Evidence map›Paper›PMID 28764974›Full record

ArticleCytokine2017

Associations between genetic and epigenetic variations in cytokine genes and mild persistent breast pain in women following breast cancer surgery.

Kimberly E Stephens, Jon D Levine, Bradley E Aouizerat, Steven M Paul, Gary Abrams, Yvette P Conley, Christine Miaskowski

Open access · greenAbstract read
In one paragraph

Article in Cytokine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 4 pooled it
3.8field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 4 syntheses or guidelines pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Systematic review of genetic polymorphisms associated with psychoneurological symptoms in breast cancer survivors.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2019
    Pooled it
  4. Pooled it
  5. Article
  6. Review
  7. Epigenetic Landscapes of Pain: DNA Methylation Dynamics in Chronic Pain.International journal of molecular sciences · 2024
    Review
  8. Article
  9. Neurotrophin-3 (NT-3) as a Potential Biomarker of the Peripheral Nervous System Damage Following Breast Cancer Treatment.Pathophysiology : the official journal of the International Society for Pathophysiology · 2023
    Article
  10. Pain associated with breast cancer: etiologies and therapies.Frontiers in pain research (Lausanne, Switzerland) · 2023
    Review
  11. Review
  12. Article
  13. Review
  14. Genetic Variants of thePharmacogenomics and personalized medicine · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Observational
  20. Review
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

7 authors at 4 institutions in 1 country.

Kimberly E StephensSchool of Medicine, Johns Hopkins University, Baltimore, MD, United States.
Jon D LevineSchool of Medicine, University of California, San Francisco, CA, United States.
Bradley E AouizeratCollege of Dentistry, New York University, New York, NY, United States.
Steven M PaulSchool of Nursing, University of California, San Francisco, CA, United States.
Gary AbramsSchool of Medicine, University of California, San Francisco, CA, United States.
Yvette P ConleySchool of Nursing, University of Pittsburgh, Pittsburgh, PA, United States.
Christine MiaskowskiSchool of Nursing, University of California, San Francisco, CA, United States. Electronic address: chris.miaskowski@ucsf.edu.
University of California, San Francisco · USJohns Hopkins Medicine · USNew York University · USUniversity of Pittsburgh · US

Funding

UCSF CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR024131 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JOHNSTON, S. CLAIBORNE · 2006 to 2011
$111.2M
NURSING RESEARCH TRAINING IN SYMPTOM MANAGEMENTT32NR007088 · NINR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LEE, KATHRYN · 1996 to 2015
$7.5M
Symptom Management After Breast Cancer SurgeryR01CA107091 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MIASKOWSKI, CHRISTINE A. · 2003 to 2008
$4.5M
Long-term Arm Morbidity Following Breast Cancer TreatmentR01CA118658 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MIASKOWSKI, CHRISTINE A. · 2006 to 2010
$3.5M
Advancing the Science of Symptom Management in Oncology PatientsK05CA168960 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MIASKOWSKI, CHRISTINE A. · 2013 to 2017
$453k
Genome-wide profiling of histone modifications associated with persistent painF32NR015728 · NINR · JOHNS HOPKINS UNIVERSITY · PI STEPHENS, KIMBERLY E · 2016 to 2017
$57k
NCI NIH HHS K05 CA168960NCI NIH HHS R01 CA107091NCI NIH HHS R01 CA118658NCRR NIH HHS UL1 RR024131NINR NIH HHS F32 NR015728NINR NIH HHS T32 NR007088
6 · The paper itself

Abstract

Persistent pain following breast cancer surgery is a significant problem. Both inherited and acquired mechanisms of inflammation appear to play a role in the development and maintenance of persistent pain. In this longitudinal study, growth mixture modeling was used to identify persistent breast pain phenotypes based on pain assessments obtained prior to and monthly for 6months following breast cancer surgery. Associations between the "no pain" and "mild pain" phenotypes and single nucleotide polymorphisms (SNPs) spanning 15 cytokine genes were evaluated. The methylation status of the CpG sites found in the promoters of genes associated with pain group membership was determined using bisulfite sequencing. In the multivariate analysis, three SNPs (i.e., interleukin 6 (IL6) rs2069840, C-X-C motif chemokine ligand 8 (CXCL8) rs4073, tumor necrosis factor (TNF) rs1800610) and two TNF CpG sites (i.e., c.-350C, c.-344C) were associated with pain group membership. These findings suggest that variations in IL6, CXCL8, and TNF are associated with the development and maintenance of mild persistent breast pain. CpG methylation within the TNF promoter may provide an additional mechanism through which TNF alters the risk for mild persistent breast pain after breast cancer surgery. These genetic and epigenetic variations may help to identify individuals who are predisposed to the development of mild levels of persistent breast pain following breast cancer surgery.

Indexed as

Epigenesis, GeneticGenetic Association StudiesBreast NeoplasmsDemographyDNA MethylationFemaleHumansInterleukin-6Interleukin-8Logistic ModelsMastodyniaMiddle AgedPolymorphism, Single NucleotidePromoter Regions, GeneticTumor Necrosis Factor-alphaCXCL8 protein, humanInterleukin-6Interleukin-8Tumor Necrosis Factor-alphaBreast cancerC-X-C motif chemokine ligand 8Cytokine genesDNA methylationEpigeneticsInterleukin 6Persistent painPost-mastectomy painPost-surgical painTumor necrosis factor

Identifiers

PMID28764974
PMCPMC5675785
OpenAlexW2740034899

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.