Evidence map›Paper›PMID 28713980›Full record

ArticleMolecular medicine reports2017

miRNA‑1284 inhibits cell growth and induces apoptosis of lung cancer cells.

Jie Li, Hairong Jin, Hua Yu, Bin Wang, Jian Tang

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2017. 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
1.6field-weighted citation impact, top 18% 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, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Plasma microRNA Profiling in Type 2 Diabetes Mellitus: A Pilot Study.International journal of molecular sciences · 2023
    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

5 authors at 2 institutions in 1 country.

Jie LiDepartment of Thoracic Surgery, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Hairong JinDepartment of Thoracic Surgery, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Hua YuDepartment of Thoracic Surgery, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Bin WangDepartment of Thoracic Surgery, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Jian TangDepartment of Cardio‑Thoracic Surgery, First Affiliated Hospital of Chinese PLA General Hospital, Beijing 100048, P.R. China.
Chinese PLA General Hospital · CNFirst Affiliated Hospital of Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is the most common cancer worldwide, and morbidity and mortality associated with lung cancer has been increasing annually in recent decades. MicroRNAs (miRNAs), which are short non‑coding RNA sequences that are involved in the regulation of gene expression, have been previously demonstrated to be key regulators in cancer. The present study aimed to clarify the role of miRNA (miR)‑1284 in lung cancer. A549 lung carcinoma cells were transfected with miR‑1284 mimic or miR‑1284 inhibitor using Lipofectamine 2000. Subsequently, cell viability, growth and apoptosis of A459 cells in the miR‑1284 mimic, miR‑1284 inhibitor and control groups were assayed by MTT assay, bromodeoxyuridine assay and flow cytometry, respectively. Furthermore, the protein expression levels of p27, p21, Bax, pro‑caspase‑3, activated caspase‑3 and Myc were detected by western blot analysis to investigate the molecular mechanisms underlying the effect of miR‑1284 on A549 cells. The cell viability and growth of A549 cells were significantly decreased in the miR‑1284 mimic group compared with the control group, whereas the percentage of apoptotic cells was significantly increased. By contrast, miR‑1284 inhibitor transfection significantly increased the cell viability and growth compared with control, and decreased apoptosis. Furthermore, expression of p27 was increased in miR‑1284 mimic‑transfected A549 cells compared with the control group, whereas p21 was unaffected by miR‑1284 overexpression or inhibition. The expression of Myc was decreased by miR‑1284 mimic transfection compared with the control group. For the other apoptosis‑associated proteins that were investigated (Bax, pro‑caspase‑3 and active caspase‑3), the expression levels in the miR‑1284 mimic transfected cells were higher than in the other two groups (control and miR‑1284 inhibitor). In conclusion, the results suggest that miR‑1284 affects cell proliferation and apoptosis of lung cancer cells, indicating that miR‑1284 may have a key role in lung tumorigenesis.

Indexed as

A549 CellsApoptosisCell ProliferationCell SurvivalFluorescent Antibody TechniqueHumansLung NeoplasmsMicroRNAsProto-Oncogene Proteins c-mycMicroRNAsMIRN1284 microRNA, humanProto-Oncogene Proteins c-myc

Identifiers

PMID28713980
PMCPMC5547959
OpenAlexW2734674739

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.