Evidence map›Paper›PMID 36636689›Full record

ArticleAmerican journal of clinical and experimental urology2022

Stem cells from a malignant rat prostate cell line generate prostate cancers

Wen-Yang Hu, Li-Feng Liu, Parivash Afradiasbagharani, Ran-Li Lu, Zhen-Long Chen, Dan-Ping Hu, Lynn A Birch, Gail S Prins

Open access · greenAbstract read
In one paragraph

Article in American journal of clinical and experimental urology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 50% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Open veterinary journal · 2023
    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

8 authors at 2 institutions in 1 country.

Wen-Yang HuDepartment of Urology, University of Illinois at Chicago Chicago, IL 60612, USA.
Li-Feng LiuDepartment of Urology, University of Illinois at Chicago Chicago, IL 60612, USA.
Parivash AfradiasbagharaniDepartment of Urology, University of Illinois at Chicago Chicago, IL 60612, USA.
Ran-Li LuDepartment of Urology, University of Illinois at Chicago Chicago, IL 60612, USA.
Zhen-Long ChenDivision of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center Boston, MA 02215, USA.
Dan-Ping HuDepartment of Urology, University of Illinois at Chicago Chicago, IL 60612, USA.
Lynn A BirchDepartment of Urology, University of Illinois at Chicago Chicago, IL 60612, USA.
Gail S PrinsDepartment of Urology, University of Illinois at Chicago Chicago, IL 60612, USA.
University of Illinois Chicago · USBeth Israel Deaconess Medical Center · US

Funding

MiR-183-96-182 cluster, prostatic zinc homeostasis and carcinogenesisR01CA166588 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI NONN, LARISA · 2012 to 2016
$1.9M
Developmental Exposure to Low-dose Bisphenol A and Human Prostate Cancer SusceptiRC2ES018758 · NIEHS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI HO, SHUK-MEI, PRINS, GAIL S · 2009 to 2010
$1.9M
NCI NIH HHS R01 CA166588NIEHS NIH HHS RC2 ES018758
6 · The paper itself

Abstract

Cancer stem cells (CSCs) are resistant to conventional cancer therapies, permitting the repopulation of new tumor growth and driving disease progression. Models for testing prostate CSC-propagated tumor growth are presently limited yet necessary for therapeutic advancement. Utilizing the congenic nontumorigenic NRP152 and tumorigenic NRP154 rat prostate epithelial cell lines, the present study investigated the self-renewal, differentiation, and regenerative abilities of prostate stem/progenitor cells and developed a CSC-based PCa model. NRP154 cells expressed reduced levels of tumor suppressor caveolin-1 and increased p-Src as compared to NRP152 cells. Gene knockdown of caveolin-1 in NRP152 cells upregulated p-Src, implicating their role as potential oncogenic mediators in NRP154 cells. A FACS-based Hoechst exclusion assay revealed a side population of stem-like cells (0.1%) in both NRP152 and NRP154 cell lines. Using a 3D Matrigel culture system, stem cells from both cell lines established prostaspheres at a 0.1% efficiency through asymmetric self-renewal and rapid proliferation of daughter progenitor cells. Spheres derived from both cell lines contained CD117

Indexed as

cancer stem cellsprostasphereProstate cancer

Identifiers

PMID36636689
PMCPMC9831920
OpenAlexW4315928677

What OpenQuestion holds

Textmetadata
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.