Evidence map›Paper›PMID 31883226›Full record

ArticleThoracic cancer2020

MiR-148b suppressed non-small cell lung cancer progression via inhibiting ALCAM through the NF-κB signaling pathway.

Zhe Jiang, JingWen Zhang, FuHui Chen, Yajiao Sun

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-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

14 citing papers in PubMed, 21 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Zhe JiangDepartment of Pulmonary and Critical Care Medicine, The Second Affiliated Hospital of Harbin Medical University, Heilongjiang, China.
JingWen ZhangDepartment of Pulmonary and Critical Care Medicine, The Second Affiliated Hospital of Harbin Medical University, Heilongjiang, China.
FuHui ChenDepartment of Pulmonary and Critical Care Medicine, The Second Affiliated Hospital of Harbin Medical University, Heilongjiang, China.
Yajiao SunDepartment of Pulmonary and Critical Care Medicine, The Second Affiliated Hospital of Harbin Medical University, Heilongjiang, China.ORCID 0000-0003-4643-881X
Harbin Medical University · CN

Funding

National Major Science and Technology Project for the Control and Prevention of Major Infectious Diseases of China 2017ZX10103004Natural Science Foundation of Heilongjiang Province of China LH2019H071
6 · The paper itself

Abstract

backgroundNon-small cell lung cancer (NSCLC) is the leading cause of cancer mortality worldwide. MiRNAs are recognized as important molecules in cancer biology. The aim of the study was to identify a novel biomarker miR-148b and its mechanism in the modulation of NSCLC progression.

methodsThe expressional level of miR-148b was analyzed by RT-PCR. The effect of miR-4317 on proliferation was evaluated through 3-(4,5-Dimethyl-2-thiazolyl)-2,5-diphenyl-2Htetrazolium bromide (MTT) assay. The effect of miR-148b on the metastasis of NSCLC was detected through transwell assays. The verification of the target of miR-148b was assessed by TargetScan and dual-luciferase reporter assay. The related proteins in this study were analyzed by western blot.

resultsOur findings confirmed that miR-148b was decreased in NSCLC and NSCLC patients with lower expression exhibited poorer overall survival (OS). Increasing miR-148b significantly repressed proliferation, invasion and migration. More importantly, activated leukocyte cell adhesion molecule (ALCAM) was determined as the direct target of miR-148b, and reintroduction of ALCAM attenuated miR-148b effect on the progress of NSCLC. In addition, NF-κB signaling pathway was modulated by miR-148b/ALCAM axis.

conclusionsOur results indicated that miR-148b is able to suppress NSCLC growth and metastasis via targeting ALCAM through the NF-κB pathway. These findings provided new evidence that miR-148b serves as a potential biomarker and novel target for NSCLC treatment.

Indexed as

Gene Expression Regulation, NeoplasticActivated-Leukocyte Cell Adhesion MoleculeAntigens, CDApoptosisBiomarkers, TumorCarcinoma, Non-Small-Cell LungCell Adhesion Molecules, NeuronalCell MovementCell ProliferationDisease ProgressionFemaleFetal ProteinsHumansLung NeoplasmsMaleMicroRNAsActivated-Leukocyte Cell Adhesion MoleculeALCAM protein, humanAntigens, CDBiomarkers, TumorCell Adhesion Molecules, NeuronalFetal ProteinsMicroRNAsMIRN148 microRNA, humanNF-kappa BALCAMmiR-148bNF-κBNSCLCprogression

Identifiers

PMID31883226
PMCPMC6997015
OpenAlexW2998281801

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.