Evidence map›Paper›PMID 35440548›Full record

ArticleNature communications2022

TNF is a potential therapeutic target to suppress prostatic inflammation and hyperplasia in autoimmune disease.

Renee E Vickman, LaTayia Aaron-Brooks, Renyuan Zhang, Nadia A Lanman, Brittany Lapin, Victoria Gil, Max Greenberg, Takeshi Sasaki, Gregory M Cresswell, Meaghan M Broman and 11 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06062875 (Effects of TNF Blockade on Human BPH/LUTS), which is not on this map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
16.7field-weighted citation impact, top 1% 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.

NCT06062875 phase2recruitingnot on this mapstarted 2024, after this paper: background citation

Effects of TNF Blockade on Human BPH/LUTS

TypeinterventionalSponsorEndeavor HealthRan2024 to 2028Enrolled70ConditionsBenign Prostatic Hyperplasia (BPH)ArmsAdalimumab
3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Immune dysregulation in the prostates of C57BL/6The Journal of pathology · 2026
    Article
  3. Article
  4. Article
  5. High-Throughput Proteomic and Glycoproteomic Analyses in Benign Prostatic Hyperplasia.Journal of the American Society for Mass Spectrometry · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
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  14. Article
  15. Article
  16. Article
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  18. Article
  19. The Combination ofThe world journal of men's health · 2025
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 5 institutions in 2 countries.

Renee E VickmanDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA.ORCID 0000-0002-5614-9221
LaTayia Aaron-BrooksDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA.
Renyuan ZhangDepartment of Cancer Genetics and Genomics, Roswell Park Comprehensive Cancer Center, Buffalo, NY, 14263, USA.ORCID 0000-0003-1435-5075
Nadia A LanmanDepartment of Comparative Pathobiology, Purdue University, West Lafayette, IN, 47907, USA.ORCID 0000-0002-1819-7070
Brittany LapinBiostatistics and Research Informatics, NorthShore University HealthSystem, Evanston, IL, 60201, USA.ORCID 0000-0002-4314-2282
Victoria GilDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA.ORCID 0000-0002-2569-4163
Max GreenbergDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA.
Takeshi SasakiDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA.
Gregory M CresswellDepartment of Comparative Pathobiology, Purdue University, West Lafayette, IN, 47907, USA.
Meaghan M BromanDepartment of Comparative Pathobiology, Purdue University, West Lafayette, IN, 47907, USA.
J Sebastian PaezPurdue Center for Cancer Research, Purdue University, West Lafayette, IN, 47907, USA.ORCID 0000-0002-0065-1474
Jacqueline PetkewiczDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA.
Pooja TalatyDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA.
Brian T HelfandDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA.
Alexander P GlaserDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA.ORCID 0000-0003-1781-9023
Chi-Hsiung WangDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA.
Omar E FrancoDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA.
Timothy L RatliffDepartment of Comparative Pathobiology, Purdue University, West Lafayette, IN, 47907, USA.ORCID 0000-0003-4221-5416
Kent L NastiukDepartment of Cancer Genetics and Genomics, Roswell Park Comprehensive Cancer Center, Buffalo, NY, 14263, USA.
Susan E CrawfordDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA.
Simon W HaywardDepartment of Surgery, NorthShore University HealthSystem, an Academic Affiliate of the University of Chicago Pritzker School of Medicine, Evanston, IL, 60201, USA. shayward@northshore.org.ORCID 0000-0002-6059-6550
NorthShore University HealthSystem · USPurdue University West Lafayette · USRoswell Park Comprehensive Cancer Center · USGeorge Washington University · USMeharry Medical College · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI Dean G. Tang · 1985 to 2026
$116.6M
Tumor Microenvironment and Metastasis ProgramP30CA082709 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Sara K Quinney · 1999 to 2026
$59.3M
Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI Andrea L Kasinski · 1985 to 2026
$43.4M
Inflammatory Pathways in BPH/LUTSR01DK117906 · NIDDK · ENDEAVOR HEALTH CLINICAL OPERATIONS · PI HAYWARD, SIMON W, THUMBIKAT, PRAVEEN · 2018 to 2021
$2.2M
Leukocytic Phenotypes Associated with BPH ProgressionP20DK116185 · NIDDK · ENDEAVOR HEALTH CLINICAL OPERATIONS · PI RATLIFF, TIMOTHY L. · 2018 to 2019
$629k
Photoacoustic Micro-Imaging system for Shared Tumor Imaging Resource at Roswell PS10OD010393 · OD · ROSWELL PARK CANCER INSTITUTE CORP · PI SESHADRI, MUKUND · 2012 to 2012
$596k
NCI NIH HHS P30 CA016056NCI NIH HHS P30 CA023168NCI NIH HHS P30 CA082709NIDDK NIH HHS P20 DK116185NIDDK NIH HHS R01 DK117906NIH HHS S10 OD010393
6 · The paper itself

Abstract

Autoimmune (AI) diseases can affect many organs; however, the prostate has not been considered to be a primary target of these systemic inflammatory processes. Here, we utilize medical record data, patient samples, and in vivo models to evaluate the impact of inflammation, as seen in AI diseases, on prostate tissue. Human and mouse tissues are used to examine whether systemic targeting of inflammation limits prostatic inflammation and hyperplasia. Evaluation of 112,152 medical records indicates that benign prostatic hyperplasia (BPH) prevalence is significantly higher among patients with AI diseases. Furthermore, treating these patients with tumor necrosis factor (TNF)-antagonists significantly decreases BPH incidence. Single-cell RNA-seq and in vitro assays suggest that macrophage-derived TNF stimulates BPH-derived fibroblast proliferation. TNF blockade significantly reduces epithelial hyperplasia, NFκB activation, and macrophage-mediated inflammation within prostate tissues. Together, these studies show that patients with AI diseases have a heightened susceptibility to BPH and that reducing inflammation with a therapeutic agent can suppress BPH.

Indexed as

Autoimmune DiseasesProstatic HyperplasiaProstatitisAnimalsCell LineHumansHyperplasiaInflammationMaleMice

Identifiers

PMID35440548
PMCPMC9018703
OpenAlexW4224278902

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.