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Potential synergistic effect of phosphodiesterase inhibitors with chemotherapy in lung cancer

Purpose: Lung cancer remains the leading cause of cancer-related deaths worldwide and novel therapeutic approaches targeting crucial pathways are urgently needed to improve its treatment. Differentiation-based therapeutics (Methylxanthines) and phosphodiesterase inhibitors (type 4 and 5), have been...

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Autores principales: Domvri, Kalliopi, Zarogoulidis, Konstantinos, Zogas, Nikolaos, Zarogoulidis, Paul, Petanidis, Savvas, Porpodis, Konstantinos, Kioseoglou, Efrosini, Hohenforst-Schmidt, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2017
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688917/
https://www.ncbi.nlm.nih.gov/pubmed/29151951
http://dx.doi.org/10.7150/jca.21783
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author Domvri, Kalliopi
Zarogoulidis, Konstantinos
Zogas, Nikolaos
Zarogoulidis, Paul
Petanidis, Savvas
Porpodis, Konstantinos
Kioseoglou, Efrosini
Hohenforst-Schmidt, Wolfgang
author_facet Domvri, Kalliopi
Zarogoulidis, Konstantinos
Zogas, Nikolaos
Zarogoulidis, Paul
Petanidis, Savvas
Porpodis, Konstantinos
Kioseoglou, Efrosini
Hohenforst-Schmidt, Wolfgang
author_sort Domvri, Kalliopi
collection PubMed
description Purpose: Lung cancer remains the leading cause of cancer-related deaths worldwide and novel therapeutic approaches targeting crucial pathways are urgently needed to improve its treatment. Differentiation-based therapeutics (Methylxanthines) and phosphodiesterase inhibitors (type 4 and 5), have been implicated in cancer treatment. Our objectives were to capture any potential anti-tumor effect of these drug combinations with chemotherapeutic agents in vitro. Methods: Theophylline as Methylxanthines, Roflumilast as phosphodiesterase type 4 (PDE4) inhibitor and Sildenafil as phosphodiesterase type 5 (PDE5) inhibitor are the drugs that we combined with the chemotherapeutic agents (Docetaxel, Cisplatin and Carboplatin) in vitro. Lung cancer cell lines (NCI-H1048-Small cell lung cancer-SCLC, A549- Non-small cell lung cancer-NSCLC) were purchased from ATCC LGC Standards. At indicated time-point, following 24h and 48h incubation, cell viability and apoptosis were measured with Annexin V staining by flow cytometry. Statistical analysis was performed by GraphPad Prism. Results: In SCLC, following 48h incubation, platinum combinations of carboplatin with roflumilast and sildenafil (p<0.001) and carboplatin with theophylline and sildenafil showed increased apoptosis when compared to carboplatin alone. Concerning the combinations of cisplatin, when combined with roflumilast, theophylline and sildenafil appeared with increased apoptosis of that alone (p<0.001, 24h and 48h incubation). In NSCLC, the 24h incubation was not enough to induce satisfactory apoptosis, except for the combination of cisplatin with roflumilast and theophylline (p<0.05) when compared to cisplatin alone. However, following 48h incubation, carboplatin plus sildenafil, carboplatin plus sildenafil, theophylline and roflumilast showed more cytotoxicity when compared to carboplatin alone (p<0.001). Docetaxel combinations showed no statistically significant results. Conclusion: The synergistic effect of PDE inhibitors with platinum-based agents has been demonstrated in lung cancer. Our suggestion is that these combinations could be used as additive and maintenance treatment in combination to antineoplastic agents in lung cancer patients.
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spelling pubmed-56889172017-11-18 Potential synergistic effect of phosphodiesterase inhibitors with chemotherapy in lung cancer Domvri, Kalliopi Zarogoulidis, Konstantinos Zogas, Nikolaos Zarogoulidis, Paul Petanidis, Savvas Porpodis, Konstantinos Kioseoglou, Efrosini Hohenforst-Schmidt, Wolfgang J Cancer Research Paper Purpose: Lung cancer remains the leading cause of cancer-related deaths worldwide and novel therapeutic approaches targeting crucial pathways are urgently needed to improve its treatment. Differentiation-based therapeutics (Methylxanthines) and phosphodiesterase inhibitors (type 4 and 5), have been implicated in cancer treatment. Our objectives were to capture any potential anti-tumor effect of these drug combinations with chemotherapeutic agents in vitro. Methods: Theophylline as Methylxanthines, Roflumilast as phosphodiesterase type 4 (PDE4) inhibitor and Sildenafil as phosphodiesterase type 5 (PDE5) inhibitor are the drugs that we combined with the chemotherapeutic agents (Docetaxel, Cisplatin and Carboplatin) in vitro. Lung cancer cell lines (NCI-H1048-Small cell lung cancer-SCLC, A549- Non-small cell lung cancer-NSCLC) were purchased from ATCC LGC Standards. At indicated time-point, following 24h and 48h incubation, cell viability and apoptosis were measured with Annexin V staining by flow cytometry. Statistical analysis was performed by GraphPad Prism. Results: In SCLC, following 48h incubation, platinum combinations of carboplatin with roflumilast and sildenafil (p<0.001) and carboplatin with theophylline and sildenafil showed increased apoptosis when compared to carboplatin alone. Concerning the combinations of cisplatin, when combined with roflumilast, theophylline and sildenafil appeared with increased apoptosis of that alone (p<0.001, 24h and 48h incubation). In NSCLC, the 24h incubation was not enough to induce satisfactory apoptosis, except for the combination of cisplatin with roflumilast and theophylline (p<0.05) when compared to cisplatin alone. However, following 48h incubation, carboplatin plus sildenafil, carboplatin plus sildenafil, theophylline and roflumilast showed more cytotoxicity when compared to carboplatin alone (p<0.001). Docetaxel combinations showed no statistically significant results. Conclusion: The synergistic effect of PDE inhibitors with platinum-based agents has been demonstrated in lung cancer. Our suggestion is that these combinations could be used as additive and maintenance treatment in combination to antineoplastic agents in lung cancer patients. Ivyspring International Publisher 2017-10-09 /pmc/articles/PMC5688917/ /pubmed/29151951 http://dx.doi.org/10.7150/jca.21783 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Domvri, Kalliopi
Zarogoulidis, Konstantinos
Zogas, Nikolaos
Zarogoulidis, Paul
Petanidis, Savvas
Porpodis, Konstantinos
Kioseoglou, Efrosini
Hohenforst-Schmidt, Wolfgang
Potential synergistic effect of phosphodiesterase inhibitors with chemotherapy in lung cancer
title Potential synergistic effect of phosphodiesterase inhibitors with chemotherapy in lung cancer
title_full Potential synergistic effect of phosphodiesterase inhibitors with chemotherapy in lung cancer
title_fullStr Potential synergistic effect of phosphodiesterase inhibitors with chemotherapy in lung cancer
title_full_unstemmed Potential synergistic effect of phosphodiesterase inhibitors with chemotherapy in lung cancer
title_short Potential synergistic effect of phosphodiesterase inhibitors with chemotherapy in lung cancer
title_sort potential synergistic effect of phosphodiesterase inhibitors with chemotherapy in lung cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688917/
https://www.ncbi.nlm.nih.gov/pubmed/29151951
http://dx.doi.org/10.7150/jca.21783
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