Evidence map›Paper›PMID 25111230›Full record

ArticleThe American journal of pathology2014

Sphingosine-1-phosphate mediates a reciprocal signaling pathway between stellate cells and cancer cells that promotes pancreatic cancer growth.

Yan Bi, Jiachu Li, Baoan Ji, Ningling Kang, Liu Yang, Douglas A Simonetto, Jung H Kwon, Marielle Kamath, Sheng Cao, Vijay Shah

Open access · hybridAbstract read
In one paragraph

Article in The American journal of pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Role of Sphingosine-1-Phosphate Signaling Pathway in Pancreatic Diseases.International journal of molecular sciences · 2024
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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

10 authors at 3 institutions in 2 countries.

Yan BiGastroenterology Research Unit, the Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Jiachu LiGastroenterology Research Unit, the Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota; Department of Oncology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Baoan JiGastroenterology Research Unit, the Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Ningling KangGastroenterology Research Unit, the Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Liu YangGastroenterology Research Unit, the Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Douglas A SimonettoGastroenterology Research Unit, the Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Jung H KwonGastroenterology Research Unit, the Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Marielle KamathGastroenterology Research Unit, the Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Sheng CaoGastroenterology Research Unit, the Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Vijay ShahGastroenterology Research Unit, the Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota. Electronic address: shah.vijay@mayo.edu.
WinnMed · USMayo Clinic · USFirst Affiliated Hospital of Chongqing Medical University · CN

Funding

Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI Tamas Ordog · 2009 to 2026
$22.2M
Paul Calabresi Program in Clinical/Translational Research at Mayo ClinicK12CA090628 · NCI · MAYO CLINIC ROCHESTER · PI WEROHA, SARAVUT · 2001 to 2025
$19.7M
Molecular Mechanisms of Portal HypertensionR01DK059615 · NIDDK · MAYO CLINIC ROCHESTER · PI SHAH, VIJAY H. · 2002 to 2023
$6.4M
HEPATIC STELLATE CELL REGULATION OF METASTATIC GROWTH IN THE LIVERR01CA160069 · NCI · UNIVERSITY OF MINNESOTA · PI NINGLING KANG · 2011 to 2026
$5.2M
Molecular Mechanisms of Liver Fibrosis (Diversity Supplement)R37AA021171 · NIAAA · MAYO CLINIC ROCHESTER · PI VIJAY H. SHAH · 2019 to 2026
$3.0M
Molecular Mechanisms of Liver FibrosisR01AA021171 · NIAAA · MAYO CLINIC ROCHESTER · PI SHAH, VIJAY H. · 2012 to 2018
$2.5M
Molecular Mechanisms of Portal HypertensionR56DK059615 · NIDDK · MAYO CLINIC ROCHESTER · PI SHAH, VIJAY H · 2007 to 2007
$378k
NCATS NIH HHS UL1 TR000135NCI NIH HHS K12 CA090628NCI NIH HHS K12CA90628NCI NIH HHS R01 CA160069NIAAA NIH HHS AA021171NIAAA NIH HHS R01 AA021171NIAAA NIH HHS R37 AA021171NIDDK NIH HHS DK59615NIDDK NIH HHS P30 DK084567NIDDK NIH HHS P30DK084567NIDDK NIH HHS R01 DK059615NIDDK NIH HHS R56 DK059615
6 · The paper itself

Abstract

Sphingosine-1-phosphate (S1P) is produced by sphingosine kinase 1 and is implicated in tumor growth, although the mechanisms remain incompletely understood. Pancreatic stellate cells (PSCs) reside within the tumor microenvironment and may regulate tumor progression. We hypothesized that S1P activates PSCs to release paracrine factors, which, in turn, increase cancer cell invasion and growth. We used a combination of human tissue, in vitro, and in vivo studies to mechanistically evaluate this concept. Sphingosine kinase 1 was overexpressed in human pancreatic tissue, especially within tumor cells. S1P activated PSCs in vitro and conditioned medium from S1P-stimulated PSCs, increased pancreatic cancer cell migration, and invasion, which was dependent on S1P2, ABL1 (alias c-Abl) kinase, and matrix metalloproteinase-9. In vivo studies showed that pancreatic cancer cells co-implanted with S1P2 receptor knockdown PSCs led to less cancer growth and metastasis in s.c. and orthotopic pancreatic cancer models compared with control PSCs. Pancreatic cancer cell-derived S1P activates PSCs to release paracrine factors, including matrix metalloproteinase-9, which reciprocally promotes tumor cell migration and invasion in vitro and cancer growth in vivo.

Indexed as

Signal TransductionCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansLysophospholipidsMatrix Metalloproteinase 9PancreasPancreatic NeoplasmsPancreatic Stellate CellsPhosphotransferases (Alcohol Group Acceptor)Receptors, LysosphingolipidSphingosineSphingosine KinaseTumor MicroenvironmentUp-RegulationLysophospholipidsMatrix Metalloproteinase 9MMP9 protein, humanPhosphotransferases (Alcohol Group Acceptor)Receptors, LysosphingolipidSphingosinesphingosine 1-phosphateSphingosine Kinase

Identifiers

PMID25111230
PMCPMC4188870
OpenAlexW2060626785

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.