Cargando…

A Novel Indication for Panobinostat as a Senolytic Drug in NSCLC and HNSCC

Panobinostat (pano) is an FDA-approved histone deacetylase inhibitor. There is interest in evaluating alternate dosing schedules and novel combinations of pano for the treatment of upper aerodigestive and lung malignancies; thus we evaluated it in combination with Taxol, a chemotherapeutic with acti...

Descripción completa

Detalles Bibliográficos
Autores principales: Samaraweera, Leleesha, Adomako, Alfred, Rodriguez-Gabin, Alicia, McDaid, Hayley M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432488/
https://www.ncbi.nlm.nih.gov/pubmed/28507307
http://dx.doi.org/10.1038/s41598-017-01964-1
_version_ 1783236636456255488
author Samaraweera, Leleesha
Adomako, Alfred
Rodriguez-Gabin, Alicia
McDaid, Hayley M.
author_facet Samaraweera, Leleesha
Adomako, Alfred
Rodriguez-Gabin, Alicia
McDaid, Hayley M.
author_sort Samaraweera, Leleesha
collection PubMed
description Panobinostat (pano) is an FDA-approved histone deacetylase inhibitor. There is interest in evaluating alternate dosing schedules and novel combinations of pano for the treatment of upper aerodigestive and lung malignancies; thus we evaluated it in combination with Taxol, a chemotherapeutic with activity in both diseases. Dose-dependent synergy was observed in Non-Small Cell Lung Cancer (NSCLC) and Head and Neck Squamous Cell Carcinoma (HNSCC) cell lines and was due to senescence rather than potentiation of cell death. Senescence occurred following cisplatin- or Taxol-treatment in cell lines from both cancer types and was associated with decreased histone 3 (H3) acetylation and increased Bcl-xL expression: the latter a biomarker of senescence and target of anti-senescence therapeutics, or senolytics. Since H3 acetylation and Bcl-xL expression were altered in senescence, we subsequently evaluated pano as a senolytic in chemotherapy-treated cancer cells enriched for senescent cells. Pano caused cell death at significantly higher rates compared to repeat dosing with chemotherapy. This was associated with decreased expression of Bcl-xL and increased acetylated H3, reversing the expression patterns observed in senescence. These data support evaluating pano as a post-chemotherapy senolytic with the potential to kill persistent senescent cells that accumulate during standard chemotherapy in NSCLC and HNSCC.
format Online
Article
Text
id pubmed-5432488
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-54324882017-05-16 A Novel Indication for Panobinostat as a Senolytic Drug in NSCLC and HNSCC Samaraweera, Leleesha Adomako, Alfred Rodriguez-Gabin, Alicia McDaid, Hayley M. Sci Rep Article Panobinostat (pano) is an FDA-approved histone deacetylase inhibitor. There is interest in evaluating alternate dosing schedules and novel combinations of pano for the treatment of upper aerodigestive and lung malignancies; thus we evaluated it in combination with Taxol, a chemotherapeutic with activity in both diseases. Dose-dependent synergy was observed in Non-Small Cell Lung Cancer (NSCLC) and Head and Neck Squamous Cell Carcinoma (HNSCC) cell lines and was due to senescence rather than potentiation of cell death. Senescence occurred following cisplatin- or Taxol-treatment in cell lines from both cancer types and was associated with decreased histone 3 (H3) acetylation and increased Bcl-xL expression: the latter a biomarker of senescence and target of anti-senescence therapeutics, or senolytics. Since H3 acetylation and Bcl-xL expression were altered in senescence, we subsequently evaluated pano as a senolytic in chemotherapy-treated cancer cells enriched for senescent cells. Pano caused cell death at significantly higher rates compared to repeat dosing with chemotherapy. This was associated with decreased expression of Bcl-xL and increased acetylated H3, reversing the expression patterns observed in senescence. These data support evaluating pano as a post-chemotherapy senolytic with the potential to kill persistent senescent cells that accumulate during standard chemotherapy in NSCLC and HNSCC. Nature Publishing Group UK 2017-05-15 /pmc/articles/PMC5432488/ /pubmed/28507307 http://dx.doi.org/10.1038/s41598-017-01964-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Samaraweera, Leleesha
Adomako, Alfred
Rodriguez-Gabin, Alicia
McDaid, Hayley M.
A Novel Indication for Panobinostat as a Senolytic Drug in NSCLC and HNSCC
title A Novel Indication for Panobinostat as a Senolytic Drug in NSCLC and HNSCC
title_full A Novel Indication for Panobinostat as a Senolytic Drug in NSCLC and HNSCC
title_fullStr A Novel Indication for Panobinostat as a Senolytic Drug in NSCLC and HNSCC
title_full_unstemmed A Novel Indication for Panobinostat as a Senolytic Drug in NSCLC and HNSCC
title_short A Novel Indication for Panobinostat as a Senolytic Drug in NSCLC and HNSCC
title_sort novel indication for panobinostat as a senolytic drug in nsclc and hnscc
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432488/
https://www.ncbi.nlm.nih.gov/pubmed/28507307
http://dx.doi.org/10.1038/s41598-017-01964-1
work_keys_str_mv AT samaraweeraleleesha anovelindicationforpanobinostatasasenolyticdruginnsclcandhnscc
AT adomakoalfred anovelindicationforpanobinostatasasenolyticdruginnsclcandhnscc
AT rodriguezgabinalicia anovelindicationforpanobinostatasasenolyticdruginnsclcandhnscc
AT mcdaidhayleym anovelindicationforpanobinostatasasenolyticdruginnsclcandhnscc
AT samaraweeraleleesha novelindicationforpanobinostatasasenolyticdruginnsclcandhnscc
AT adomakoalfred novelindicationforpanobinostatasasenolyticdruginnsclcandhnscc
AT rodriguezgabinalicia novelindicationforpanobinostatasasenolyticdruginnsclcandhnscc
AT mcdaidhayleym novelindicationforpanobinostatasasenolyticdruginnsclcandhnscc