Evidence map›Paper›PMID 31152147›Full record

ArticleOncogene2019

Activation of sphingosine kinase by lipopolysaccharide promotes prostate cancer cell invasion and metastasis via SphK1/S1PR4/matriptase.

Cheng-Fan Lee, Andrew Dang, Elizabeth Hernandez, Rey-Chen Pong, Benjamin Chen, Rajni Sonavane, Ganesh Raj, Payal Kapur, Hsin-Ying Lin, Shang-Ru Wu and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2019. 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
2.7field-weighted citation impact, top 9% 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, 43 citations in OpenAlex.

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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

15 authors at 4 institutions in 2 countries.

Cheng-Fan LeeDepartment of Biochemistry and Molecular Biology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Andrew DangDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Elizabeth HernandezDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Rey-Chen PongDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Benjamin ChenDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Rajni SonavaneDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Ganesh RajDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Payal KapurUrology and Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Hsin-Ying LinDepartment of Biochemistry and Molecular Biology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Shang-Ru WuDepartment of Biochemistry and Molecular Biology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Chun-Jung KoDepartment of Biochemistry and Molecular Biology, College of Medicine, National Taiwan University, Taipei, Taiwan.
U-Ging LoDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Hsin-Yu LeeDepartment of Life Science, National Taiwan University, Taipei, Taiwan.
Jer-Tsong HsiehDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA. jt.hsieh@utsouthwestern.edu.
Ming-Shyue LeeDepartment of Biochemistry and Molecular Biology, College of Medicine, National Taiwan University, Taipei, Taiwan. mslee2006@ntu.edu.tw.ORCID http://orcid.org/0000-0002-8673-5088
The University of Texas Southwestern Medical Center · USNational Taiwan University · TWSouthwestern Medical Center · USThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gram-negative bacteria have been found to be a major population in prostatitis and prostate cancer (PCa) tissues. Lipopolysaccharide (LPS), a major compound of Gram-negative bacteria, with stimulatory activities in some cancer types, but has not been fully studied in PCa. In this study, we examined the effect of LPS on the invasion of PCa cells. Interestingly, LPS can enhance the invasiveness of PCa, but had no significant effect on PCa cell viability. Using protease inhibitor screening and biochemical analyses, matriptase, a member of the membrane-anchored serine protease family, is found to play a key role in LPS-induced PCa cell invasion. Mechanistically, Toll-like receptor 4 (TLR4, LPS receptor)-sphingosine kinase 1 (SphK1) signaling underlies LPS-induced matriptase activation and PCa cell invasion. Specifically, LPS induced the S225 phosphorylation of SphK1 and the translocation of SphK1 to plasma membrane, leading to the production of sphingosine 1-phosphate (S1P), ERK1/2 and matriptase activation via S1P receptor 4 (S1PR4). This phenomenon is further validated using the patient-derived explant (PDE) model. Indeed, there is a significant correlation among the elevated SphK1 levels, the Gleason grades of PCa specimens, and the poor survival of PCa patients. Taken together, this study demonstrates a potential impact of LPS on PCa progression. Our results provide not only a new finding of the role of bacterial infection in PCa progression but also potential therapeutic target(s) associated with PCa metastasis.

Indexed as

Neoplasm InvasivenessNeoplasm MetastasisAdaptor Proteins, Signal TransducingDisease ProgressionEnzyme ActivationHumansMalePhosphotransferases (Alcohol Group Acceptor)PolysaccharidesProstatic NeoplasmsSerine EndopeptidasesSphingosine-1-Phosphate ReceptorsSphingosine KinaseAdaptor Proteins, Signal TransducingmatriptasePhosphotransferases (Alcohol Group Acceptor)PolysaccharidesSerine EndopeptidasesSphingosine-1-Phosphate ReceptorsSphingosine KinaseSPHKAP protein, human

Identifiers

PMID31152147
OpenAlexW2947319503

What OpenQuestion holds

Textmetadata
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.