Evidence map›Paper›PMID 30787172›Full record

ArticleMolecular cancer therapeutics2019

Inhibition of Sphingosine Phosphate Receptor 1 Signaling Enhances the Efficacy of VEGF Receptor Inhibition.

Anthony S Fischl, Xiaoen Wang, Beverly L Falcon, Rowena Almonte-Baldonado, Diane Bodenmiller, Glenn Evans, Julie Stewart, Takako Wilson, Philip Hipskind, Jason Manro and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. S1PR1 suppresses lung adenocarcinoma progression through p-STAT1/miR-30c-5 p/FOXA1 pathway.Journal of experimental & clinical cancer research : CR · 2024
    Article
  3. Review
  4. Article
  5. Article
  6. Lipids as Targets for Renal Cell Carcinoma Therapy.International journal of molecular sciences · 2023
    Review
  7. Review
  8. A Novel RadioimmuneFrontiers in immunology · 2021
    Article
  9. Endothelial sphingosine 1-phosphate receptors promote vascular normalization and antitumor therapy.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. 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

16 authors at 1 institution in 1 country.

Anthony S FischlEli Lilly and Company, Indianapolis, IN.
Xiaoen WangDepartment of Radiology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Beverly L FalconEli Lilly and Company, Indianapolis, IN.
Rowena Almonte-BaldonadoEli Lilly and Company, Indianapolis, IN.
Diane BodenmillerEli Lilly and Company, Indianapolis, IN.
Glenn EvansEli Lilly and Company, Indianapolis, IN.
Julie StewartEli Lilly and Company, Indianapolis, IN.
Takako WilsonEli Lilly and Company, Indianapolis, IN.
Philip HipskindEli Lilly and Company, Indianapolis, IN.
Jason ManroEli Lilly and Company, Indianapolis, IN.
Mark T UhlikEli Lilly and Company, Indianapolis, IN.
Sudhakar ChintharlapalliEli Lilly and Company, Indianapolis, IN.
Damien GeraldEli Lilly and Company, Indianapolis, IN.
David C AlsopDepartment of Radiology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Laura E BenjaminEli Lilly and Company, Indianapolis, IN.
Rupal S BhattDivision of Hematology and Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts. rbhatt@bidmc.harvard.edu.
Eli Lilly (United States) · US

Funding

Treating the P13-Kinase/AKTP50CA101942 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Wanling Xie · 2003 to 2026
$53.4M
Combating Resistance to Antiangiogenic Therapy in Renal Cell CarcinomaR01CA196996 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BHATT, RUPAL S · 2015 to 2019
$2.0M
NCI NIH HHS P50 CA101942NCI NIH HHS R01 CA196996
6 · The paper itself

Abstract

Inhibition of VEGFR signaling is an effective treatment for renal cell carcinoma, but resistance continues to be a major problem. Recently, the sphingosine phosphate (S1P) signaling pathway has been implicated in tumor growth, angiogenesis, and resistance to antiangiogenic therapy. S1P is a bioactive lipid that serves an essential role in developmental and pathologic angiogenesis via activation of the S1P receptor 1 (S1P1). S1P1 signaling counteracts VEGF signaling and is required for vascular stabilization. We used

Indexed as

Angiogenesis InhibitorsAnimalsAntibodies, MonoclonalCarcinoma, Renal CellCell Line, TumorDrug Therapy, CombinationEndothelial CellsFemaleHumansKidney NeoplasmsLysophospholipidsMaleMiceMice, Inbred C57BLMice, NudeNeovascularization, PathologicAngiogenesis InhibitorsAntibodies, MonoclonalDC101 monoclonal antibodyKdr protein, mouseLysophospholipidsS1pr1 protein, mouseSphingosinesphingosine 1-phosphateSphingosine-1-Phosphate ReceptorsSunitinibVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouseVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID30787172
PMCPMC6992361
OpenAlexW2915626948

What OpenQuestion holds

Textmetadata
LicenceTDM
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.