Evidence map›Paper›PMID 27186399›Full record

ArticleAmerican journal of cancer research2016

Androgen receptor expands the population of cancer stem cells in upper urinary tract urothelial cell carcinoma cells.

Chi-Cheng Chen, Teng-Fu Hsieh, Chi-Ping Huang, Ai-Lin Yu, Wen-Lin Chang, Chih-Rong Shyr

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
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  3. Review
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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

6 authors at 1 institution in 2 countries.

Chi-Cheng ChenSex Hormone Research Center, Departments of Urology/Surgery and Medical Laboratory Science and Biotechnology, Graduate Institute of Clinical Medical Science, China Medical University/HospitalTaichung 404, Taiwan; Department of Urology, Taichung Tzu Chi Hospital, Buddhist Tzu Chi Medical FoundationTaichung 404, Taiwan.
Teng-Fu HsiehSex Hormone Research Center, Departments of Urology/Surgery and Medical Laboratory Science and Biotechnology, Graduate Institute of Clinical Medical Science, China Medical University/HospitalTaichung 404, Taiwan; Department of Urology, Taichung Tzu Chi Hospital, Buddhist Tzu Chi Medical FoundationTaichung 404, Taiwan.
Chi-Ping HuangSex Hormone Research Center, Departments of Urology/Surgery and Medical Laboratory Science and Biotechnology, Graduate Institute of Clinical Medical Science, China Medical University/Hospital Taichung 404, Taiwan.
Ai-Lin YuSex Hormone Research Center, Departments of Urology/Surgery and Medical Laboratory Science and Biotechnology, Graduate Institute of Clinical Medical Science, China Medical University/Hospital Taichung 404, Taiwan.
Wen-Lin ChangSex Hormone Research Center, Departments of Urology/Surgery and Medical Laboratory Science and Biotechnology, Graduate Institute of Clinical Medical Science, China Medical University/Hospital Taichung 404, Taiwan.
Chih-Rong ShyrSex Hormone Research Center, Departments of Urology/Surgery and Medical Laboratory Science and Biotechnology, Graduate Institute of Clinical Medical Science, China Medical University/Hospital Taichung 404, Taiwan.
China Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Androgen receptor (AR) affects the development and progression of upper urinary tract urothelial cell carcinoma (UUTUC). However, the regulatory mechanism exerted by AR to affect UUTUC cells remains unclear. Here we investigated whether AR promotes UUTUC development and progression, possibly by expanding the population of cancer stem cells (CSCs), which are a particular population of cells within cancer cells responsible for tumor initiation, drug resistance and metastasis. We compared UUTUC cells with or without the addition of AR on their CSC population with flow cytometry, colony formation and sphere formation assay to determine the effect of AR on CSC activity, and real-time PCR was used to detect the expression stemness genes and miRNAs. In vivo tumor formation was evaluated with the implantation of cancer cells in nude mice. We found that the addition of AR in UUTUC cells, significantly increased the population of CSC, clonogenicity, sphere formation and the expression of stemness genes (Oct4, Bmi1 and Nanog), altered CSC-related miRNA profile, as well as promoted epithelial mesenchymal transition (EMT). And AR inhibitor, enzalutamide was shown to suppress AR's effect on tumorsphere formation. Furthermore, in an immune-deficient mouse model, the addition of AR in UUTUC cells also increased the tumor formation capacity. This study will help us better understand the extent to which AR contributes to UUTUC progression by expanding their CSC population and capacity. Our findings could explain high incidence of UUTUC observed in males. And targeting AR may lead to novel therapeutic approaches for genetically diversified urothelial carcinomas in precision medicine era.

Indexed as

Androgen receptorcancer stem cellstumorsphereupper urinary tract urothelial cell carcinoma

Identifiers

PMID27186399
PMCPMC4859656
OpenAlexW2398712462

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.