Evidence map›Paper›PMID 31908488›Full record

ArticleOncoTargets and therapy2019

RNA-Seq Analysis Identified XLOC_009190 as Potential Therapeutic Target for Lung Adenocarcinoma.

Jing Wang, Ning Wang, Wei-Dong Zhao, Li-Xian Zhao, Yong-Guang Jing, Li-Jie Yang, Jie He, Jun Li

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 84% 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

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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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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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 1 institution in 1 country.

Jing Wang *Department of Surgery, School of Clinical Medicine, Dali University, Dali, Yunnan 671000, People's Republic of China.
Ning Wang *Department of Surgery, School of Clinical Medicine, Dali University, Dali, Yunnan 671000, People's Republic of China.
Wei-Dong ZhaoThe First Affiliated Hospital of Dali University, Dali, Yunnan 671000, People's Republic of China.ORCID 0000-0002-7431-2432
Li-Xian ZhaoThe First Affiliated Hospital of Dali University, Dali, Yunnan 671000, People's Republic of China.
Yong-Guang JingDepartment of Human Anatomy, School of Basic Medical Sciences, Dali University, Dali, Yunnan 671000, People's Republic of China.
Li-Jie YangThe First Affiliated Hospital of Dali University, Dali, Yunnan 671000, People's Republic of China.
Jie HeThe First Affiliated Hospital of Dali University, Dali, Yunnan 671000, People's Republic of China.
Jun LiDepartment of Surgery, School of Clinical Medicine, Dali University, Dali, Yunnan 671000, People's Republic of China.
Dali University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe abnormal regulation on the expression of lncRNAs had been linked to multiple kinds of cancers, including lung adenocarcinoma.

methodsIn this study, we carried out RNA-Seq on the three tumors and their paired normal samples from Chinese patients with lung adenocarcinoma. All the transcripts were de novo assembled, among which all the possible lncRNAs were predicted by tools including PLEK, CNCI, CPC, Blastp, hmmscan, and so forth. Their expression levels, altogether with the annotated mRNAs, were quantified. The weighted correlation network analysis and analysis of differential expression were carried out to explain the biological function of these novel lncRNAs.

resultsThe weighted correlation network analysis showed that the lncRNAs, which were highly correlated with protein-coding genes, participated in various pathways, including PI3K kinase pathways. These lncRNAs were important regulators in biological processes. Next, the differentially expressed lncRNAs were identified, including four known lncRNAs and one novel lncRNA (XLOC_009190). The cis-regulation of this novel lncRNA might act on MGST1, which protected cells by conjugation and glutathione peroxidase functions. The trans-regulation of this lncRNA was investigated by its correlated mRNAs. The results showed that it possibly played a role in transmembrane receptors like G protein-coupled receptors and potassium channels.

conclusionWe proposed the potential biological function of XLOC_009190, but further experiments are needed to elucidate its roles and its potential to be the therapeutic target.

Indexed as

de novo assemblylncRNAslung adenocarcinomaRNA-Seq

Identifiers

PMID31908488
PMCPMC6927261
OpenAlexW2995305815

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