Evidence map›Paper›PMID 25895025›Full record

ArticleOncotarget2015

Infiltrating mast cells enhance prostate cancer invasion via altering LncRNA-HOTAIR/PRC2-androgen receptor (AR)-MMP9 signals and increased stem/progenitor cell population.

Lei Li, Qiang Dang, Hongjun Xie, Zhao Yang, Dalin He, Liang Liang, Wenbing Song, Shuyuan Yeh, Chawnshang Chang

Erratum issuedOpen access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 94 citations in OpenAlex.

  1. Human Group IIA Secreted Phospholipase AInternational journal of molecular sciences · 2026
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  18. LncRNAInternational journal of molecular sciences · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 3 countries.

Lei LiDepartment of Urology, Sex Hormone Research Center, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Qiang DangDepartment of Urology, Sex Hormone Research Center, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Hongjun XieDepartment of Urology, Sex Hormone Research Center, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Zhao YangDepartment of Urology, Sex Hormone Research Center, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Dalin HeDepartment of Urology, Sex Hormone Research Center, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Liang LiangDepartment of Urology, Sex Hormone Research Center, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Wenbing SongDepartment of Urology, Sex Hormone Research Center, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Shuyuan YehDepartments of Pathology and Urology, George Whipple Lab for Cancer Research, The Wilmot Cancer Center, University of Rochester Medical Center, Rochester, New York, USA.
Chawnshang ChangDepartments of Pathology and Urology, George Whipple Lab for Cancer Research, The Wilmot Cancer Center, University of Rochester Medical Center, Rochester, New York, USA.
Xi'an Jiaotong University · CNUniversity of Rochester Medical Center · USChina Medical University Hospital · TW

Funding

Non-AR mediated DHT-promoted Bladder Cancer initiation and progressionR01CA155477 · NCI · UNIVERSITY OF ROCHESTER · PI CHANG, CHAWNSHANG · 2011 to 2015
$1.6M
Stromal AR Roles in Prostate Hyperplasia and CancerR01CA156700 · NCI · UNIVERSITY OF ROCHESTER · PI CHANG, CHAWNSHANG, YEH, SHUYUAN · 2011 to 2015
$1.6M
NCI NIH HHS CA155477NCI NIH HHS CA156700NCI NIH HHS R01 CA155477NCI NIH HHS R01 CA156700
6 · The paper itself

Abstract

Early studies indicated that selective inflammatory immune cells in the prostate tumor microenvironment might be able to influence prostate cancer (PCa) progression. Here we found treating PCa cells with androgen deprivation therapy (ADT) results in the recruitment of more mast cells, which might then increase PCa cell invasion via down-regulation of AR signals in 4 different PCa cell lines. Mechanism dissection revealed infiltrating mast cells could decrease AR transcription via modulation of the PRC2 complex with LncRNA-HOTAIR at the AR 5' promoter region in PCa cells. The consequences of suppressing AR may then increase PCa cell invasion via increased MMP9 expression and/or increased stem/progenitor cell population. The in vivo mouse model with orthotopically xenografted PCa CWR22Rv1 cells with/without mast cells also confirmed that infiltrating mast cells could increase PCa cell invasion via suppression of AR signals. Together, our results provide a new mechanism for the ADT-enhanced PCa metastasis via altering the infiltrating mast cells to modulate PCa AR-MMP9 signals and/or AR-stem/progenitor cell population. Targeting these newly identified inflammatory mast cells-AR signals may help us to better suppress PCa metastasis at the castration resistant stage.

Indexed as

AnilidesAnimalsBenzamidesCell Line, TumorHeterograftsHumansMaleMAP Kinase Signaling SystemMast CellsMatrix Metalloproteinase 9MiceNeoplasm InvasivenessNeoplastic Stem CellsNitrilesPhenylthiohydantoinProstatic NeoplasmsAnilidesAR protein, humanBenzamidesbicalutamideenzalutamideHOTAIR long untranslated RNA, humanMatrix Metalloproteinase 9MMP9 protein, humanNitrilesPhenylthiohydantoinReceptors, AndrogenRNA, Long NoncodingTosyl Compoundsandrogen receptorHOTAIR-PRC2mast cellsprostate cancerstem cells

Identifiers

PMID25895025
PMCPMC4546459
OpenAlexW2131130559

What OpenQuestion holds

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Registered trials

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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.