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Oncotarget. 2015 Apr 20;6(11):8454-73.

Targeting Hsp90 in urothelial carcinoma.

Author information

1
Department of Urology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
2
Department of Pathology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
3
Upstate Cancer Research Institute, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
4
Department of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.

Abstract

Urothelial carcinoma, or transitional cell carcinoma, is the most common urologic malignancy that carries significant morbidity, mortality, recurrence risk and associated health care costs. Despite use of current chemotherapies and immunotherapies, long-term remission in patients with muscle-invasive or metastatic disease remains low, and disease recurrence is common. The molecular chaperone Heat Shock Protein-90 (Hsp90) may offer an ideal treatment target, as it is a critical signaling hub in urothelial carcinoma pathogenesis and potentiates chemoradiation. Preclinical testing with Hsp90 inhibitors has demonstrated reduced proliferation, enhanced apoptosis and synergism with chemotherapies and radiation. Despite promising preclinical data, clinical trials utilizing Hsp90 inhibitors for other malignancies had modest efficacy. Therefore, we propose that Hsp90 inhibition would best serve as an adjuvant treatment in advanced muscle-invasive or metastatic bladder cancers to potentiate other therapies. An overview of bladder cancer biology, current treatments, molecular targeted therapies, and the role for Hsp90 inhibitors in the treatment of urothelial carcinoma is the focus of this review.

KEYWORDS:

Hsp90 inhibitors; bladder cancer treatments; heat shock protein-90; pathogenesis; urothelial carcinoma

PMID:
25909217
PMCID:
PMC4496161
DOI:
10.18632/oncotarget.3502
[Indexed for MEDLINE]
Free PMC Article

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