Mechanisms of Pharmacoresistance in Hepatocellular Carcinoma: New Drugs but Old Problems

Author:

Marin Jose J.G.12,Romero Marta R.12,Herraez Elisa12,Asensio Maitane12,Ortiz-Rivero Sara1,Sanchez-Martin Anabel1,Fabris Luca34,Briz Oscar12

Affiliation:

1. Experimental Hepatology and Drug Targeting (HEVEPHARM), University of Salamanca, IBSAL, Salamanca, Spain

2. Center for the Study of Liver and Gastrointestinal Diseases (CIBERehd), Carlos III National Institute of Health, Madrid, Spain

3. Department of Molecular Medicine (DMM), University of Padua, Padua, Italy

4. Department of Internal Medicine, Yale Liver Center (YLC), School of Medicine, Yale University New Haven, Connecticut

Abstract

AbstractHepatocellular carcinoma (HCC) is a malignancy with poor prognosis when diagnosed at advanced stages in which curative treatments are no longer applicable. A small group of these patients may still benefit from transarterial chemoembolization. The only therapeutic option for most patients with advanced HCC is systemic pharmacological treatments based on tyrosine kinase inhibitors (TKIs) and immunotherapy. Available drugs only slightly increase survival, as tumor cells possess additive and synergistic mechanisms of pharmacoresistance (MPRs) prior to or enhanced during treatment. Understanding the molecular basis of MPRs is crucial to elucidate the genetic signature underlying HCC resistome. This will permit the selection of biomarkers to predict drug treatment response and identify tumor weaknesses in a personalized and dynamic way. In this article, we have reviewed the role of MPRs in current first-line drugs and the combinations of immunotherapeutic agents with novel TKIs being tested in the treatment of advanced HCC.

Funder

Centro Internacional sobre el Envejecimiento, Spain

Fundació Marato TV3, Spain

Fundación Científica Asociación Española Contra el Cáncer

Ministerio de Economía y Competitividad; Instituto de Salud Carlos III

Junta de Castilla y León

Publisher

Georg Thieme Verlag KG

Subject

Hepatology

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