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Targeting the FGFR signaling pathway in cholangiocarcinoma: promise or delusion?
- Source :
- Therapeutic Advances in Medical Oncology, Vol 12 (2020), Therapeutic Advances in Medical Oncology
- Publication Year :
- 2020
- Publisher :
- SAGE Publishing, 2020.
-
Abstract
- Cholangiocarcinoma (CCA) is a refractory cancer with limited treatment options and poorly understood molecular mechanisms underlying tumor development. The most effective treatment is surgical resection; however, patients are highly prone to recurrence. Moreover, considering that most patients are diagnosed in advanced stages, treatment options are restricted to palliative care, which results in poor prognosis. Due to the limited effect of chemotherapy and radiotherapy, targeted therapy is becoming a hot topic in the field of biliary cancer treatment. The fibroblast growth factor/fibroblast growth factor receptor (FGF/FGFR) signaling pathway involves a variety of key biological processes for cell survival, differentiation, and metabolism. Next-generation sequencing data mining has shown that high levels of FGF/FGFR expression are associated with reduced overall survival (OS) in CAA, which indicates that the FGF/FGFR pathway may be an effective target for CAA treatment. This paper reviews the effect of FGF/FGFR signaling on CCA from onset to treatment and highlights the promise of FGF/FGFR signaling pathway inhibitors for targeting CCA.
- Subjects :
- Chemotherapy
Palliative care
FGFR signaling pathway
business.industry
medicine.medical_treatment
Review
Fibroblast growth factor
targeted therapy
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
lcsh:RC254-282
Targeted therapy
Radiation therapy
Oncology
Fibroblast growth factor receptor
fibroblast growth factor receptor
tyrosine kinase inhibitors
medicine
Cancer research
Signal transduction
business
cholangiocarcinoma
Subjects
Details
- Language :
- English
- ISSN :
- 17588359
- Volume :
- 12
- Database :
- OpenAIRE
- Journal :
- Therapeutic Advances in Medical Oncology
- Accession number :
- edsair.doi.dedup.....00e031583eb26d261beccd94e2d5a4cf