Evidence map›Paper›PMID 33022812›Full record

ArticleThe Prostate2021

Neuropeptide Y nerve paracrine regulation of prostate cancer oncogenesis and therapy resistance.

Yi Ding, MinJae Lee, Yan Gao, Ping Bu, Christian Coarfa, Brian Miles, Arun Sreekumar, Chad J Creighton, Gustavo Ayala

Open access · hybridAbstract read
In one paragraph

Article in The Prostate, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Neuroscience in prostate cancer.Prostate cancer and prostatic diseases · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. TargetingPharmaceuticals (Basel, Switzerland) · 2026
    Article
  8. Article
  9. Review
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  11. Review
  12. Article
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  14. Article
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  17. Integration Analysis of Single-Cell Multi-Omics Reveals Prostate Cancer Heterogeneity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  18. Article
  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

9 authors at 3 institutions in 1 country.

Yi DingDepartment of Pathology and Laboratory Medicine, McGovern School of Medicine, University of Texas Health Sciences Center Medical School, Houston, Texas, USA.
MinJae LeeBiostatistics, Epidemiology, and Research Design (BERD) Core, Department of Internal Medicine, University of Texas Health Sciences Center Medical School, Houston, Texas, USA.
Yan GaoDepartment of Pathology and Laboratory Medicine, McGovern School of Medicine, University of Texas Health Sciences Center Medical School, Houston, Texas, USA.
Ping BuDepartment of Pathology and Laboratory Medicine, McGovern School of Medicine, University of Texas Health Sciences Center Medical School, Houston, Texas, USA.
Christian CoarfaDepartment of Molecular & Cell Biology, Baylor College of Medicine, Houston, Texas, USA.
Brian MilesDepartment of Urology, The Methodist Hospital, Houston, Texas, USA.
Arun SreekumarDepartment of Pathology and Laboratory Medicine, McGovern School of Medicine, University of Texas Health Sciences Center Medical School, Houston, Texas, USA.
Chad J CreightonDepartment of Internal Medicine, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas, USA.
Gustavo AyalaBiostatistics, Epidemiology, and Research Design (BERD) Core, Department of Internal Medicine, University of Texas Health Sciences Center Medical School, Houston, Texas, USA.ORCID 0000-0002-5288-0244
The University of Texas Health Science Center at Houston · USBaylor College of Medicine · USMethodist Hospital · US

Funding

Convalescent Plasma to Limit Coronavirus Associated ComplicationsUL1TR003167 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KARP, DANIEL D, MCPHERSON, DAVID D · 2019 to 2023
$45.3M
UT Southwestern Center for Translational MedicineUL1TR003163 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI TOTO, ROBERT DANIEL · 2021 to 2025
$39.3M
Neurogenesis in the Prostate Cancer MicroenvironmentU54CA126568 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ITTMANN, MICHAEL M · 2006 to 2010
$3.0M
METABOLOMIC PROFILING AND BIOLOGIC BASIS OF RACIAL DISPARITY IN PROSTATE CANCERU01CA167234 · NCI · BAYLOR COLLEGE OF MEDICINE · PI PALAPATTU, GANESH S, SREEKUMAR, ARUN · 2012 to 2016
$1.9M
Integrative Metabolomics of Prostate Cancer ProgressionR01CA133458 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SREEKUMAR, ARUN · 2008 to 2012
$1.6M
Comprehensive Tumor Microenvironment Based Prediction Models in Prostate CancerR01CA140734 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI AYALA, GUSTAVO ENRIQUE · 2011 to 2015
$1.5M
NCATS NIH HHS UL1 TR003163NCATS NIH HHS UL1 TR003167NCI NIH HHS R01 CA133458NCI NIH HHS R01 CA140734NCI NIH HHS RO1CA133458NCI NIH HHS RO1 CA140734-03NCI NIH HHS TMEN U54CA126568-01NCI NIH HHS U01 CA167234NCI NIH HHS U54 CA126568
6 · The paper itself

Abstract

backgroundNerves are key factors in prostate cancer (PCa) progression. Here, we propose that neuropeptide Y (NPY) nerves are key regulators of cancer-nerve interaction.

methodsWe used in vitro models for NPY inhibition studies and subsequent metabolomics, apoptotic and migration assays, and nuclear transcription factor-κB (NF-κB) translocation studies. Human naïve and radiated PCa tissues were used for NPY nerve density biomarker studies. Tissues derived from a Botox denervation clinical trial were used to corroborate metabolomic changes in humans.

resultsCancer cells increase NPY positive nerves in vitro and in preneoplastic human tissues. NPY-specific inhibition resulted in increased cancer apoptosis, decreased motility, and energetic metabolic pathway changes. A comparison of metabolomic response in NPY-inhibited cells with the transcriptome response in human PCa patients treated with Botox showed shared 13 pathways, including the tricarboxylic acid cycle. We identified that NF-κB is a potential NPY downstream mediator. Using in vitro models and tissues derived from a previous human chemical denervation study, we show that Botox specifically, but not exclusively, inhibits NPY in cancer. Quantification of NPY nerves is independently predictive of PCa-specific death. Finally, NPY nerves might be involved in radiation therapy (RT) resistance, as radiation-induced apoptosis is reduced when PCa cells are cocultured with dorsal root ganglia/nerves and NPY positive nerves are increased in prostates of patients that failed RT.

conclusionThese data suggest that targeting the NPY neural microenvironment may represent a therapeutic approach for the treatment of PCa and resistance through the regulation of multiple oncogenic mechanisms.

Indexed as

AdolescentAdultAge FactorsAnimalsApoptosisAxonsBotulinum Toxins, Type ACarcinogenesisCell Line, TumorChildHumansMaleMetabolomeMiceMiddle AgedNervous SystemBotulinum Toxins, Type ANeuropeptide YNF-kappa Bcancermetabolismnervesneurogenesisneuropeptide Yprostateradiation resistance

Identifiers

PMID33022812
PMCPMC7756863
OpenAlexW3091906690

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.