Evidence map›Paper›PMID 26305549›Full record

ArticleOncotarget2015

Tumor microenvironment B cells increase bladder cancer metastasis via modulation of the IL-8/androgen receptor (AR)/MMPs signals.

Zhenyu Ou, Yongjie Wang, Longfei Liu, Lei Li, Shuyuan Yeh, Lin Qi, Chawnshang Chang

Open 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. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
5.6field-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

69 citing papers in PubMed, 115 citations in OpenAlex.

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  20. The androgen receptor in bladder cancer.Nature reviews. Urology · 2023
    Review

9 more citing papers are in PubMed but not listed here.

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

7 authors at 4 institutions in 3 countries.

Zhenyu OuDepartments of Urology and Plastic Surgery, Xiangya Hospital, Central South University, Changsha, China.
Yongjie WangDepartments of Urology and Plastic Surgery, Xiangya Hospital, Central South University, Changsha, China.
Longfei LiuDepartments of Urology and Plastic Surgery, Xiangya Hospital, Central South University, Changsha, China.
Lei LiGeorge Whipple Lab for Cancer Research, Departments of Pathology and Urology, University of Rochester Medical Center, Rochester, NY, USA.
Shuyuan YehGeorge Whipple Lab for Cancer Research, Departments of Pathology and Urology, University of Rochester Medical Center, Rochester, NY, USA.
Lin QiDepartments of Urology and Plastic Surgery, Xiangya Hospital, Central South University, Changsha, China.
Chawnshang ChangGeorge Whipple Lab for Cancer Research, Departments of Pathology and Urology, University of Rochester Medical Center, Rochester, NY, USA.
University of Rochester Medical Center · USCentral South University · CNChina Medical University · TWXiangya Hospital Central South University · CN

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

While B cells in the tumor microenvironment may play important roles in cancer progression, their impacts on the bladder cancer (BCa) metastasis remain unclear. Here we found from human clinical BCa samples that BCa tissues could recruit more B cells than the surrounding normal bladder tissues and the in vitro co-culture assay also demonstrated that B cells could be recruited more easily towards BCa cells compared to normal bladder cells. Chamber invasion and 3D invasion assays showed the recruited B cells could then significantly increase the BCa cell invasion. Mechanism dissection found that recruited B cells could increase IL-8/androgen receptor (AR) signals in BCa cells that could then promote the expression of metastasis genes including MMP1 and MMP13. Blocking the IL-8/AR/MMPs signals either by anti-IL-8 neutralizing antibody, AR-siRNA, or MMPs inhibitors all partially reversed the infiltrating B cells capacity to increase the BCa cell invasion. The in vivo data from orthotopically xenografted BCa mouse model also confirmed that infiltrating B cells could increase BCa cell invasion via increasing AR signals. Together, these results demonstrate the key roles of B cells within the bladder tumor microenvironment that increase the BCa metastasis and may help us to develop the potential therapies via targeting these newly identified IL-8/AR/MMPs signals to better battle the BCa progression.

Indexed as

AnimalsBlotting, WesternB-LymphocytesCell Line, TumorCell MovementCells, CulturedCoculture TechniquesGene Expression Regulation, NeoplasticHumansInterleukin-8MaleMatrix Metalloproteinase 1Matrix Metalloproteinase 13Matrix Metalloproteinase InhibitorsMatrix MetalloproteinasesMice, NudeAR protein, humanInterleukin-8Matrix Metalloproteinase 1Matrix Metalloproteinase 13Matrix Metalloproteinase InhibitorsMatrix MetalloproteinasesReceptors, Androgenandrogen receptorB cellbladder cancertumor metastasistumor microenvironment

Identifiers

PMID26305549
PMCPMC4694886
OpenAlexW2129078297

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.