Evidence map›Paper›PMID 30230945›Full record

ArticleCancer biology & therapy2018

MicroRNA-886-3P functions as a tumor suppressor in small cell lung cancer.

Jie Shen, Wei Zhou, Nan Bi, Yong-Mei Song, Fu-Quan Zhang, Qi-Min Zhan, Lv-Hua Wang

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Non-coding 886 (Epigenetics · 2024
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  3. The small noncoding RNARNA (New York, N.Y.) · 2024
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  4. The small non-coding RNAbioRxiv : the preprint server for biology · 2024
    Article
  5. Non-Coding RNAs as Key Regulators in Lung Cancer.International journal of molecular sciences · 2023
    Review
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  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
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  17. 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.

Jie Shena Department of Radiation Oncology , Peking Union Medical College Hospital , Beijing , China.
Wei Zhoub State Key Laboratory of Molecular Oncology , Peking Union medical College Hospital Cancer Hospital, Chinese Academy of Medical Sciences , Beijing , China.
Nan Bic Department of Radiation Oncology , Peking Union medical College Hospital Cancer Hospital, Chinese Academy of Medical Sciences , Beijing , China.
Yong-Mei Songb State Key Laboratory of Molecular Oncology , Peking Union medical College Hospital Cancer Hospital, Chinese Academy of Medical Sciences , Beijing , China.
Fu-Quan Zhanga Department of Radiation Oncology , Peking Union Medical College Hospital , Beijing , China.
Qi-Min Zhanb State Key Laboratory of Molecular Oncology , Peking Union medical College Hospital Cancer Hospital, Chinese Academy of Medical Sciences , Beijing , China.
Lv-Hua Wangc Department of Radiation Oncology , Peking Union medical College Hospital Cancer Hospital, Chinese Academy of Medical Sciences , Beijing , China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNPeking Union Medical College Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small cell lung cancer (SCLC) is a highly aggressive disease and miRNAs may play an important role in modulating SCLC progression. We have previously screened 924 miRNAs and found that miR-886-3P was negatively associated with SCLC survival. In the current study, we further investigated the role of miR-886-3P mimic in regulating SCLC cell phenotypic alteration in vitro and xenograft tumor formation in vivo. We found that transfection of miR-886-3P mimic significantly inhibited SCLC cell proliferation, migration, and colony formation, and induced mesenchymal-epithelial transition (MET) by suppressing TGF-ß1 synthesis in vitro. Furthermore, intra-tumor injection of miR-886-3P mimic lead to necrosis and suppression of tumor invasion to the surrounding tissue in the subcutaneous xenograft tumor, and intra-vein injection of miR-886-3P mimic suppressed xenograft lung cancer growth in vivo. These findings suggested that miR-886-3P functions as a tumor suppressor in SCLC and thus, it might be a potential therapeutic molecule in the treatment of lung cancer.

Indexed as

Gene Expression Regulation, NeoplasticGenes, Tumor SuppressorRNA Interference3' Untranslated RegionsAnimalsCell Line, TumorCell MovementCell ProliferationDisease Models, AnimalEpithelial-Mesenchymal TransitionGene ExpressionGenes, ReporterHumansImmunohistochemistryLung NeoplasmsMice3' Untranslated RegionsMicroRNAsMIRN886 microRNA, humanTGFB1 protein, humanTransforming Growth Factor beta1aggressive diseasecancer biologyfetal bovine serummiR-886-3PmiRNAspGL3-luciferaseSmall cell lung cancerTGF-ß1

Identifiers

PMID30230945
PMCPMC6301808
OpenAlexW2890642725

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.