Evidence map›Paper›PMID 35053270›Full record

ArticleBiomolecules2022

Elevated Expression of JMJD5 Protein Due to Decreased miR-3656 Levels Contributes to Cancer Stem Cell-Like Phenotypes under Overexpression of Cancer Upregulated Gene 2.

Natpaphan Yawut, Il-Rae Cho, Phatcharaporn Budluang, Sirichat Kaowinn, Chutima Kaewpiboon, Byeoleun Jeon, Sang-Woo Kim, Ho Young Kang, Min-Kyung Kang, Sang Seok Koh and 1 more

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 48% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. JMJD family proteins in cancer and inflammation.Signal transduction and targeted therapy · 2022
    Review
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

11 authors at 4 institutions in 2 countries.

Natpaphan YawutBK21 Plus, Department of Cogno-Mechatronics Engineering, Optomechatronics Research Center, Pusan National University, Busan 46241, Korea.ORCID 0000-0002-7201-6576
Il-Rae ChoBK21 Plus, Department of Cogno-Mechatronics Engineering, Optomechatronics Research Center, Pusan National University, Busan 46241, Korea.
Phatcharaporn BudluangBK21 Plus, Department of Cogno-Mechatronics Engineering, Optomechatronics Research Center, Pusan National University, Busan 46241, Korea.
Sirichat KaowinnDepartment of General Science and Liberal Arts, Ladkrabang Prince of Chumphon Campus, King Mongkut's Institute of Technology, Chumphon 86160, Thailand.ORCID 0000-0002-5945-917X
Chutima KaewpiboonDepartment of Biology, Faculty of Science, Thaksin University, Patthalung 93210, Thailand.
Byeoleun JeonDepartment of Biological Science, Pusan National University, Busan 46241, Korea.
Sang-Woo KimDepartment of Biological Science, Pusan National University, Busan 46241, Korea.
Ho Young KangDepartment of Microbiology, Pusan National University, Busan 46241, Korea.
Min-Kyung KangDepartment of Biomedical Sciences, Dong-A University, Busan 49315, Korea.
Sang Seok KohDepartment of Biomedical Sciences, Dong-A University, Busan 49315, Korea.
Young-Hwa ChungBK21 Plus, Department of Cogno-Mechatronics Engineering, Optomechatronics Research Center, Pusan National University, Busan 46241, Korea.ORCID 0000-0002-3408-9336
Pusan National University · KRDong-A University · KRKing Mongkut's Institute of Technology Ladkrabang · THThaksin University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of cancer upregulated gene (CUG) 2 induces cancer stem cell-like phenotypes, such as enhanced epithelial-mesenchymal transition, sphere formation, and doxorubicin resistance. However, the precise mechanism of CUG2-induced oncogenesis remains unknown. We evaluated the effects of overexpression of CUG2 on microRNA levels using a microRNA microarray. Levels of miR-3656 were decreased when CUG2 was overexpressed; on the basis of this result, we further examined the target proteins of this microRNA. We focused on Jumonji C domain-containing protein 5 (JMJD5), as it has not been previously reported to be targeted by miR-3656. When CUG2 was overexpressed, JMJD5 expression was upregulated compared to that in control cells. A 3' untranslated region (UTR) assay revealed that an miR-3656 mimic targeted the JMJD5 3'UTR, but the miR-3656 mimic failed to target a mutant JMJD5 3'UTR, indicating that miR-3656 targets the JMJD5 transcript. Administration of the miR-3656 mimic decreased the protein levels of JMD5 according to Western blotting. Additionally, the miR-3656 mimic decreased CUG2-induced cell migration, evasion, and sphere formation and sensitized the cells to doxorubicin. Suppression of JMJD5, with its small interfering RNA, impeded CUG2-induced cancer stem cell-like phenotypes. Thus, overexpression of CUG2 decreases miR-3656 levels, leading to upregulation of JMJD5, eventually contributing to cancer stem cell-like phenotypes.

Indexed as

MicroRNAsNeoplasmsCell Line, TumorChromosomal Proteins, Non-HistoneGene Expression Regulation, NeoplasticNeoplastic Stem CellsPhenotypeSignal TransductionChromosomal Proteins, Non-HistoneMicroRNAscancer stem cellcancer upregulated geneJumonji C domain-containing protein 5miR-3656

Identifiers

PMID35053270
PMCPMC8774111
OpenAlexW4206252451

What OpenQuestion holds

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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.