| dc.contributor.author | García Marín, José Juan | |
| dc.contributor.author | Rodríguez Romero, Marta | |
| dc.contributor.author | Herráez Aguilar, Elisa | |
| dc.contributor.author | Arsensio Martín, Maitane | |
| dc.contributor.author | Ortiz-Rivero, Sara | |
| dc.contributor.author | Sánchez Martín, Anabel | |
| dc.contributor.author | Fabris, Luca | |
| dc.contributor.author | Briz Sánchez, Oscar | |
| dc.date.accessioned | 2025-01-30T11:30:55Z | |
| dc.date.available | 2025-01-30T11:30:55Z | |
| dc.date.issued | 2021 | |
| dc.identifier.citation | Marin, J. J. G., Romero, M. R., Herraez, E., Asensio, M., Ortiz-Rivero, S., Sanchez-Martin, A., Fabris, L., y Briz, O. (2022). Mechanisms of pharmacoresistance in hepatocellular carcinoma: New drugs but old problems. Seminars in Liver Disease, 42(01), 087-103. https://doi.org/10.1055/s-0041-1735631 | es_ES |
| dc.identifier.issn | 0272-8087 | |
| dc.identifier.uri | http://hdl.handle.net/10366/163200 | |
| dc.description.abstract | Hepatocellular carcinoma (HCC) is a malignancy with poor prognosis when diagnosed at advanced stages in which curative treatments are no longer applicable.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. | es_ES |
| dc.language.iso | eng | es_ES |
| dc.publisher | Thieme Gruppe | es_ES |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
| dc.subject | Immunotherapy | es_ES |
| dc.subject | Liver cancer | es_ES |
| dc.subject | Multidrug resistance | es_ES |
| dc.subject | Targeted therapy | es_ES |
| dc.subject.mesh | Immunotherapy | * |
| dc.subject.mesh | Liver Neoplasms | * |
| dc.subject.mesh | Molecular Targeted Therapy | * |
| dc.subject.mesh | Multidrug Resistance-Associated Proteins | * |
| dc.title | Mechanisms of Pharmacoresistance in Hepatocellular Carcinoma: New Drugs but Old Problems | es_ES |
| dc.type | info:eu-repo/semantics/article | es_ES |
| dc.relation.publishversion | https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0041-1735631 | es_ES |
| dc.subject.unesco | 3201.01 Oncología | es_ES |
| dc.identifier.doi | 10.1055/s-0041-1735631 | |
| dc.rights.accessRights | info:eu-repo/semantics/closedAccess | es_ES |
| dc.identifier.essn | 1098-8971 | |
| dc.journal.title | Seminars in Liver Disease | es_ES |
| dc.volume.number | 42 | es_ES |
| dc.issue.number | 01 | es_ES |
| dc.page.initial | 087 | es_ES |
| dc.page.final | 103 | es_ES |
| dc.type.hasVersion | info:eu-repo/semantics/publishedVersion | es_ES |
| dc.subject.decs | terapia molecular selectiva | * |
| dc.subject.decs | neoplasias hepáticas | * |
| dc.subject.decs | inmunoterapia | * |
| dc.subject.decs | proteínas asociadas a la resistencia multimedicamentosa | * |
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