Evidence map›Paper›PMID 26174474›Full record

ArticleThe Prostate2015

Characterization of autoimmune inflammation induced prostate stem cell expansion.

Hsing-Hui Wang, Liang Wang, Travis J Jerde, Bin-Da Chan, Cagri A Savran, Grant N Burcham, Scott Crist, Timothy L Ratliff

Open access · hybridAbstract read
In one paragraph

Article in The Prostate, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Immune dysregulation in the prostates of C57BL/6The Journal of pathology · 2026
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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

8 authors at 3 institutions in 2 countries.

Hsing-Hui WangDepartment of Comparative Pathobiology, Purdue University, West Lafayette, Indiana.
Liang WangDepartment of Pharmacology and Toxicology and Department of Urology, Indiana University, Indianapolis, Indiana.
Travis J JerdeDepartment of Pharmacology and Toxicology and Department of Urology, Indiana University, Indianapolis, Indiana.
Bin-Da ChanSchool of Mechanical Engineering, Purdue University, West Lafayette, Indiana.
Cagri A SavranSchool of Mechanical Engineering, Purdue University, West Lafayette, Indiana.
Grant N BurchamDepartment of Comparative Pathobiology, Purdue University, West Lafayette, Indiana.
Scott CristDepartment of Comparative Pathobiology, Purdue University, West Lafayette, Indiana.
Timothy L RatliffDepartment of Comparative Pathobiology, Purdue University, West Lafayette, Indiana.
Purdue University West Lafayette · USCenter for Cancer Research · USIndiana University – Purdue University Indianapolis · US

Funding

Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI Majid Kazemian · 1985 to 2026
$43.4M
Initiation and Regulation of Chronic Autoimmune Prostate InflammationR01DK084454 · NIDDK · PURDUE UNIVERSITY · PI RATLIFF, TIMOTHY L. · 2009 to 2015
$2.0M
IGF-mediated survival and proliferation in inflamed prostateK01DK092366 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI JERDE, TRAVIS J · 2012 to 2016
$597k
Use of Micro-RNA Arrays to Identify MDSC Functional Pathways and MarkersR21CA173918 · NCI · PURDUE UNIVERSITY · PI RATLIFF, TIMOTHY L. · 2013 to 2014
$369k
NCI NIH HHS P30 CA023168NCI NIH HHS R21 CA173918NIDDK NIH HHS 2R01DK084454-05NIDDK NIH HHS K01 DK092366NIDDK NIH HHS R01 DK084454
6 · The paper itself

Abstract

backgroundThe presence of inflammation in prostate cancer (PCa) and benign prostate hyperplasia (BPH) has been well described but the cellular mechanisms by which inflammation modulates the prostate are currently unclear. Prostate stem cells (PSC) not only maintain prostate homeostasis but also are considered to be the cell of origin of PCa and an important contributor to BPH. However, the impact of inflammation on PSC is not well understood. Therefore, we initiated studies to evaluate the effect of inflammation on PSC.

methodOvalbumin specific CD8(+) T cells were intravenously delivered to intact and castrated prostate ovalbumin expressing transgenic-3 (POET-3) mice to induce inflammation. Lin (CD45/CD31)(-) Sca1(+) CD49f(+) cells (LSC) and progenitor cells within LSC were determined by flow cytometry. Sorted LSC were subjected to a prostate sphere forming assay to evaluate PSC clonal propagation, proliferation, immediate differentiation, and self-renewal ability. Density of individual spheres was measured by a cantilever-based resonator weighing system. Morphology and characterization of prostate spheres was determined by hematoxylin and eosin (H&E) staining and immunohistochemistry (IHC). Finally, immediate PSC differentiation in sphere formation was determined by immunofluorescence for epithelial cytokeratin markers cytokeratin (CK) 5 and CK8.

resultData presented here demonstrate a significant expansion of the proliferative (BrdU(+) ) LSC population, including CK5(+) , p63(+) , CK18(+) cells, as well as intermediate cells (CK5(+) /CK8(+) ) in inflamed prostates. Histological images reveal that PSC from inflamed prostates produce significantly larger spheres, indicating that the enhanced proliferation observed in LSC is sustained in vitro in the absence of inflammatory mediators. In addition, cultures from inflamed PSC yielded increased number of tubule-like spheres. These tube-like spheres grown from PSCs isolated from inflamed mice exhibited stratification of a CK8(+) luminal-like layer and a CK5(+) basal-like layer. Notably, the numbers of spheres formed by inflamed and non-inflamed PSC were equal, suggesting that even though proliferation is enhanced by inflammation, the homeostatic level of PSC is maintained.

conclusionInduction of inflammation promotes PSC expansion and immediate differentiation through highly proliferative progenitor cells while the homeostasis of PSC is maintained.

Indexed as

AnimalsAutoimmunityCell ProliferationInflammationMaleMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicNeoplastic Stem CellsProstatic Neoplasmsinflammationprostate biologyprostate stem cells

Identifiers

PMID26174474
PMCPMC4720918
OpenAlexW1571877909

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.