Evidence map›Paper›PMID 26315541›Full record

ArticleOncotarget2015

MicroRNA-424 inhibits Akt3/E2F3 axis and tumor growth in hepatocellular carcinoma.

Hao Yang, Wei Zheng, Xiao Shuai, Rui-Min Chang, Lei Yu, Feng Fang, Lian-Yue Yang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

40 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. miRNAs in pancreatic cancer progression and metastasis.Clinical & experimental metastasis · 2024
    Review
  3. Role of miR-424 in the carcinogenesis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Sequence Requirements for miR-424-5p Regulating and Function in Cancers.International journal of molecular sciences · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Differential expression of angiogenesis-related miRNAs andArchives of medical science : AMS · 2020
    Article
  20. Role of miRNA-424 in Cancers.OncoTargets and therapy · 2020
    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

7 authors at 2 institutions in 1 country.

Hao YangLiver Cancer Laboratory, Xiangya Hospital, Central South University, Changsha 410008, Hunan, China.
Wei ZhengLiver Cancer Laboratory, Xiangya Hospital, Central South University, Changsha 410008, Hunan, China.
Xiao ShuaiLiver Cancer Laboratory, Xiangya Hospital, Central South University, Changsha 410008, Hunan, China.
Rui-Min ChangLiver Cancer Laboratory, Xiangya Hospital, Central South University, Changsha 410008, Hunan, China.
Lei YuLiver Cancer Laboratory, Xiangya Hospital, Central South University, Changsha 410008, Hunan, China.
Feng FangLiver Cancer Laboratory, Xiangya Hospital, Central South University, Changsha 410008, Hunan, China.
Lian-Yue YangLiver Cancer Laboratory, Xiangya Hospital, Central South University, Changsha 410008, Hunan, China.
Central South University · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

By comparing the expression profiles of miRNAs in different subtypes of HCC, we identified miR-424 as a HCC related miRNA. We found that the expression of miR-424 was significantly decreased in HCC tissues and six liver cancer cell lines. Significantly, its expression levels were correlated with tumor size, multiple nodules, vein invasion, TNM stage and overall survival of HCC. We showed that up-regulated miR-424 suppressed HCC cell proliferation in vivo and in vitro. Multi-pathway reporter arrays suggested that miR-424 suppressed the pRb-E2F pathway. Consistently, Akt3 and E2F3 were identified as the targets of miR-424 as evidenced by that ectopic miR-424 expression suppressed Akt3 and E2F3 expressions. Silencing Akt3 and E2F3 by siRNA pheno-copied the effect of ectopic miR-424 on HCC growth. Whereas, overexpression of Akt3 and E2F3 attenuated the effect of miR-424 on HCC growth. Together, our data demonstrated a tumor suppressor role for miR-424 in HCC development and progression with therapeutic implications. The strong correlation of miR-424 expression with HCC patient survival suggests that miR-424 could be a valuable biomarker for HCC prognosis.

Indexed as

Gene Expression Regulation, NeoplasticAgedAnimalsBiomarkers, TumorCarcinoma, HepatocellularCell Line, TumorCell ProliferationCohort StudiesDisease ProgressionE2F3 Transcription FactorFemaleGenes, Tumor SuppressorHumansKi-67 AntigenLiver NeoplasmsMaleAKT3 protein, humanBiomarkers, TumorE2F3 protein, humanE2F3 Transcription FactorKi-67 AntigenMicroRNAsMIRN424 microrna, humanProto-Oncogene Proteins c-aktRNA, Small InterferingAkt3E2F3hepatocellular carcinomamiR-424tumor growth

Identifiers

PMID26315541
PMCPMC4695022
OpenAlexW1733527712

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LicenceCC BY
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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.