Evidence map›Paper›PMID 33560598›Full record

ArticleCancer medicine2021

Differential immune signatures in the tumor microenvironment are associated with colon cancer racial disparities.

Thomas Curran, Zequn Sun, Brielle Gerry, Victoria J Findlay, Kristin Wallace, Zihai Li, Chrystal Paulos, Marvella Ford, Mark P Rubinstein, Dongjun Chung and 1 more

Abstract read
In one paragraph

Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. The density of tumour infiltrating lymphocytes in oesophago-gastric cancer varies with disease stage, geographical region and treatment: a post hoc analysis of nine phase III clinical trials.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. A guideline for the statistical analysis of compositional data in immunology.Communications for statistical applications and methods · 2022
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  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

11 authors.

Thomas CurranDepartment of Surgery, Medical University of South Carolina, Charleston, SC, USA.ORCID 0000-0002-9309-4696
Zequn SunDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.
Brielle GerryDepartment of Surgery, Medical University of South Carolina, Charleston, SC, USA.ORCID 0000-0003-0244-7853
Victoria J FindlayDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC, USA.
Kristin WallaceDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.
Zihai LiDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA.
Chrystal PaulosDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA.
Marvella FordDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.
Mark P RubinsteinDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC, USA.
Dongjun ChungThe Pelotonia Institute for Immuno-Oncology, Ohio State University Comprehensive Cancer Center - James, Columbus, OH, USA.ORCID 0000-0002-8072-5671
E Ramsay CampDepartment of Surgery, Baylor College of Medicine, Houston, TX, USA.

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Jian Ouyang · 2009 to 2026
$42.7M
Proteomics CoreP30DK123704 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI DON C. ROCKEY · 2020 to 2026
$8.8M
Project 3: Structural Basis for grp94 Drug Development and Chaperone FunctionP01CA186866 · NCI · OHIO STATE UNIVERSITY · PI GEWIRTH, DANIEL T · 2015 to 2019
$6.7M
South Carolina Cancer Disparities Research Center (SC CaDRe)U54CA210963 · NCI · SOUTH CAROLINA STATE UNIVERSITY · PI SALLEY, JUDITH · 2017 to 2023
$6.1M
Lymphocyte and inflammatory cytokine markers of response in the first-in-human combination of anti-PD-1 mAb and IL-15/IL-15Ra complexes and investigation of mediators of anti-tumor immune responsesR01CA222817 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RUBINSTEIN, MARK P, WRANGLE, JOHN M. · 2019 to 2023
$2.0M
Statistical Models for Genetic Studies, Using Network and Integrative AnalysisR01GM122078 · NIGMS · OHIO STATE UNIVERSITY · PI CHUNG, DONGJUN · 2016 to 2020
$1.9M
Algorithms for Literature-Guided Multi-Platform Identification of Cancer SubtypesR21CA209848 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI CHUNG, DONGJUN, KELEMEN, LINDA E · 2016 to 2017
$358k
NCI NIH HHS P01 CA186866NCI NIH HHS P30 CA138313NCI NIH HHS R01 CA222817NCI NIH HHS R21 CA209848NCI NIH HHS U54 CA210963NIDDK NIH HHS P30 DK123704NIGMS NIH HHS R01 GM122078
6 · The paper itself

Abstract

backgroundDisparities in colon cancer (CC) outcomes may be due to a more aggressive phenotype in African American patients in the setting of a decreased tumor immunity, though the precise mechanism for this result has not been well elucidated. To explore the molecular factors underlying CC disparities, we compared the immunogenomic signatures of CC from African American and European American patients.

methodsWe identified all CC patients from the publicly available Cancer Genome Atlas for whom race and survival data are available. Immunophenotype signatures were established for African American and European American patients. Comparisons were made regarding survival and a multivariable linear regression model was created to determine the association of immune cellular components with race. Differential gene expression was also assessed.

resultsOf the 254 patients identified, 58 (23%) were African American and 196 (77%) were European American. African American patients had a decreased progression free survival (p = 0.04). Tumors from African American patients displayed a reduced fraction of macrophages and CD8

conclusionsDifferences in the tumor immune microenvironment of African American as compared to European American CC specimens may play a role in the survival differences between the groups. These differences may provide targeted therapeutic opportunities.

Indexed as

AgedAge FactorsBlack or African AmericanB-LymphocytesCD8-Positive T-LymphocytesColonic NeoplasmsFemaleGene ExpressionGenes, MHC Class IGenes, MHC Class IIHumansImmunityImmunity, CellularImmunophenotypingLinear ModelsMacrophagescolon cancerimmunogenomicsimmunologyimmunophenotyperacial disparities

Identifiers

PMID33560598
PMCPMC7940243

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.