Evidence map›Paper›PMID 30549035›Full record

ArticleJournal of cellular physiology2019

Ornithine aminotransferase promoted the proliferation and metastasis of non-small cell lung cancer via upregulation of miR-21.

Yanfeng Liu, Lei Wu, Kai Li, Fengrui Liu, Li Wang, Dongling Zhang, Jing Zhou, Xuan Ma, Shengyu Wang, Shuanying Yang

Abstract read
In one paragraph

Article in Journal of cellular physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

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  12. Rational Design, Synthesis, and Mechanism of (3Journal of the American Chemical Society · 2022
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  15. Remarkable and Unexpected Mechanism for (Journal of the American Chemical Society · 2021
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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

10 authors at 2 institutions in 1 country.

Yanfeng LiuDepartment of Respiratory Medicine, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Lei WuDepartment of Medical Affairs, The First Affiliated Hospital of Xi'an Medical University, Xi'an, China.
Kai LiDepartment of Emergency, The First Affiliated Hospital of Xi'an Medical University, Xi'an, China.
Fengrui LiuDepartment of Emergency, The First Affiliated Hospital of Xi'an Medical University, Xi'an, China.
Li WangDepartment of Emergency, The First Affiliated Hospital of Xi'an Medical University, Xi'an, China.
Dongling ZhangDepartment of Emergency, The First Affiliated Hospital of Xi'an Medical University, Xi'an, China.
Jing ZhouDepartment of Respiratory Medicine, The First Affiliated Hospital of Xi'an Medical University, Xi'an, China.
Xuan MaDepartment of Respiratory Medicine, The First Affiliated Hospital of Xi'an Medical University, Xi'an, China.
Shengyu WangDepartment of Respiratory Medicine, The First Affiliated Hospital of Xi'an Medical University, Xi'an, China.
Shuanying YangDepartment of Respiratory Medicine, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.ORCID 0000-0002-9676-9302
Xi'an Medical University · CNSecond Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The incidence and mortality of lung cancer ranked the first among all types of cancer in China, and non-small cell lung cancer (NSCLC) is the most common type of lung cancer accounting for 85% of all lung cancers. Given that the survival rate of patients with advanced NSCLC is still poor nowadays, identification of novel therapeutic targets and the development of effective therapies are desired for the treatment of NSCLC in clinics. In this study, we reported the upregulation of ornithine aminotransferase (OAT) in NSCLC cells and clinical tumor samples as well as its association with the advanced TNM stage, metastasis, and poor tumor differentiation of lung cancer. Using different NSCLC cell lines, we demonstrated that OAT promoted the proliferation, invasion, and migration, inhibited the apoptosis, and altered cell cycle of NSCLC cells; besides, the involvement of OAT-miR-21-glycogen synthase kinase-3β signaling in the functional role of OAT in NSCLC was also revealed. Importantly, in the absence of OAT, the growth and metastasis of tumor lung cancer xenograft was significantly suppressed in the nude mice. Based on our findings, OAT may be a potential novel biomarker for the diagnosis and therapeutic outcome monitoring of NSCLC. Inhibition of OAT may also represent a new therapeutic strategy of NSCLC.

Indexed as

AdultAgedAnimalsCarcinoma, Non-Small-Cell LungCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansLung NeoplasmsMaleMice, Inbred BALB CMice, NudeMicroRNAsMiddle AgedMicroRNAsMIRN21 microRNA, humanMIRN21 microRNA, mouseOrnithine-Oxo-Acid TransaminaseGSK-3βinvasion and migrationmiR-21non-small cell lung cancerornithine aminotransferaseproliferation

Identifiers

PMID30549035
PMCPMC13483213
OpenAlexW2904345087

What OpenQuestion holds

Textmetadata
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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.