Evidence map›Paper›PMID 33228740›Full record

ArticleJournal of experimental & clinical cancer research : CR2020

Up-regulation of VANGL1 by IGF2BPs and miR-29b-3p attenuates the detrimental effect of irradiation on lung adenocarcinoma.

Chun-Cheng Hao, Cui-Yang Xu, Xin-Yu Zhao, Jia-Ning Luo, Gang Wang, Li-Hong Zhao, Xiaofeng Ge, Xiao-Feng Ge

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 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

8 authors at 2 institutions in 1 country.

Chun-Cheng HaoDepartment of Radiotherapy, Harbin Medical University Cancer Hospital, No. 150 Haping Road, Nangang District, 150040, Harbin City, Heilongjiang, China.
Cui-Yang XuDepartment of Radiotherapy, Harbin Medical University Cancer Hospital, No. 150 Haping Road, Nangang District, 150040, Harbin City, Heilongjiang, China.
Xin-Yu ZhaoDepartment of Radiotherapy, Harbin Medical University Cancer Hospital, No. 150 Haping Road, Nangang District, 150040, Harbin City, Heilongjiang, China.
Jia-Ning LuoDepartment of Radiotherapy, Harbin Medical University Cancer Hospital, No. 150 Haping Road, Nangang District, 150040, Harbin City, Heilongjiang, China.
Gang WangDepartment of Radiotherapy, Harbin Medical University Cancer Hospital, No. 150 Haping Road, Nangang District, 150040, Harbin City, Heilongjiang, China.
Li-Hong ZhaoDepartment of Radiotherapy, Harbin Medical University Cancer Hospital, No. 150 Haping Road, Nangang District, 150040, Harbin City, Heilongjiang, China.
Xiaofeng GeDepartment of Radiotherapy, Harbin Medical University Cancer Hospital, No. 150 Haping Road, Nangang District, 150040, Harbin City, Heilongjiang, China.
Xiao-Feng GeDepartment of Radiotherapy, Harbin Medical University Cancer Hospital, No. 150 Haping Road, Nangang District, 150040, Harbin City, Heilongjiang, China. gexiaofeng1211@163.com.
Harbin Medical University · CNThird Affiliated Hospital of Harbin Medical University · CN

Funding

Foundation of Heilongjiang National Health and Family Planning Commission 2017-119Heilongjiang Postdoctoral Fund LBH-Z16099Natural Science Foundation for the Returned Scholars of Heilongjiang Province LC2017039
6 · The paper itself

Abstract

Accumulating evidence suggests that radiation treatment causes an adaptive response of lung adenocarcinoma (LUAD), which in turn attenuates the lethal effect of the irradiation. Previous microarray assays manifested the change of gene expression profile after irradiation. Bioinformatics analysis of the significantly changed genes revealed that VANGL1 may notably influence the effect of radiation on LUAD. To determine the role of VANGL1, this study knocked down or overexpressed VANGL1 in LUAD. M6A level of VANGL1 mRNA was determined by M6A-IP-qPCR assay. Irradiation caused the up-regulation of VANGL1 with the increase of VANGL1 m6A level. Depletion of m6A readers, IGF2BP2/3, undermined VANGL1 mRNA stability and expression upon irradiation. miR-29b-3p expression was decreased by irradiation, however VANGL1 is a target of miR-29b-3p which was identified by Luciferase report assay. The reduction of miR-29b-3p inhibited the degradation of VANGL1 mRNA. Knockdown of VANGL1 enhanced the detrimental effect of irradiation on LUAD, as indicated by more severe DNA damage and increased percentage of apoptotic cells. Immunocoprecipitation revealed the interaction between VANGL1 with BRAF. VANGL1 increased BRAF probably through suppressing the protein degradation, which led to the increase of BRAF downstream effectors, TP53BP1 and RAD51. These effectors are involved in DNA repair after the damage. In summary, irradiation caused the up-regulation of VANGL1, which, in turn, mitigated the detrimental effect of irradiation on LUAD by protecting DNA from damage probably through activating BRAF/TP53BP1/RAD51 cascades. Increased m6A level of VANGL1 and reduced miR-29b-3p took the responsibility of VANGL1 overexpression upon irradiation.

Indexed as

AdenineAdenocarcinoma of LungAdultAgedCarrier ProteinsDNA DamageHumansInsulin-Like Growth Factor Binding Protein 3Lung NeoplasmsMembrane ProteinsMicroRNAsMiddle AgedRNA-Binding ProteinsRNA, MessengerUp-Regulation6-methyladenineAdenineCarrier ProteinsIGF2BP2 protein, humanIGFBP3 protein, humanInsulin-Like Growth Factor Binding Protein 3Membrane ProteinsMicroRNAsMIRN29a microRNA, humanRNA-Binding ProteinsRNA, MessengerVANGL1 protein, human

Identifiers

PMID33228740
PMCPMC7687693
OpenAlexW3108846728

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.