Evidence map›Paper›PMID 25434743›Full record

ReviewAdvances in biological regulation2015

Sphingolipids in the DNA damage response.

Brittany Carroll, Jane Catalina Donaldson, Lina Obeid

Open access · greenAbstract readReview
In one paragraph

Review in Advances in biological regulation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. SMPDL3b modulates radiation-induced DNA damage response in renal podocytes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  4. Review
  5. Article
  6. Review
  7. Multi-Omics Integration Highlights the Role of Ubiquitination in CClInternational journal of molecular sciences · 2020
    Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Metabolomics study of the therapeutic mechanism ofClinical interventions in aging · 2018
    Article
  18. Ceramide Signaling and p53 Pathways.Advances in cancer research · 2018
    Review
  19. Article
  20. 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

3 authors at 2 institutions in 1 country.

Brittany CarrollDepartment of Medicine, Stony Brook University, Stony Brook, NY 11794, USA; Stony Brook Cancer Center, Stony Brook University, Stony Brook, NY 11794, USA.
Jane Catalina DonaldsonDepartment of Medicine, Stony Brook University, Stony Brook, NY 11794, USA; Stony Brook Cancer Center, Stony Brook University, Stony Brook, NY 11794, USA.
Lina ObeidNorthport VA Medical Center, Northport, NY 11768, USA; Department of Medicine, Stony Brook University, Stony Brook, NY 11794, USA; Stony Brook Cancer Center, Stony Brook University, Stony Brook, NY 11794, USA. Electronic address: Lina.Obeid@stonybrookmedicine.edu.
Stony Brook University · USNorthport VA Medical Center · US

Funding

Sphingolipids in Cancer Therapy and AngiogenesisP01CA097132 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI Daniel Canals · 2003 to 2026
$30.8M
Role and Regulation of Ceramide Synthases in ApoptosisR01GM097741 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI LUBERTO, CHIARA · 2011 to 2019
$3.5M
Sphingosine Phosphate Role in InflammationR01GM062887 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI OBEID, LINA M · 2001 to 2009
$2.1M
Regulation of Sphingosine Kinase 1 by p53 and Caspase 2F31CA186547 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI CARROLL, BRITTANY L · 2014 to 2014
$30k
Regulation and Role of Ceramidase in InflammationI01BX000156 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI OBEID, LINA M · 2009 to 2017
–
BLRD VA I01 BX000156NCI NIH HHS F31 CA186547NCI NIH HHS F31 CA186547-01NCI NIH HHS P01 CA097132NIGMS NIH HHS GM062887NIGMS NIH HHS R01 GM062887NIGMS NIH HHS R01 GM097741
6 · The paper itself

Abstract

Recently, sphingolipid metabolizing enzymes have emerged as important targets of many chemotherapeutics and DNA damaging agents and therefore play significant roles in mediating the physiological response of the cell to DNA damage. In this review we will highlight points of connection between the DNA damage response (DDR) and sphingolipid metabolism; specifically how certain sphingolipid enzymes are regulated in response to DNA damage and how the bioactive lipids produced by these enzymes affect cell fate.

Indexed as

DNA RepairAnimalsApoptosisApoptosis Regulatory ProteinsAtaxia Telangiectasia Mutated ProteinsCell Cycle CheckpointsDNADNA DamageGene Expression RegulationHumansLipid MetabolismLysophospholipidsSignal TransductionSphingosineTumor Suppressor Protein p53Apoptosis Regulatory ProteinsAtaxia Telangiectasia Mutated ProteinsATM protein, humanATR protein, humanDNALysophospholipidsSphingosinesphingosine 1-phosphateTumor Suppressor Protein p53CeramideDNA damageSphingosineSphingosine 1-phosphate

Identifiers

PMID25434743
PMCPMC4425997
OpenAlexW2080794658

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.