Evidence map›Paper›PMID 27899819›Full record

ArticleCell death & disease2016

4-cholesten-3-one suppresses lung adenocarcinoma metastasis by regulating translocation of HMGB1, HIF1α and Caveolin-1.

Jinben Ma, Guobin Fu, Jing Wu, Shaoxian Han, Lishan Zhang, Ming Yang, Yong Yu, Mengyuan Zhang, Yanliang Lin, Yibing Wang

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  10. Frontiers in pharmacology · 2020
    Article
  11. Article
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  13. Article
  14. Effects of purifiedOncology letters · 2018
    Article
  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Jinben MaDepartment of Anesthesiology, Shandong provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Guobin FuDepartment of Oncology, Shandong provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Jing WuDepartment of Anesthesiology, Shandong provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Shaoxian HanDepartment of thoracic surgery, Shandong chest Hospital, Jinan 250021, China.
Lishan ZhangDepartment of Hand and Foot Surgery, Shandong provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Ming YangDepartment of Ultrasound, Shandong provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Yong YuDepartment of Ultrasound, Shandong provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Mengyuan ZhangDepartment of Anesthesiology, Shandong provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Yanliang LinDepartment of Center Laboratory, Shandong provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Yibing WangDepartment of burn and plastic surgery, Shandong provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Shandong University · CNShandong Chest Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastasis is a great challenge in lung adenocarcinoma (ADC) therapy. Cholesterol has been implicated in ADC metastasis. 4-cholesten-3-one, as cholesterol metabolite and analog, can substitute membrane cholesterol and increase membrane fluidity. In this study, we explored the possibility that 4-cholesten-3-one inhibited ADC metastasis. Low-dose 4-cholesten-3-one significantly restrained ADC cells migration and invasion with little effects on cells viabilities. Further investigation showed that 4-cholesten-3-one promoted ROS generation, which transiently activated AMPKα1, increased HIF1α expression, reduced Bcl-2 expression and caused autophagy. AMPKα1 knockdown partly suppressed 4-cholesten-3-one-induced autophagy but, neither prevented 4-cholesten-3-one-induced upregulation of HIF1α or downregulation of Bcl-2. 4-cholesten-3-one-induced autophagy facilitated the release of HMGB1 from nuclei to cytoplasm, blocking nuclear translocation of HIF1α and activation of MMP2 and MMP9. Also, 4-cholesten-3-one induced time-dependent phosphorylation of caveolin-1, Akt and NF-κB. With increasing treatment time, 4-cholesten-3-one accelerated caveolin-1 internalization, but reduced the phosphorylation of Akt and NF-κB, and inhibited the expression of snail and twist. These data suggested that 4-cholesten-3-one could be a potential candidate for anti-metastasis of lung adenocarcinoma.

Indexed as

AdenocarcinomaAdenocarcinoma of LungAnimalsAutophagyBrain NeoplasmsCaveolin 1Cell Line, TumorCell MovementCell ProliferationCell SurvivalCholestenonesCholesterolEndocytosisHMGB1 ProteinHypoxia-Inducible Factor 1, alpha SubunitLung NeoplasmsCaveolin 1cholest-4-en-3-oneCholestenonesCholesterolHMGB1 ProteinHypoxia-Inducible Factor 1, alpha SubunitReactive Oxygen Species

Identifiers

PMID27899819
PMCPMC5059879
OpenAlexW2521362603

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.