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Lung Cancer Management with Silibinin: A Historical and Translational Perspective
The flavonolignan silibinin, the major bioactive component of the silymarin extract of Silybum marianum (milk thistle) seeds, is gaining traction as a novel anti-cancer therapeutic. Here, we review the historical developments that have laid the groundwork for the evaluation of silibinin as a chemopr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230811/ https://www.ncbi.nlm.nih.gov/pubmed/34208282 http://dx.doi.org/10.3390/ph14060559 |
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author | Verdura, Sara Cuyàs, Elisabet Ruiz-Torres, Verónica Micol, Vicente Joven, Jorge Bosch-Barrera, Joaquim Menendez, Javier A. |
author_facet | Verdura, Sara Cuyàs, Elisabet Ruiz-Torres, Verónica Micol, Vicente Joven, Jorge Bosch-Barrera, Joaquim Menendez, Javier A. |
author_sort | Verdura, Sara |
collection | PubMed |
description | The flavonolignan silibinin, the major bioactive component of the silymarin extract of Silybum marianum (milk thistle) seeds, is gaining traction as a novel anti-cancer therapeutic. Here, we review the historical developments that have laid the groundwork for the evaluation of silibinin as a chemopreventive and therapeutic agent in human lung cancer, including translational insights into its mechanism of action to control the aggressive behavior of lung carcinoma subtypes prone to metastasis. First, we summarize the evidence from chemically induced primary lung tumors supporting a role for silibinin in lung cancer prevention. Second, we reassess the preclinical and clinical evidence on the effectiveness of silibinin against drug resistance and brain metastasis traits of lung carcinomas. Third, we revisit the transcription factor STAT3 as a central tumor-cell intrinsic and microenvironmental target of silibinin in primary lung tumors and brain metastasis. Finally, by unraveling the selective vulnerability of silibinin-treated tumor cells to drugs using CRISPR-based chemosensitivity screenings (e.g., the hexosamine biosynthesis pathway inhibitor azaserine), we illustrate how the therapeutic use of silibinin against targetable weaknesses might be capitalized in specific lung cancer subtypes (e.g., KRAS/STK11 co-mutant tumors). Forthcoming studies should take up the challenge of developing silibinin and/or next-generation silibinin derivatives as novel lung cancer-preventive and therapeutic biomolecules. |
format | Online Article Text |
id | pubmed-8230811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82308112021-06-26 Lung Cancer Management with Silibinin: A Historical and Translational Perspective Verdura, Sara Cuyàs, Elisabet Ruiz-Torres, Verónica Micol, Vicente Joven, Jorge Bosch-Barrera, Joaquim Menendez, Javier A. Pharmaceuticals (Basel) Review The flavonolignan silibinin, the major bioactive component of the silymarin extract of Silybum marianum (milk thistle) seeds, is gaining traction as a novel anti-cancer therapeutic. Here, we review the historical developments that have laid the groundwork for the evaluation of silibinin as a chemopreventive and therapeutic agent in human lung cancer, including translational insights into its mechanism of action to control the aggressive behavior of lung carcinoma subtypes prone to metastasis. First, we summarize the evidence from chemically induced primary lung tumors supporting a role for silibinin in lung cancer prevention. Second, we reassess the preclinical and clinical evidence on the effectiveness of silibinin against drug resistance and brain metastasis traits of lung carcinomas. Third, we revisit the transcription factor STAT3 as a central tumor-cell intrinsic and microenvironmental target of silibinin in primary lung tumors and brain metastasis. Finally, by unraveling the selective vulnerability of silibinin-treated tumor cells to drugs using CRISPR-based chemosensitivity screenings (e.g., the hexosamine biosynthesis pathway inhibitor azaserine), we illustrate how the therapeutic use of silibinin against targetable weaknesses might be capitalized in specific lung cancer subtypes (e.g., KRAS/STK11 co-mutant tumors). Forthcoming studies should take up the challenge of developing silibinin and/or next-generation silibinin derivatives as novel lung cancer-preventive and therapeutic biomolecules. MDPI 2021-06-11 /pmc/articles/PMC8230811/ /pubmed/34208282 http://dx.doi.org/10.3390/ph14060559 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Verdura, Sara Cuyàs, Elisabet Ruiz-Torres, Verónica Micol, Vicente Joven, Jorge Bosch-Barrera, Joaquim Menendez, Javier A. Lung Cancer Management with Silibinin: A Historical and Translational Perspective |
title | Lung Cancer Management with Silibinin: A Historical and Translational Perspective |
title_full | Lung Cancer Management with Silibinin: A Historical and Translational Perspective |
title_fullStr | Lung Cancer Management with Silibinin: A Historical and Translational Perspective |
title_full_unstemmed | Lung Cancer Management with Silibinin: A Historical and Translational Perspective |
title_short | Lung Cancer Management with Silibinin: A Historical and Translational Perspective |
title_sort | lung cancer management with silibinin: a historical and translational perspective |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230811/ https://www.ncbi.nlm.nih.gov/pubmed/34208282 http://dx.doi.org/10.3390/ph14060559 |
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