Evidence map›Paper›PMID 26187928›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

MicroRNA-224 promotes tumor progression in nonsmall cell lung cancer.

Ri Cui, Wei Meng, Hui-Lung Sun, Taewan Kim, Zhenqing Ye, Matteo Fassan, Young-Jun Jeon, Bin Li, Caterina Vicentini, Yong Peng and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 2 pooled it
8.1field-weighted citation impact, top 2% 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

91 citing papers in PubMed, 2 syntheses or guidelines pooled it, 170 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. MetaCancerDB: a database of site-specific RNA-miRNA correlations in cancer metastasis.Database : the journal of biological databases and curation · 2026
    Article
  5. Article
  6. Article
  7. A Robust NSCLC Biomarker- miR-7-5p: ItsMicroRNA (Shariqah, United Arab Emirates) · 2025
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Molecular Pathology of Lung Cancer.Cold Spring Harbor perspectives in medicine · 2022
    Review
  18. MiR-590 suppresses the progression of non-small cell lung cancer by regulating YAP1 and Wnt/β-catenin signaling.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Article
  19. Article
  20. Review

31 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 5 institutions in 3 countries.

Ri CuiDepartment of Molecular Virology, Immunology and Medical Genetics and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210; Chemical Biology Research Center, School of Pharmaceutical Sciences and Lung Cancer Research Center, Zhoushan Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325035, China;
Wei MengDepartment of Radiation Oncology and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210;
Hui-Lung SunDepartment of Molecular Virology, Immunology and Medical Genetics and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210;
Taewan KimDepartment of Molecular Virology, Immunology and Medical Genetics and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210;
Zhenqing YeDepartment of Molecular Medicine/Institute of Biotechnology, South Texas Research Facility, The University of Texas Health Science Center at San Antonio, San Antonio, TX 78229-3900;
Matteo FassanApplied Research on Cancer Network (ARC-NET) Research Centre, University of Verona, Verona 37126, Italy;
Young-Jun JeonDepartment of Molecular Virology, Immunology and Medical Genetics and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210;
Bin LiDepartment of Radiation Oncology and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210;
Caterina VicentiniApplied Research on Cancer Network (ARC-NET) Research Centre, University of Verona, Verona 37126, Italy;
Yong PengDepartment of Molecular Virology, Immunology and Medical Genetics and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210;
Tae Jin LeeDepartment of Molecular Virology, Immunology and Medical Genetics and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210;
Zhenghua LuoDepartment of Molecular Virology, Immunology and Medical Genetics and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210;
Lan LiuDepartment of Pathology, Affiliated Hospital of YanBian University, Ji Lin 133002, China;
Dongyuan XuDepartment of Pathology, Affiliated Hospital of YanBian University, Ji Lin 133002, China;
Esmerina TiliDepartment of Molecular Virology, Immunology and Medical Genetics and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210; Department of Anesthesiology, Wexner Medical Center, The Ohio State University, Columbus, OH 43210.
Victor JinDepartment of Molecular Medicine/Institute of Biotechnology, South Texas Research Facility, The University of Texas Health Science Center at San Antonio, San Antonio, TX 78229-3900;
Justin MiddletonDepartment of Molecular Virology, Immunology and Medical Genetics and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210;
Arnab ChakravartiDepartment of Radiation Oncology and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210;
Tim LautenschlaegerDepartment of Radiation Oncology and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210; TimLautenschlaeger01@gmail.com carlo.croce@osumc.edu.
Carlo M CroceDepartment of Molecular Virology, Immunology and Medical Genetics and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210; TimLautenschlaeger01@gmail.com carlo.croce@osumc.edu.
The Ohio State University · USThe University of Texas Health Science Center at San Antonio · USUniversity of Verona · ITThe Ohio State University Wexner Medical Center · USWenzhou Medical University · CN

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
OSU as Network Lead Academic Participating Site for the NCI NCTNU10CA180850 · NCI · OHIO STATE UNIVERSITY · PI BLUM, KRISTIE A, CHAKRAVARTI, ARNAB · 2014 to 2018
$6.8M
Identifying non-coding RNAs for early detection and prevention of lung cancerU01CA166905 · NCI · OHIO STATE UNIVERSITY · PI CROCE, CARLO M, PASS, HARVEY IRA · 2013 to 2017
$4.5M
Novel functions of Pyruvate kinase M2 in DNA double-strand break repairR01CA188500 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI CHAKRAVARTI, ARNAB, XIA, FEN · 2014 to 2019
$2.0M
MiRNAs/UCRs: biomarkers for cancer risk, tumor detection, progression & treatmentU01CA152758 · NCI · OHIO STATE UNIVERSITY · PI CROCE, CARLO M · 2010 to 2014
$1.8M
NCI NIH HHS 1R01CA188500NCI NIH HHS 1U10CA180850-01NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA188500NCI NIH HHS U01 CA152758NCI NIH HHS U01CA152758NCI NIH HHS U01 CA166905NCI NIH HHS U01CA166905NCI NIH HHS U10 CA180850
6 · The paper itself

Abstract

Lung cancer is the leading cause of cancer-related deaths worldwide. Despite advancements and improvements in surgical and medical treatments, the survival rate of lung cancer patients remains frustratingly poor. Local control for early-stage nonsmall cell lung cancer (NSCLC) has dramatically improved over the last decades for both operable and inoperable patients. However, the molecular mechanisms of NSCLC invasion leading to regional and distant disease spread remain poorly understood. Here, we identify microRNA-224 (miR-224) to be significantly up-regulated in NSCLC tissues, particularly in resected NSCLC metastasis. Increased miR-224 expression promotes cell migration, invasion, and proliferation by directly targeting the tumor suppressors TNFα-induced protein 1 (TNFAIP1) and SMAD4. In concordance with in vitro studies, mouse xenograft studies validated that miR-224 functions as a potent oncogenic miRNA in NSCLC in vivo. Moreover, we found promoter hypomethylation and activated ERK signaling to be involved in the regulation of miR-224 expression in NSCLC. Up-regulated miR-224, thus, facilitates tumor progression by shifting the equilibrium of the partially antagonist functions of SMAD4 and TNFAIP1 toward enhanced invasion and growth in NSCLC. Our findings indicate that targeting miR-224 could be effective in the treatment of certain lung cancer patients.

Indexed as

Disease Progression3' Untranslated RegionsAdaptor Proteins, Signal TransducingAnimalsCarcinogenesisCarcinoma, Non-Small-Cell LungCell Line, TumorCell MovementCell ProliferationCpG IslandsDNA MethylationExtracellular Signal-Regulated MAP KinasesGene Expression Regulation, NeoplasticHumansLung NeoplasmsLymphatic Metastasis3' Untranslated RegionsAdaptor Proteins, Signal TransducingExtracellular Signal-Regulated MAP KinasesMicroRNAsMIRN224 microRNA, humanProteinsSmad4 ProteinTNFAIP1 protein, humanmetastasismicroRNANSCLCSMAD4TNFAIP1

Identifiers

PMID26187928
PMCPMC4534291
OpenAlexW1840972770

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.