Androgen Receptor Signaling Reduces the Efficacy of Bacillus Calmette-Guérin Therapy for Bladder Cancer via Modulating Rab27b-Induced Exocytosis.


Journal

Molecular cancer therapeutics
ISSN: 1538-8514
Titre abrégé: Mol Cancer Ther
Pays: United States
ID NLM: 101132535

Informations de publication

Date de publication:
09 2020
Historique:
received: 21 01 2020
revised: 24 06 2020
accepted: 01 07 2020
pubmed: 2 8 2020
medline: 6 11 2020
entrez: 2 8 2020
Statut: ppublish

Résumé

Although intravesical bacillus Calmette-Guérin (BCG) immunotherapy has been the gold standard for nonsurgical management of non-muscle-invasive bladder cancer, a considerable number of patients exhibit resistance to the adjuvant treatment with unexplained mechanisms. This study aimed to investigate whether and how androgen receptor (AR) signals modulate BCG cytotoxicity in bladder cancer. AR knockdown or overexpression in bladder cancer lines resulted in induction or reduction, respectively, in intracellular BCG quantity and its cytotoxic activity. Microarray screening identified Rab27b, a small GTPase known to mediate bacterial exocytosis, which was upregulated in BCG-resistant cells and downregulated in AR-shRNA cells. Knockdown of Rab27b, or its effector SYTL3, or overexpression of Rab27b also induced or reduced, respectively, BCG quantity and cytotoxicity. In addition, treatment with GW4869, which was previously shown to inhibit Rab27b-dependent secretion, induced them and reduced Rab27b expression in bladder cancer cells. Meanwhile, AR expression was upregulated in BCG-resistant lines, compared with respective controls. In a mouse orthotopic xenograft model, Rab27b/SYTL3 knockdown or GW4869 treatment enhanced the amount of BCG within tumors and its suppressive effect on tumor growth. Moreover, in non-muscle-invasive bladder cancer specimens from patients subsequently undergoing BCG therapy, positivity of AR/Rab27b expression was associated with significantly higher risks of tumor recurrence. AR activation thus correlates with resistance to BCG treatment, presumably via upregulating Rab27b expression. Mechanistically, it is suggested that BCG elimination from urothelial cells is induced by Rab27b/SYTL3-mediated exocytosis. Accordingly, Rab27b inactivation, potentially via antiandrogenic drugs and/or exocytosis inhibition are anticipated to sensitize the efficacy of BCG therapy, especially in patients with BCG-refractory AR/Rab27b-positive bladder cancer.

Identifiants

pubmed: 32737155
pii: 1535-7163.MCT-20-0050
doi: 10.1158/1535-7163.MCT-20-0050
doi:

Substances chimiques

AR protein, human 0
BCG Vaccine 0
Receptors, Androgen 0
Rab27B protein, human EC 3.6.1.-.
rab GTP-Binding Proteins EC 3.6.5.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1930-1942

Informations de copyright

©2020 American Association for Cancer Research.

Auteurs

Taichi Mizushima (T)

Department of Pathology & Laboratory Medicine, University of Rochester Medical Center, Rochester, New York.
James P. Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, New York.
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Obstetrics and Gynecology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

Guiyang Jiang (G)

Department of Pathology & Laboratory Medicine, University of Rochester Medical Center, Rochester, New York.
James P. Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, New York.

Takashi Kawahara (T)

Department of Pathology & Laboratory Medicine, University of Rochester Medical Center, Rochester, New York.
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Departments of Urology and Renal Transplantation, Yokohama City University Medical Center, Yokohama, Japan.

Peng Li (P)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Bin Han (B)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Satoshi Inoue (S)

Department of Pathology & Laboratory Medicine, University of Rochester Medical Center, Rochester, New York.
James P. Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, New York.
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Hiroki Ide (H)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Ikuma Kato (I)

Department of Molecular Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

Mehrsa Jalalizadeh (M)

James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Etsuko Miyagi (E)

Department of Obstetrics and Gynecology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

Mitsunori Fukuda (M)

Department of Integrative Life Sciences, Tohoku University Graduate School of Life Sciences, Sendai, Japan.

Leonardo O Reis (LO)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Hiroshi Miyamoto (H)

Department of Pathology & Laboratory Medicine, University of Rochester Medical Center, Rochester, New York. hiroshi_miyamoto@urmc.rochester.edu.
James P. Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, New York.
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Urology, University of Rochester Medical Center, Rochester, New York.

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Classifications MeSH