›Paper›PMID 37510314›Full record

ArticleGenes2023

Human Endogenous Retrovirus-H-Derived miR-4454 Inhibits the Expression of

Eun Gyung Park, Du Hyeong Lee, Woo Ryung Kim, Yun Ju Lee, Woo Hyeon Bae, Jung-Min Kim, Hae Jin Shin, Hongseok Ha, Joo Mi Yi, Ssang Goo Cho and 5 more

Open access · goldAbstract read
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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

15 authors at 7 institutions in 1 country.

Eun Gyung ParkDepartment of Integrated Biological Sciences, Pusan National University, Busan 46241, Republic of Korea.ORCID 0000-0002-9575-7043
Du Hyeong LeeDepartment of Integrated Biological Sciences, Pusan National University, Busan 46241, Republic of Korea.
Woo Ryung KimDepartment of Integrated Biological Sciences, Pusan National University, Busan 46241, Republic of Korea.
Yun Ju LeeDepartment of Integrated Biological Sciences, Pusan National University, Busan 46241, Republic of Korea.
Woo Hyeon BaeDepartment of Integrated Biological Sciences, Pusan National University, Busan 46241, Republic of Korea.
Jung-Min KimDepartment of Integrated Biological Sciences, Pusan National University, Busan 46241, Republic of Korea.
Hae Jin ShinDepartment of Integrated Biological Sciences, Pusan National University, Busan 46241, Republic of Korea.
Hongseok HaDivision of Life Sciences, Korea University, Seoul 02841, Republic of Korea.
Joo Mi YiDepartment of Microbiology and Immunology, Inje University College of Medicine, Busan 47392, Republic of Korea.
Ssang Goo ChoDepartment of Stem Cell & Regenerative Biotechnology, Institute of Advanced Regenerative Science, Konkuk University, Seoul 05029, Republic of Korea.ORCID 0000-0002-0968-7932
Yung Hyun ChoiDepartment of Biochemistry, College of Korean Medicine, Dong-Eui University, Busan 47227, Republic of Korea.ORCID 0000-0002-1454-3124
Sun Hee LeemDepartment of Biological Science, Dong-A University, Busan 49315, Republic of Korea.
Hee Jae ChaDepartment of Parasitology and Genetics, College of Medicine, Kosin University, Busan 49104, Republic of Korea.ORCID 0000-0002-6963-2685
Sang Woo KimDepartment of Biological Sciences, College of Natural Sciences, Pusan National University, Busan 46241, Republic of Korea.
Heui Soo KimInstitute of Systems Biology, Pusan National University, Busan 46241, Republic of Korea.
Pusan National University · KRDong-A University · KRDong-Eui University · KRInje University · KRKonkuk University · KRKorea University · KRKosin University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although most human endogenous retroviruses (HERVs) have been silenced and lost their ability to translocate because of accumulated mutations during evolution, they still play important roles in human biology. Several studies have demonstrated that HERVs play pathological roles in numerous human diseases, especially cancer. A few studies have revealed that long non-coding RNAs that are transcribed from HERV sequences affect cancer progression. However, there is no study on microRNAs derived from HERVs related to cancer. In this study, we identified 29 microRNAs (miRNAs) derived from HERV sequences in the human genome. In particular, we discovered that miR-4454, which is HERV-H-derived miRNA, was upregulated in non-muscle-invasive bladder cancer (NMIBC) cells. To figure out the effects of upregulated miR-4454 in NMIBC, genes whose expression was downregulated in NMIBC, as well as tumor suppressor genes, were selected as putative target genes of miR-4454. The dual-luciferase assay was used to determine the negative relationship between miR-4454 and its target genes,

Indexed as

Endogenous RetrovirusesMicroRNAsNon-Muscle Invasive Bladder NeoplasmsUrinary Bladder NeoplasmsGenome, HumanHSP40 Heat-Shock ProteinsHumansTumor Suppressor ProteinsDNAJB4 protein, humanHSP40 Heat-Shock ProteinsMicroRNAsMIRN4454 microRNA, humanSASH1 protein, humanTumor Suppressor ProteinsDnaJ heat shock protein family (Hsp40) member B4HERV-H-derived microRNAshuman endogenous retrovirusmiR-4454miRNAs derived from transposable elementsnon-muscle-invasive bladder cancerSAM and SH3 domain containing 1

Identifiers

PMID37510314
PMCPMC10379226
OpenAlexW4383818572

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.