Evidence map›Paper›PMID 35524319›Full record

ArticleMolecular cancer2022

M6A-mediated upregulation of circMDK promotes tumorigenesis and acts as a nanotherapeutic target in hepatocellular carcinoma.

Ashuai Du, Shiqin Li, Yuzheng Zhou, Cyrollah Disoma, Yujie Liao, Yongxing Zhang, Zongpeng Chen, Qinglong Yang, Pinjia Liu, Sixu Liu and 10 more

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 155 papers.

0numbers the graph read from it
0cells of the map it votes in
155citing papers in PubMed
19.8field-weighted citation impact, top 1% 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

155 citing papers in PubMed, 241 citations in OpenAlex.

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95 more citing papers are in PubMed but not listed here.

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

20 authors at 3 institutions in 1 country.

Ashuai Du *Department of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Shiqin Li *Department of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Yuzheng ZhouDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Cyrollah DisomaDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Yujie LiaoDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Yongxing ZhangDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Zongpeng ChenDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Qinglong YangDepartment of General Surgery, Guizhou Provincial People's Hospital, Guizhou, 550000, Guiyang, China.
Pinjia LiuDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Sixu LiuDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Zijun DongDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Aroona RazzaqDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Siyi TaoDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Xuan ChenDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Yuxin LiuDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Lunan XuDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Qianjun ZhangInstitute of Reproduction and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, 410078, China.
Shanni LiDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China.
Jian PengDepartment of Geriatric Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
Zanxian XiaDepartment of Cell Biology, School of Life Sciences, Central South University, Tongzipo Road, Changsha, 410013, China. xiazanxian@sklmg.edu.cn.
Central South University · CNGuizhou Provincial People's Hospital · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEmerging evidence suggest the critical role of circular RNAs (circRNAs) in disease development especially in various cancers. However, the oncogenic role of circRNAs in hepatocellular carcinoma (HCC) is still largely unknown.

methodsRNA sequencing was performed to identify significantly upregulated circRNAs in paired HCC tissues and non-tumor tissues. CCK-8 assay, colony formation, transwell, and xenograft mouse models were used to investigate the role of circRNAs in HCC proliferation and metastasis. Small interfering RNA (siRNA) was used to silence gene expression. RNA immunoprecipitation, biotin pull-down, RNA pull-down, luciferase reporter assay and western blot were used to explore the underlying molecular mechanisms.

resultsHsa_circ_0095868, derived from exon 5 of the MDK gene (named circMDK), was identified as a new oncogenic circRNA that was significantly upregulated in HCC. The upregulation of circMDK was associated with the modification of N6-methyladenosine (m

conclusionsCircMDK could serve as a potential tumor biomarker that promotes the progression of HCC via the miR-346/874-3p-ATG16L1 axis. The PAE-based delivery of siRNA improved the stability and efficiency of siRNA targeting circMDK. The PAE-siRNA nanoparticles effectively inhibited HCC proliferation and metastasis in vivo. Our current findings offer a promising nanotherapeutic strategy for the treatment of HCC.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMicroRNAsAnimalsCarcinogenesisCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansMicePhosphatidylinositol 3-KinasesRNA, CircularRNA, Small InterferingUp-RegulationMicroRNAsMIRN346 microRNA, humanMIRN874 microRNA, humanPhosphatidylinositol 3-KinasesRNA, CircularRNA, Small InterferingApoptosisATG16L1circRNAHepatocellular carcinoma (HCC)IGF2BP1N6-methyladenosine (m6A)Nanoparticles (NPs)Poly (β-amino esters) (PAEs)

Identifiers

PMID35524319
PMCPMC9074191
OpenAlexW4229045711

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Registered trials

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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.