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Fibroblast Growth Factor Family As a Potential Target in the Treatment of Hepatocellular Carcinoma

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Date 2016 Aug 11
PMID 27508175
Citations 4
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Abstract

Hepatocellular cancer (HCC) is currently the third leading cause of cancer death worldwide. The prognosis of patients diagnosed with late-stage disease is dismal due to high resistance to conventional systemic therapies. The introduction of sorafenib, despite its limited efficacy, as the standard systemic therapy for advanced HCC has paved a way for targeted molecular therapies for HCC. Fibroblast growth factor (FGF) signaling plays an important role in the developing embryo and the adult. The FGF signaling pathway is often hijacked by cancer cells, including HCC. Several alterations in FGF signaling correlate with poor outcome in HCC patients, suggesting that this family of signaling molecules plays an important role in the development of HCC. Multikinase inhibitors targeting FGF signaling are currently under investigation in clinical trials. This review discusses the current understanding of the biological and clinical implications of aberrant FGF signaling in the prognosis, diagnosis, and treatment of HCC.

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References
1.
Cao H, Phan H, Yang L . Improved chemotherapy for hepatocellular carcinoma. Anticancer Res. 2012; 32(4):1379-86. View

2.
Hughes S . Differential expression of the fibroblast growth factor receptor (FGFR) multigene family in normal human adult tissues. J Histochem Cytochem. 1997; 45(7):1005-19. DOI: 10.1177/002215549704500710. View

3.
Casanovas O, Hicklin D, Bergers G, Hanahan D . Drug resistance by evasion of antiangiogenic targeting of VEGF signaling in late-stage pancreatic islet tumors. Cancer Cell. 2005; 8(4):299-309. DOI: 10.1016/j.ccr.2005.09.005. View

4.
Llovet J, Decaens T, Raoul J, Boucher E, Kudo M, Chang C . Brivanib in patients with advanced hepatocellular carcinoma who were intolerant to sorafenib or for whom sorafenib failed: results from the randomized phase III BRISK-PS study. J Clin Oncol. 2013; 31(28):3509-16. DOI: 10.1200/JCO.2012.47.3009. View

5.
Hu M, Qiu W, Wang Y, Hill D, Ring B, Scully S . FGF-18, a novel member of the fibroblast growth factor family, stimulates hepatic and intestinal proliferation. Mol Cell Biol. 1998; 18(10):6063-74. PMC: 109192. DOI: 10.1128/MCB.18.10.6063. View