4.6 Article

Sorafenib-based combined molecule targeting in treatment of hepatocellular carcinoma

Journal

WORLD JOURNAL OF GASTROENTEROLOGY
Volume 21, Issue 42, Pages 12059-12070

Publisher

BAISHIDENG PUBLISHING GROUP INC
DOI: 10.3748/wjg.v21.i42.12059

Keywords

Angiogenesis; Mammalian target of rapamycin; Extracellular-signal regulated kinase; Endothelial growth factor receptor; Histone deacetylases

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Sorafenib is the only and standard systematic chemotherapy drug for treatment of advanced hepato-cellular carcinoma (HCC) at the current stage. Although sorafenib showed survival benefits in large randomized phase. studies, its clinical benefits remain modest and most often consist of temporary tumor stabilization, indicating that more effective first-line treatment regimens or second-line salvage therapies are required. The molecular pathogenesis of HCC is very complex, involving hyperactivated signal transduction pathways such as RAS/RAF/MEK/ERK and PI3K/AKT/mTOR and aberrant expression of molecules such as receptor tyrosine kinases and histone deacetylases. Simultaneous or sequential abrogation of these critical pathways or the functions of these key molecules involved in angiogenesis, proliferation, and apoptosis may yield major improvements in the management of HCC. In this review, we summarize the emerging sorafenib-based combined molecule targeting for HCC treatment and analyze the rationales of these combinations.

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