| Literature DB >> 27381494 |
Erica di Martino1, Darren C Tomlinson2, Sarah V Williams1, Margaret A Knowles1.
Abstract
Bladder tumors show diverse molecular features and clinical outcome. Muscle-invasive bladder cancer has poor prognosis and novel approaches to systemic therapy are urgently required. Non-muscle-invasive bladder cancer has good prognosis, but high recurrence rate and the requirement for life-long disease monitoring places a major burden on patients and healthcare providers. Studies of tumor tissues from both disease groups have identified frequent alterations of FGFRs, including mutations of FGFR3 and dysregulated expression of FGFR1 and FGFR3 that suggest that these may be valid therapeutic targets. We summarize current understanding of the molecular alterations affecting these receptors in bladder tumors, preclinical studies validating them as therapeutic targets, available FGFR-targeted agents and results from early clinical trials in bladder cancer patients.Entities:
Keywords: FGFR1; FGFR3; FGFRs; bladder; cancer; targeted therapy; urothelial
Mesh:
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Year: 2016 PMID: 27381494 PMCID: PMC5066128 DOI: 10.2217/fon-2016-0042
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404