Evidence map›Paper›PMID 31101115›Full record

ArticleBMC veterinary research2019

Significance of sphingosine kinase 1 expression in feline mammary tumors.

Yi-Chih Chang, Hsiao-Li Chuang, Ji-Hang Yin, Jiunn-Wang Liao, Ter-Hsin Chen, Yu-Chih Wang

Open access · goldAbstract read
In one paragraph

Article in BMC veterinary research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Identifying novel sphingosine kinase 1 inhibitors as therapeutics against breast cancer.Journal of enzyme inhibition and medicinal chemistry · 2020
    Article
  5. Article
  6. Article
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

6 authors at 3 institutions in 1 country.

Yi-Chih ChangDepartment of Biotechnology, College of Medical and Health Science, Asia University, Taichung, Taiwan.
Hsiao-Li ChuangNational Laboratory Animal Center, National Applied Research Laboratories, Taipei, Taiwan.
Ji-Hang YinGraduate Institute of Veterinary Pathobiology, National Chung Hsing University, Yu-Chih Wang, 145 Xingda Rd., South Dist, Taichung City, 402, Taiwan.
Jiunn-Wang LiaoGraduate Institute of Veterinary Pathobiology, National Chung Hsing University, Yu-Chih Wang, 145 Xingda Rd., South Dist, Taichung City, 402, Taiwan.
Ter-Hsin ChenGraduate Institute of Veterinary Pathobiology, National Chung Hsing University, Yu-Chih Wang, 145 Xingda Rd., South Dist, Taichung City, 402, Taiwan.
Yu-Chih WangGraduate Institute of Veterinary Pathobiology, National Chung Hsing University, Yu-Chih Wang, 145 Xingda Rd., South Dist, Taichung City, 402, Taiwan. ycw2017@email.nchu.edu.tw.ORCID http://orcid.org/0000-0003-0144-1388
National Chung Hsing University · TWAsia University · TWNational Institutes of Applied Research · TW

Funding

Ministry of Science and Technology, Taiwan MOST106-2313-B-005 -059 - and MOST107-2311-B-005 -011 -MY3
6 · The paper itself

Abstract

backgroundSphingosine kinase 1 (SPHK1) is an enzyme that converts pro-apoptotic ceramide and sphingosine into anti-apoptotic sphingosine-1-phosphate. There is growing evidence that SPHK1 activation promotes oncogenic transformation, tumor growth, chemotherapy resistance, and metastatic spread. High SPHK1 expression has been associated with a poor prognosis in several human cancers.

resultsIn the present study, the expression level of SPHK1 was examined in feline mammary tumor (FMT) specimens, and the IHC expression level of SPHK1 was associated with the histological grade of FMTs. IHC analysis of 88 FMT cases revealed that the expression level of SPHK1 was upregulated in 53 tumor tissues (60.2%) compared to adjacent mammary tissues. SPHK1 expression in FMTs was significantly associated with histological grade, presence of lymphovascular invasion, and estrogen receptor negativity. Treatment of primary FMT cells with SPHK1 inhibitors reduced cell viability, indicating that SPHK1 acts to promote FMT cell survival. These results indicate that SPHK1 may play an important role in FMTs and may be a therapeutic target in cats with FMT.

conclusionsSPHK1 over-expression in breast cancer tissues is associated with a poor prognosis in humans. SPHK1 over-expression in more aggressive FMTs provides support for a potential role of SPHK1 inhibitors for the treatment of FMTs. Targeting SPHK1 has potent cytotoxic effects in primary FMT cells. These findings suggest that further examination of the role SPHK1 plays in FMTs will pave the way for the investigation of SPHK1 inhibitors in future clinical applications.

Indexed as

AnimalsBlood VesselsCat DiseasesCatsFemaleGene Expression Regulation, NeoplasticLymphatic SystemMammary Glands, AnimalMammary Neoplasms, AnimalNeoplasm InvasivenessPhosphotransferases (Alcohol Group Acceptor)Receptors, EstrogenSphingosine KinasePhosphotransferases (Alcohol Group Acceptor)Receptors, EstrogenSphingosine KinaseFeline mammary tumorSPHK1 - comparative oncology

Identifiers

PMID31101115
PMCPMC6525354
OpenAlexW2947413145

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.