Evidence map›Paper›PMID 31758653›Full record

ArticleCancer medicine2020

LncRNA LOXL1-AS1 regulates the tumorigenesis and development of lung adenocarcinoma through sponging miR-423-5p and targeting MYBL2.

Wei Li, Biao Zhang, Youchao Jia, Hongyun Shi, Haibo Wang, Qiang Guo, Hefei Li

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed, 31 citations in OpenAlex.

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  10. Soft Tissue Ewing Sarcoma Cell Drug Resistance Revisited: A Systems Biology Approach.International journal of environmental research and public health · 2023
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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

7 authors at 1 institution in 1 country.

Wei LiDepartment of Thoracic Surgery, Affiliated Hospital of Hebei University, Baoding, China.ORCID 0000-0001-9333-2626
Biao ZhangDepartment of Thoracic Surgery, Affiliated Hospital of Hebei University, Baoding, China.
Youchao JiaDepartment of Medical Oncology, Affiliated Hospital of Hebei University, Baoding, China.
Hongyun ShiDepartment of Radiation Oncology, Affiliated Hospital of Hebei University, Baoding, China.
Haibo WangDepartment of Thoracic Surgery, Affiliated Hospital of Hebei University, Baoding, China.
Qiang GuoDepartment of Thoracic Surgery, Affiliated Hospital of Hebei University, Baoding, China.
Hefei LiDepartment of Thoracic Surgery, Affiliated Hospital of Hebei University, Baoding, China.
Affiliated Hospital of Hebei University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung adenocarcinoma (LUAD) is the most common form of malignant tumor and closely correlated with high risk of death worldwide. Accumulating researches have manifested that long noncoding RNAs (lncRNAs) are deeply involved in the progression of multiple cancers. LncRNA LOXL1 antisense RNA 1 (LOXL1-AS1) was identified as an oncogene in several cancers, nonetheless, its biological effect and regulatory mechanism have not been explained in LUAD. Our present study suggested that LOXL1-AS1 expression was considerably increased in LUAD tissues and cells. Moreover, LOXL1-AS1 deficiency notably hampered cell proliferation and migration as well as dramatically facilitated cell apoptosis. Through molecular mechanism assays, LOXL1-AS1 was identified as a cytoplasmic RNA and acted as a sponge of miR-423-5p. Furthermore, MYBL2 was targeted and negatively modified by miR-423-5p. Rescue experiments revealed that MYBL2 knockdown could counteract miR-423-5p repression-mediated enhancement on the progression of LOXL1-AS1 downregulated LUAD cells. More importantly, MYBL2 was discovered to interact with LOXL1-AS1 promoter, indicating a positive feedback loop of LOXL1-AS1/miR-423-5p/MYBL2 in LUAD. These findings manifested the carcinogenic role of LOXL1-AS1 and LOXL1-AS1/miR-423-5p/MYBL2 feedback loop in LUAD, which could be helpful to explore effective therapeutic strategy for LUAD patients.

Indexed as

Gene Expression Regulation, NeoplasticAdenocarcinoma of LungAmino Acid OxidoreductasesBiomarkers, TumorCell Cycle ProteinsCell MovementCell ProliferationCell Transformation, NeoplasticHumansLung NeoplasmsMicroRNAsOligonucleotides, AntisensePrognosisRNA, Long NoncodingTrans-ActivatorsTumor Cells, CulturedAmino Acid OxidoreductasesBiomarkers, TumorCell Cycle ProteinsLOXL1 protein, humanMicroRNAsMIRN423 microRNA, humanMYBL2 protein, humanOligonucleotides, AntisenseRNA, Long NoncodingTrans-ActivatorsLOXL1-AS1lung adenocarcinomamiR-423-5pMYBL2

Identifiers

PMID31758653
PMCPMC6970024
OpenAlexW2990657728

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.