Evidence map›Paper›PMID 32355517›Full record

ArticleInternational journal of clinical and experimental pathology2020

miR-21 promotes growth, invasion and migration of lung cancer cells by AKT/P-AKT/cleaved-caspase 3/MMP-2/MMP-9 signaling pathway.

Haiquan Li, Jie Zhao, Xiaomin Jia, Yanmin Zhang, Yongliang Du, Huiting Li, Lei Ma, Jian'an Huang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

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  12. Phosphorylation of AGO2 by TBK1 Promotes the Formation of Oncogenic miRISC in NSCLC.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
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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

8 authors at 2 institutions in 1 country.

Haiquan LiDepartment of Respiratory and Critical Care Medicine, First Affiliated Hospital of Soochow University Suzhou, Jiangsu, P. R. China.
Jie ZhaoDepartment of Respiratory Medicine, Second Affiliated Hospital of Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Xiaomin JiaDepartment of Respiratory Medicine, Second Affiliated Hospital of Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Yanmin ZhangDepartment of Respiratory Medicine, Second Affiliated Hospital of Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Yongliang DuDepartment of Respiratory Medicine, Second Affiliated Hospital of Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Huiting LiDepartment of Respiratory Medicine, Second Affiliated Hospital of Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Lei MaDepartment of Respiratory Medicine, Second Affiliated Hospital of Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Jian'an HuangDepartment of Respiratory and Critical Care Medicine, First Affiliated Hospital of Soochow University Suzhou, Jiangsu, P. R. China.
Xuzhou Medical College · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to demonstrate the effects of miR-21 on the growth, migration, and invasion of lung cancer cells A549 in vitro and the possible mechanism.

methodsIn vitro cell migration and invasion potential were determined by Transwell chamber assays. FACS was used to assess the effect of miR-21 on A549 cell cycle and apoptosis. 4-6 week-old female mice were utilized to establish a lung cancer model. The pathologic biopsy was processed by H&E staining. The expression of the proteins PTEN, RECK and Caspase 3 were detected through immunohistochemy and tumor cell apoptosis was measured by TUNEL.

resultsTranswell chamber assays showed that the cells going through the membrane increased significantly compared to the negative control (P<0.05). The tumor volume resulting from miR-21 mimics was significantly greater than in normal mice. Serum ELISA showed that the protein expression levels of MMP-2 and MMP-9 in miR-21 overexpression group were increased significantly. In addition, H&E staining results showed that in miR-21 overexpression tissue, invasion is more severe and immunohistochemical results proved that the miR-21 overexpression group had high expression of Caspase 3 protein but the expression of PTEN and RECK were decreased. TUNEL experiments show that increased the expression of miR-21 can inhibit the apoptosis of tumor cells.

conclusionMicroRNA-21 promotes the proliferation of lung cancer cells and inhibits the apoptosis of lung cancer cells by the AKT/P-AKT/cleaved-caspase 3/MMP-2/MMP-9 signaling pathway.

Indexed as

apoptosisLung cancermigrationmiR-21proliferationsignaling pathway

Identifiers

PMID32355517
PMCPMC7191137
OpenAlexW3023496324

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.