Evidence map›Paper›PMID 37270599›Full record

ArticleMolecular cancer2023

CXCR2 expression during melanoma tumorigenesis controls transcriptional programs that facilitate tumor growth.

J Yang, K Bergdorf, C Yan, W Luo, S C Chen, G D Ayers, Q Liu, X Liu, M Boothby, V L Weiss and 7 more

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Interleukin-8 in health and disease.Molecular biomedicine · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Tfcp2l1 as a central integrator of hypoxia, dedifferentiation, and tumor progression.Journal of experimental & clinical cancer research : CR · 2025
    Review
  9. Article
  10. Article
  11. Review
  12. PTEN: a new dawn in Parkinson's disease treatment.Frontiers in cellular neuroscience · 2025
    Review
  13. Article
  14. Harnessing the potential of CD40 agonism in cancer therapy.Cytokine & growth factor reviews · 2024
    Review
  15. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 2 countries.

J Yang *TVHS Department of Veterans Affairs, Nashville, TN, 37212, USA.
K Bergdorf *TVHS Department of Veterans Affairs, Nashville, TN, 37212, USA.
C Yan *TVHS Department of Veterans Affairs, Nashville, TN, 37212, USA.
W LuoTVHS Department of Veterans Affairs, Nashville, TN, 37212, USA.
S C ChenDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, 37203-1742, USA.
G D AyersDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, 37203-1742, USA.
Q LiuDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, 37203-1742, USA.
X LiuDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, 37203-1742, USA.
M BoothbyDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
V L WeissDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
S M GrovesDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
A N OleskieDepartment of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN, 37240, USA.
X ZhangDepartment of Genomic Medicine, MD Anderson Cancer Center, University of Texas, Houston, TX, 77030, USA.
D Y MaedaSyntrix Pharmaceuticals, Auburn, WA, 98001, USA.
J A ZebalaSyntrix Pharmaceuticals, Auburn, WA, 98001, USA.
V QuarantaDepartment of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN, 37240, USA.
A RichmondTVHS Department of Veterans Affairs, Nashville, TN, 37212, USA. ann.richmond@vanderbilt.edu.
Vanderbilt University · USVanderbilt University Medical Center · USSyntrix Biosystems (United States) · USThe University of Texas MD Anderson Cancer Center · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ben Ho Park · 1995 to 2026
$172.8M
Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Shondra Michelle Miller · 1985 to 2026
$166.9M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MARY Kay WASHINGTON · 2002 to 2026
$29.9M
MULTIDISCIPLINARY BASIC RESEARCH TRAINING IN CANCERT32CA009592 · NCI · VANDERBILT UNIVERSITY · PI Justin M Balko, Julie A Rhoades (Sterling) · 1987 to 2026
$10.4M
BIOCHEMICAL &CHEMICAL TRAINING FOR CANCER RESEARCHT32CA009582 · NCI · VANDERBILT UNIVERSITY · PI David K Cortez · 1987 to 2026
$8.8M
Single-Cell Biology and Data Analysis Shared Resource (SCB-DA SR)U54CA217450 · NCI · VANDERBILT UNIVERSITY · PI WEAVER, ALISSA M · 2018 to 2022
$8.5M
Integrated Biological Systems Training in OncologyT32CA119925 · NCI · VANDERBILT UNIVERSITY · PI Vivian Gama, William Patrick Tansey · 2008 to 2026
$7.6M
Targeting the NF-kappaB Pathway in MelanomaR01CA116021 · NCI · VANDERBILT UNIVERSITY · PI RICHMOND, ANN, YAN, CHI · 2005 to 2024
$6.7M
The Role of Cancer-Associated Fibroblasts in Thyroid CarcinomaR01CA272875 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WEISS, VIVIAN LEE · 2022 to 2025
$2.5M
The role of Wnt signaling in aggressive thyroid carcinomaK08CA240901 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WEISS, VIVIAN LEE · 2020 to 2024
$1.1M
Pannoramic 250 BF Flash Tissue Microarray systemS10OD016355 · OD · VANDERBILT UNIVERSITY · PI BOYD, KELLI L. · 2014 to 2014
$453k
Regulation of Primary Human Beta Cell Culture by E2A1-14R21CA116022 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI CHOI, JOHN K · 2005 to 2006
$282k
BLRD VA I01 BX002301BLRD VA IK6 BX005225NCI NIH HHS K08 CA240901NCI NIH HHS P30 CA021765NCI NIH HHS P30 CA068485NCI NIH HHS R01 CA116021NCI NIH HHS R01 CA272875NCI NIH HHS R21 CA116022NCI NIH HHS T32 CA009582NCI NIH HHS T32 CA009592NCI NIH HHS T32 CA119925NCI NIH HHS U54 CA217450NIDDK NIH HHS P30 DK058404NIH HHS S10 OD016355NIH HHS S10 OD023475
6 · The paper itself

Abstract

backgroundThough the CXCR2 chemokine receptor is known to play a key role in cancer growth and response to therapy, a direct link between expression of CXCR2 in tumor progenitor cells during induction of tumorigenesis has not been established.

methodsTo characterize the role of CXCR2 during melanoma tumorigenesis, we generated tamoxifen-inducible tyrosinase-promoter driven Braf

resultsGenetic loss of Cxcr2 or pharmacological inhibition of CXCR1/CXCR2 during melanoma tumor induction resulted in key changes in gene expression that reduced tumor incidence/growth and increased anti-tumor immunity. Interestingly, after Cxcr2 ablation, Tfcp2l1, a key tumor suppressive transcription factor, was the only gene significantly induced with a log

conclusionsHere, we provide novel mechanistic insight revealing how loss of Cxcr2 expression/activity in melanoma tumor progenitor cells results in reduced tumor burden and creation of an anti-tumor immune microenvironment. This mechanism entails an increase in expression of the tumor suppressive transcription factor, Tfcp2l1, along with alteration in the expression of genes involved in growth regulation, tumor suppression, stemness, differentiation, and immune modulation. These gene expression changes are coincident with reduction in the activation of key growth regulatory pathways, including AKT and mTOR.

Indexed as

MelanomaProto-Oncogene Proteins B-rafReceptors, Interleukin-8BAnimalsCarcinogenesisCell Line, TumorCell Transformation, NeoplasticMiceTumor MicroenvironmentCxcr2 protein, mouseProto-Oncogene Proteins B-rafReceptors, Interleukin-8BCXCR2Genetic mouse modelsGenomic analysisMelanomaTumor immune microenvironment

Identifiers

PMID37270599
PMCPMC10239119
OpenAlexW4379259427

What OpenQuestion holds

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Registered trials

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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.