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Molecular Signaling Pathways and Therapeutic Targets in Hepatocellular Carcinoma

Hepatocellular carcinoma (HCC) is a complex biological process and is often diagnosed at advanced stages with no effective treatment options. With advances in tumor biology and molecular genetic profiling, several different signaling pathways and molecular mechanisms have been identified as responsi...

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Autores principales: Dimri, Manali, Satyanarayana, Ande
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072513/
https://www.ncbi.nlm.nih.gov/pubmed/32093152
http://dx.doi.org/10.3390/cancers12020491
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author Dimri, Manali
Satyanarayana, Ande
author_facet Dimri, Manali
Satyanarayana, Ande
author_sort Dimri, Manali
collection PubMed
description Hepatocellular carcinoma (HCC) is a complex biological process and is often diagnosed at advanced stages with no effective treatment options. With advances in tumor biology and molecular genetic profiling, several different signaling pathways and molecular mechanisms have been identified as responsible for initiating and promoting HCC. Targeting these critical pathways, which include the receptor tyrosine kinase pathways, the Ras mitogen-activated protein kinase (Ras/Raf/MAPK), the phosphatidylinositol 3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR), the Wnt/β-catenin signaling pathway, the ubiquitin/proteasome degradation and the hedgehog signaling pathway has led to the identification of novel therapeutics for HCC treatment. In this review, we elaborated on our current understanding of the signaling pathways involved in the development and initiation of HCC and anticipate the potential targets for therapeutic drug development.
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spelling pubmed-70725132020-03-19 Molecular Signaling Pathways and Therapeutic Targets in Hepatocellular Carcinoma Dimri, Manali Satyanarayana, Ande Cancers (Basel) Review Hepatocellular carcinoma (HCC) is a complex biological process and is often diagnosed at advanced stages with no effective treatment options. With advances in tumor biology and molecular genetic profiling, several different signaling pathways and molecular mechanisms have been identified as responsible for initiating and promoting HCC. Targeting these critical pathways, which include the receptor tyrosine kinase pathways, the Ras mitogen-activated protein kinase (Ras/Raf/MAPK), the phosphatidylinositol 3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR), the Wnt/β-catenin signaling pathway, the ubiquitin/proteasome degradation and the hedgehog signaling pathway has led to the identification of novel therapeutics for HCC treatment. In this review, we elaborated on our current understanding of the signaling pathways involved in the development and initiation of HCC and anticipate the potential targets for therapeutic drug development. MDPI 2020-02-20 /pmc/articles/PMC7072513/ /pubmed/32093152 http://dx.doi.org/10.3390/cancers12020491 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Dimri, Manali
Satyanarayana, Ande
Molecular Signaling Pathways and Therapeutic Targets in Hepatocellular Carcinoma
title Molecular Signaling Pathways and Therapeutic Targets in Hepatocellular Carcinoma
title_full Molecular Signaling Pathways and Therapeutic Targets in Hepatocellular Carcinoma
title_fullStr Molecular Signaling Pathways and Therapeutic Targets in Hepatocellular Carcinoma
title_full_unstemmed Molecular Signaling Pathways and Therapeutic Targets in Hepatocellular Carcinoma
title_short Molecular Signaling Pathways and Therapeutic Targets in Hepatocellular Carcinoma
title_sort molecular signaling pathways and therapeutic targets in hepatocellular carcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072513/
https://www.ncbi.nlm.nih.gov/pubmed/32093152
http://dx.doi.org/10.3390/cancers12020491
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