Evidence map›Paper›PMID 37698493›Full record

ArticleCancer2023

Racial differences in serum chemokines in prostate cancer patients.

Dev Karan, Jo Wick, Seema Dubey, Chandan Kumar-Sinha, Javed Siddiqui, Lakshmi P Kunju, Kenneth A Iczkowski, Arul M Chinnaiyan

Open access · hybridAbstract read
In one paragraph

Article in Cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Dev KaranDepartment of Pathology, MCW Cancer Center and Prostate Cancer Center of Excellence, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.ORCID 0000-0002-0905-0886
Jo WickDepartment of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, Kansas, USA.
Seema DubeyDepartment of Pathology, MCW Cancer Center and Prostate Cancer Center of Excellence, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Chandan Kumar-SinhaMichigan Center for Translational Pathology, Department of Pathology, University of Michigan, Ann Arbor, Michigan, USA.
Javed SiddiquiMichigan Center for Translational Pathology, Department of Pathology, University of Michigan, Ann Arbor, Michigan, USA.
Lakshmi P KunjuMichigan Center for Translational Pathology, Department of Pathology, University of Michigan, Ann Arbor, Michigan, USA.
Kenneth A IczkowskiDepartment of Pathology, MCW Cancer Center and Prostate Cancer Center of Excellence, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Arul M ChinnaiyanMichigan Center for Translational Pathology, Department of Pathology, University of Michigan, Ann Arbor, Michigan, USA.
University of Michigan · USMedical College of Wisconsin · USUniversity of Kansas Medical Center · US

Funding

Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ROY A. JENSEN · 2012 to 2026
$40.1M
Tissue/InformaticsP50CA186786 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Ganesh S Palapattu · 2014 to 2026
$27.6M
Modulation of host intrinsic immunity to reduce prostate cancer disparityR01CA204786 · NCI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI KARAN, DEV · 2016 to 2021
$1.5M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA168524NCI NIH HHS P50 CA186786NCI NIH HHS R01 CA204786
6 · The paper itself

Abstract

backgroundThis study aimed to understand the differential levels of inflammatory chemokines in association with higher prostate cancer incidence and mortality in African American (AA) men than in Caucasians (CA).

methodsThe authors used a chemokine assay to simultaneously measure 40 chemokines and cytokines levels in the serum of preoperative prostate cancer patients and healthy controls of AA and CA races. Selected chemokines (CXCL2, CXCL5, and CCL23) serum level was validated in 211 serum samples from prostate cancer patients and healthy controls. Differential expression of CXCL5 and CCL23 was analyzed using immunohistochemistry in a representative cohort of prostate tumor tissues of AA and CA races.

resultsRace-specific comparisons from 211 serum samples showed significantly higher levels of CXCL2 (control: 3104.0 pg/mL vs. cancer: 2451.0 pg/mL) and CXCL5 (control: 5189.0 pg/mL vs. cancer: 5459.0 pg/mL) in AA men than in CAs (CXCL2; control: 1155.0 pg/mL vs. cancer: 889.3 pg/mL, and CXCL5; control: 1183.0 pg/mL vs. cancer: 977.5 pg/mL). CCL23 differed significantly within and between the races with a lower level in AA cancer cases (454.5 vs. 966.6 pg/mL) than healthy controls (740.5 vs. 1263.0 pg/mL). Patient age, prostate-specific antigen, or Gleason scores were not significantly associated with these chemokines. Immunostaining for CXCL5 and CCL23 in a representative cohort of archival prostate tissues displayed significantly higher CXCL5 in prostate tumors than in adjacent benign tissues, whereas CCL23 was nondetectable in most of the analyzed tumor tissues.

conclusionLower levels of CCL23 in AA prostate cancer patient sera and tumor tissues and high CXCL2 and CXCL5 may contribute to aggressive prostate cancer, as often seen in AA men. The disproportionate levels of serum chemokines associated with race warrant further exploration to improve equitability in precision oncology to benefit prostate cancer patients.

Indexed as

Precision MedicineProstatic NeoplasmsChemokinesHumansMaleProstate-Specific AntigenRace FactorsChemokinesProstate-Specific AntigenCCL23chemokines profileCXCL2CXCL5prostate cancerracial disparity

Identifiers

PMID37698493
PMCPMC12415822
OpenAlexW4386623850

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.