Evidence map›Paper›PMID 30338932›Full record

ArticleJournal of cellular and molecular medicine2019

Liver X receptor activation reduces gastric cancer cell proliferation by suppressing Wnt signalling via LXRβ relocalization.

Qiang Wang, Fan Feng, Jiayou Wang, Meijia Ren, Zhonggang Shi, Xiang Mao, Heng Zhang, Xiaoli Ju

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  11. Statins: a repurposed drug to fight cancer.Journal of experimental & clinical cancer research : CR · 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

8 authors at 2 institutions in 1 country.

Qiang WangInstitute of Life Sciences, Jiangsu University, Zhenjiang, China.ORCID 0000-0003-3123-3889
Fan FengThe Fourth Affiliated Hospital of Jiangsu University, Zhenjiang, China.
Jiayou WangInstitute of Life Sciences, Jiangsu University, Zhenjiang, China.
Meijia RenInstitute of Life Sciences, Jiangsu University, Zhenjiang, China.
Zhonggang ShiSchool of Medicine, Jiangsu University, Zhenjiang, China.
Xiang MaoSchool of Medicine, Jiangsu University, Zhenjiang, China.
Heng ZhangDepartment of General Surgery, Nanjing Lishui District People's Hospital, Zhongda Hospital Lishui Branch, Southeast University, Nanjing, China.
Xiaoli JuSchool of Medicine, Jiangsu University, Zhenjiang, China.
Jiangsu University · CNZhongda Hospital Southeast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver X receptors (LXRs) are involved in various diseases associated with lipid disorders, and in regulating cancer cell proliferation. However, the underlying molecular mechanisms, especially those in gastric cancer (GC) remain to be clarified. In this study, immunohistochemistry analysis revealed that LXRβ was mainly expressed in GC tissue, with less expression in adjacent normal tissues. The LXRβ agonist T0901317 efficiently suppressed the proliferation and colony formation of various GC cell lines. We further showed that LXRβ translocated from the cytoplasm to the nucleus when activated by T0901317. LXRβ nuclear localization suppressed the activation of Wnt signalling and decreased the expression of target genes such as MYC, BMP4, and MMP7 through binding to their promoters. Moreover, we demonstrated that the LXR agonist efficiently suppressed GC tumour growth in a nude mouse xenograft model. Taken together, these results revealed that LXRβ agonist inhibited GC cells proliferation by suppressing Wnt signalling via LXRβ relocalization. The results strongly suggest that LXRβ could be a promising target in GC therapy.

Indexed as

Gene Expression Regulation, NeoplasticAgedAnimalsAnticholesteremic AgentsAntineoplastic AgentsBenzenesulfonamidesBone Morphogenetic Protein 4Cell Line, TumorCell MovementCell NucleusCell ProliferationCytoplasmFemaleFluorocarbonsHumansHydrocarbons, FluorinatedAnticholesteremic AgentsAntineoplastic AgentsBenzenesulfonamidesBMP4 protein, humanBone Morphogenetic Protein 4FluorocarbonsHydrocarbons, FluorinatedLiver X ReceptorsMatrix Metalloproteinase 7MMP7 protein, humanMYC protein, humanProto-Oncogene Proteins c-mycSulfonamidesT0901317cell proliferationgastric cancerLXRβtranslocationWnt signalling

Identifiers

PMID30338932
PMCPMC6349166
OpenAlexW2897565062

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.