Evidence map›Paper›PMID 32114681›Full record

ArticleCancer immunology, immunotherapy : CII2020

Neutrophils are mediators of metastatic prostate cancer progression in bone.

Diane L Costanzo-Garvey, Tyler Keeley, Adam J Case, Gabrielle F Watson, Massar Alsamraae, Yangsheng Yu, Kaihong Su, Cortney E Heim, Tammy Kielian, Colm Morrissey and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
3.4field-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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Tumor-associated neutrophils suppress CD8British journal of cancer · 2024
    Pooled it
  2. Trial
  3. Review
  4. Human Group IIA Secreted Phospholipase AInternational journal of molecular sciences · 2026
    Review
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  7. Article
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  9. Article
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  12. Article
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  16. Article
  17. Immune mediated support of metastasis: Implication for bone invasion.Cancer communications (London, England) · 2024
    Review
  18. Article
  19. Article
  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

12 authors at 5 institutions in 1 country.

Diane L Costanzo-GarveyDepartment of Pathology and Microbiology, University of Nebraska Medical Center, 985900 Nebraska Med Center, Omaha, NE, 68192, USA.
Tyler KeeleyDepartment of Pathology and Microbiology, University of Nebraska Medical Center, 985900 Nebraska Med Center, Omaha, NE, 68192, USA.
Adam J CaseDepartment of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, NE, USA.
Gabrielle F WatsonDepartment of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, NE, USA.
Massar AlsamraaeDepartment of Pathology and Microbiology, University of Nebraska Medical Center, 985900 Nebraska Med Center, Omaha, NE, 68192, USA.
Yangsheng YuDepartment of Pathology and Microbiology, University of Nebraska Medical Center, 985900 Nebraska Med Center, Omaha, NE, 68192, USA.
Kaihong SuDepartment of Pathology and Microbiology, University of Nebraska Medical Center, 985900 Nebraska Med Center, Omaha, NE, 68192, USA.
Cortney E HeimDepartment of Pathology and Microbiology, University of Nebraska Medical Center, 985900 Nebraska Med Center, Omaha, NE, 68192, USA.
Tammy KielianDepartment of Pathology and Microbiology, University of Nebraska Medical Center, 985900 Nebraska Med Center, Omaha, NE, 68192, USA.
Colm MorrisseyDepartment of Urology, University of Washington, Seattle, WA, USA.
Jeremy S FrielingTumor Biology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Leah M CookDepartment of Pathology and Microbiology, University of Nebraska Medical Center, 985900 Nebraska Med Center, Omaha, NE, 68192, USA. leah.cook@unmc.edu.ORCID http://orcid.org/0000-0002-9996-7419
University of Nebraska Medical Center · USCalifornia State University, San Bernardino · USMoffitt Cancer Center · USNebraska Medical Center · USUniversity of Washington · US

Funding

TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI John Kyung Lee · 2002 to 2026
$58.1M
The S. aureus biofilm lifecycleP01AI083211 · NIAID · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAYLES, KENNETH W. · 2009 to 2023
$32.1M
Redox Regulation of T-lymphocytes in Sympathoexcitation-associated HypertensionR00HL123471 · NHLBI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI CASE, ADAM J · 2016 to 2018
$765k
NCI NIH HHS P50 CA097186NCI NIH HHS P50CA97186NHLBI NIH HHS R00 HL123471NIAID NIH HHS P01 AI083211NIH HHS R00HL123471
6 · The paper itself

Abstract

Bone metastatic prostate cancer (BM-PCa) significantly reduces overall patient survival and is currently incurable. Current standard immunotherapy showed promising results for PCa patients with metastatic, but less advanced, disease (i.e., fewer than 20 bone lesions) suggesting that PCa growth in bone contributes to response to immunotherapy. We found that: (1) PCa stimulates recruitment of neutrophils, the most abundant immune cell in bone, and (2) that neutrophils heavily infiltrate regions of prostate tumor in bone of BM-PCa patients. Based on these findings, we examined the impact of direct neutrophil-prostate cancer interactions on prostate cancer growth. Bone marrow neutrophils directly induced apoptosis of PCa in vitro and in vivo, such that neutrophil depletion in bone metastasis models enhanced BM-PCa growth. Neutrophil-mediated PCa killing was found to be mediated by suppression of STAT5, a transcription factor shown to promote PCa progression. However, as the tumor progressed in bone over time, neutrophils from late-stage bone tumors failed to elicit cytotoxic effector responses to PCa. These findings are the first to demonstrate that bone-resident neutrophils inhibit PCa and that BM-PCa are able to progress via evasion of neutrophil-mediated killing. Enhancing neutrophil cytotoxicity in bone may present a novel therapeutic option for bone metastatic prostate cancer.

Indexed as

AnimalsBone NeoplasmsCell Line, TumorDisease Models, AnimalDisease ProgressionHumansMaleMiceNeutrophilsProstatic NeoplasmsBoneCancerMetastasisNeutrophilsProstateSTAT5

Identifiers

PMID32114681
PMCPMC7230043
OpenAlexW3008472710

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.