Evidence map›Paper›PMID 28074905›Full record

ArticleScientific reports2017

MiR-488 inhibits proliferation and cisplatin sensibility in non-small-cell lung cancer (NSCLC) cells by activating the eIF3a-mediated NER signaling pathway.

Chao Fang, Yi-Xin Chen, Na-Yiyuan Wu, Ji-Ye Yin, Xiang-Ping Li, Hsuan-Shun Huang, Wei Zhang, Hong-Hao Zhou, Zhao-Qian Liu

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
5.0field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 84 citations in OpenAlex.

  1. Trial
  2. Article
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  4. Article
  5. Article
  6. Cisplatin in Liver Cancer Therapy.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Review
  9. Proteomic profiling of eIF3a conditional knockout mice.Frontiers in molecular biosciences · 2023
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Emerging Role of Non-Coding RNAs in Senescence.Frontiers in cell and developmental biology · 2022
    Review
  17. Article
  18. Article
  19. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Chao FangDepartments of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Yi-Xin ChenDepartments of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Na-Yiyuan WuDepartments of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Ji-Ye YinDepartments of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Xiang-Ping LiDepartments of Pharmacy, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Hsuan-Shun HuangDepartment of Research, Cervical Cancer Prevention Center, Tzu Chi University, Hualien 970, Taiwan, Republic of China.
Wei ZhangDepartments of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Hong-Hao ZhouDepartments of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Zhao-Qian LiuDepartments of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Central South University · CNXiangya Hospital Central South University · CNPharmacoGenetics (China) · CNTzu Chi University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our previous studied indicated that eukaryotic translation initiation factor 3a (eIF3a) increases the sensitive of platinum-based chemotherapy in lung cancer. MiRNAs play an important role in lung carcinogenesis and drug response. In this study, we aimed to identify potential endogenous miRNAs that inhibit eIF3a expression and determine their influence of this inhibition on cisplatin resistance. Using bioinformatics analysis prediction and confirmation with dual-luciferase reporter assays, we found that miRNA-488 inhibited eIF3a expression by directly binding to the 3'UTR of eIF3a. In addition, the overexpression of miRNA-488 inhibited cell migration and invasion in A549 cells, and also inhibited cell proliferation, cell cycle progression by elevated P27 expression. Compared to the parental cell line, A549/cisplatin (DDP) resistant cells exhibited a higher level of miRNA-488. Moreover, we found that miRNA-488 was associated with cisplatin resistance in three NSCLC cells (A549, H1299 and SK-MES-1). The mechanism of miRNA-488 induced cisplatin resistance was that miRNA-488 activated nucleotide excision repair (NER) by increasing the expression of Replication Protein A (RPA) 14 and Xeroderma pigmentosum group C (XPC). In conclusion, our results demonstrated that miRNA-488 is a tumor suppressor miRNA that acts by targeting eIF3a. Moreover, miRNA-488 also participates in eIF3a mediated cisplatin resistance in NSCLC cells.

Indexed as

Base SequenceCarcinoma, Non-Small-Cell LungCell Line, TumorCell MovementCell ProliferationCisplatinDNA RepairDrug Resistance, NeoplasmEukaryotic Initiation Factor-3Gene Expression Regulation, NeoplasticHumansLung NeoplasmsMicroRNAsModels, BiologicalNeoplasm InvasivenessSignal TransductionCisplatinEIF3A protein, humanEukaryotic Initiation Factor-3MicroRNAsMIRN488 microRNA, human

Identifiers

PMID28074905
PMCPMC5225486
OpenAlexW2576034792

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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.