Evidence map›Paper›PMID 33978320›Full record

ArticleCancer medicine2021

MiR-3130-5p is an intermediate modulator of 2q33 and influences the invasiveness of lung adenocarcinoma by targeting NDUFS1.

Juan Zhan, Shenghua Sun, Yixing Chen, Chaoqun Xu, Qinwei Chen, Minjie Li, Yihua Pei, Qiyuan Li

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  6. Article
  7. Review
  8. The combination of NDUFS1 with CD4Frontiers in cell and developmental biology · 2023
    Article
  9. Article
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  11. Article
  12. Article
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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 4 institutions in 1 country.

Juan ZhanDepartment of Pulmonary and Critical Care Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-2535-0811
Shenghua SunDepartment of Pulmonary and Critical Care Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Yixing ChenLaboratory, Xiamen Cancer Center, The First Affiliated Hospital of Xiamen University, Xiamen, China.
Chaoqun XuNational Institute for Data Science in Health and Medicine, School of Medicine, Xiamen University, Xiamen, China.
Qinwei ChenNational Institute for Data Science in Health and Medicine, School of Medicine, Xiamen University, Xiamen, China.
Minjie LiDepartment of Thoracic Surgery, Zhongshan Hospital, Xiamen University, Xiamen, China.
Yihua PeiCentral Laboratory, Zhongshan Hospital, Xiamen University, Xiamen, China.
Qiyuan LiNational Institute for Data Science in Health and Medicine, School of Medicine, Xiamen University, Xiamen, China.ORCID 0000-0002-8934-8948
Xiamen University · CNCentral South University · CNZhongshan Hospital of Xiamen University · CNFirst Affiliated Hospital of Xiamen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome-wide association studies (GWAS) have reported a handful of loci associated with lung cancer risk, of which the pathogenic pathways are largely unknown. We performed cis-expression quantitative trait loci (eQTL) mapping for 376 lung cancer related GWAS loci in 227 TCGA lung adenocarcinoma (LUAD) and reported two risk loci as eQTL of miRNA. Among the miRNAs in association with lung cancer risk, we further predicted and validated miR-3130-5p as an intermediate modulator of risk loci 2q33 and the tumor suppressor NDUFS1. We assessed the phenotypic impacts of the interaction between miR-3130-5p and NDUFS1 in both lung cancer cell lines and mice xenograft models. As a result, miR-3130-5p directly regulates the expression of NDUFS1 and the corresponding tumor invasiveness, migration and epithelial-mesenchymal transition (EMT). Our findings provide important clues for the pathogenic mechanism of 2q33 in lung carcinogenesis which informs clinical diagnosis and prognosis of LUAD. We performed a cis-eQTL analysis for 376 lung cancer risk loci based on the expression profiles of 251 miRNAs in a cohort of 227 TCGA lung adenocarcinoma. We report a novel pathogenic pathway of 2q33 via miR-3130-5p and NDUFS1.

Indexed as

Chromosomes, Human, Pair 1Adenocarcinoma of LungAnimalsCell Line, TumorCell MovementEpithelial-Mesenchymal TransitionGenes, Tumor SuppressorGenome-Wide Association StudyHeterograftsHumansLung NeoplasmsMiceMice, Inbred BALB CMice, NudeMicroRNAsNADH DehydrogenaseMicroRNAsMIRN3130 microRNA, humanNADH DehydrogenaseNDUFS1 protein, humanTumor Suppressor Proteins2q33expression quantitative trait locilung adenocarcinoma risk locimiR-3130-5pNDUFS1

Identifiers

PMID33978320
PMCPMC8178510
OpenAlexW3163143385

What OpenQuestion holds

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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.