Evidence map›Paper›PMID 26942465›Full record

ArticleOncotarget2016

MicroRNA-432 functions as a tumor suppressor gene through targeting E2F3 and AXL in lung adenocarcinoma.

Ling Chen, Guangming Kong, Chuantao Zhang, Hongyan Dong, Cuicui Yang, Guanhua Song, Chengye Guo, Lin Wang, Hongsheng Yu

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 49 citations in OpenAlex.

  1. MicroRNAs as biomarkers and molecular mediators of cognitive dysfunction in schizophrenia.Journal of neural transmission (Vienna, Austria : 1996) · 2026
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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

9 authors at 5 institutions in 1 country.

Ling ChenDepartment of Oncology, Affiliated Hospital of Qingdao University, Qingdao, China.
Guangming KongEmergency Department, Qingdao Municipal Hospital, Qingdao, China.
Chuantao ZhangDepartment of Oncology, Affiliated Hospital of Qingdao University, Qingdao, China.
Hongyan DongDepartment of Pathology, Linyi People's Hospital, Linyi, China.
Cuicui YangDepartment of Pathology, Linyi People's Hospital, Linyi, China.
Guanhua SongInstitute of Basic Medicine, Shandong Academy of Medical Sciences, Jinan, China.
Chengye GuoDepartment of Oncology, Qingdao Municipal Hospital, Qingdao, China.
Lin WangResearch Center for Medicinal Biotechnology, Key Laboratory for Rare and Uncommon Diseases of Shandong Province, Shandong Academy of Medical Sciences, Jinan, China.
Hongsheng YuDepartment of Oncology, Affiliated Hospital of Qingdao University, Qingdao, China.
Affiliated Hospital of Qingdao University · CNLinyi People's Hospital · CNQingdao University · CNShandong First Medical University · CNQingdao Municipal Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abnormal proliferation and drug resistance are the hallmarks of lung adenocarcinoma (LAD). Dispite the advances in diagnosis and therapy, the 5-year survival remains low. Increasing studies regarding its pathological mechanism have been focused on microRNA (miRNA) due to its nodal regulatory properties. This study aims to characterize the expression of miR-432 in LAD and investigate its effects on the proliferation and sensitivity of lung cancer cells to cisplatin. Here, we report that downregulation of miR-432 in LAD tissues was correlated with a higher clinical stage (p = 0.03) and poor prognosis (p = 0.036). Additionally, miR-432 expression was negative correlated with high Ki67 labeling index (p = 0.016) in our cohorts. Functionally, over-expression of miR-432 inhibits cell proliferation through arresting cell cycle and sensitizes tumor cells to cisplatin. Mechanistically, miR-432 functions by directly targeting E2F3 and AXL, and they, in turn, mediate the regulation of miR-432 towards cell proliferation and cisplatin sensitivity. Importantly, miR-432 levels are negatively correlated with the levels of E2F3 and AXL in human LAD tissues. These results demonstrated that miR-432 functions as a tumor-suppressive miRNA and may represent a prognostic parameter and therapeutic target for LAD.

Indexed as

Gene Expression Regulation, NeoplasticAdenocarcinomaAnimalsApoptosisAxl Receptor Tyrosine KinaseBiomarkers, TumorCell ProliferationE2F3 Transcription FactorFemaleFollow-Up StudiesGenes, Tumor SuppressorHumansLung NeoplasmsLymphatic MetastasisMaleMiceAxl Receptor Tyrosine KinaseBiomarkers, TumorE2F3 protein, humanE2F3 Transcription FactorMicroRNAsMIRN432 microRNA, humanProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesAXLE2F3lung adenocarcinomamiR-432

Identifiers

PMID26942465
PMCPMC4991437
OpenAlexW2288880627

What OpenQuestion holds

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LicenceCC BY
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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.