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No Causal Link between Phosphodiesterase Type 5 Inhibition and Melanoma

PURPOSE: To examine the association between phosphodiesterase type 5 (PDE5) inhibitor use and melanoma by 1) conducting a systematic review of observational studies; and 2) determining if low PDE5A gene expression in human melanoma correlated with decreased overall survival. MATERIALS AND METHODS: A...

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Autores principales: Wang, Jenny Z., Le, Stephanie, Alexanian, Claire, Boddu, Sucharita, Merleev, Alexander, Marusina, Alina, Maverakis, Emanual
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Sexual Medicine and Andrology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704303/
https://www.ncbi.nlm.nih.gov/pubmed/30350485
http://dx.doi.org/10.5534/wjmh.180050
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author Wang, Jenny Z.
Le, Stephanie
Alexanian, Claire
Boddu, Sucharita
Merleev, Alexander
Marusina, Alina
Maverakis, Emanual
author_facet Wang, Jenny Z.
Le, Stephanie
Alexanian, Claire
Boddu, Sucharita
Merleev, Alexander
Marusina, Alina
Maverakis, Emanual
author_sort Wang, Jenny Z.
collection PubMed
description PURPOSE: To examine the association between phosphodiesterase type 5 (PDE5) inhibitor use and melanoma by 1) conducting a systematic review of observational studies; and 2) determining if low PDE5A gene expression in human melanoma correlated with decreased overall survival. MATERIALS AND METHODS: A systematic search of observational studies examining the association between PDE5 inhibitor use and melanoma was performed through ClinicalTrials.gov, the Cochrane Library, EMBASE, PubMed, and Web of Science databases, and seven eligible studies were identified. PDE5A gene expression was analyzed with RNA sequencing data from 471 human melanoma samples obtained from The Cancer Genome Atlas. RESULTS: Four studies reported a positive association between PDE5 inhibitor use and melanoma, and three studies found no correlation. RNA sequencing data analysis revealed that under-expression of the PDE5A gene did not impact clinical outcomes in melanoma. CONCLUSIONS: There is currently no evidence to suggest that PDE5 inhibition in patients causes increased risk for melanoma. The few observational studies that demonstrated a positive association between PDE5 inhibitor use and melanoma often failed to account for major confounders. Nonetheless, the substantial evidence implicating PDE5 inhibition in the cyclic guanosine monophosphate (cGMP)-mediated melanoma pathway warrants further investigation in the clinical setting.
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spelling pubmed-67043032019-09-04 No Causal Link between Phosphodiesterase Type 5 Inhibition and Melanoma Wang, Jenny Z. Le, Stephanie Alexanian, Claire Boddu, Sucharita Merleev, Alexander Marusina, Alina Maverakis, Emanual World J Mens Health Original Article PURPOSE: To examine the association between phosphodiesterase type 5 (PDE5) inhibitor use and melanoma by 1) conducting a systematic review of observational studies; and 2) determining if low PDE5A gene expression in human melanoma correlated with decreased overall survival. MATERIALS AND METHODS: A systematic search of observational studies examining the association between PDE5 inhibitor use and melanoma was performed through ClinicalTrials.gov, the Cochrane Library, EMBASE, PubMed, and Web of Science databases, and seven eligible studies were identified. PDE5A gene expression was analyzed with RNA sequencing data from 471 human melanoma samples obtained from The Cancer Genome Atlas. RESULTS: Four studies reported a positive association between PDE5 inhibitor use and melanoma, and three studies found no correlation. RNA sequencing data analysis revealed that under-expression of the PDE5A gene did not impact clinical outcomes in melanoma. CONCLUSIONS: There is currently no evidence to suggest that PDE5 inhibition in patients causes increased risk for melanoma. The few observational studies that demonstrated a positive association between PDE5 inhibitor use and melanoma often failed to account for major confounders. Nonetheless, the substantial evidence implicating PDE5 inhibition in the cyclic guanosine monophosphate (cGMP)-mediated melanoma pathway warrants further investigation in the clinical setting. Korean Society for Sexual Medicine and Andrology 2019-09 2018-10-10 /pmc/articles/PMC6704303/ /pubmed/30350485 http://dx.doi.org/10.5534/wjmh.180050 Text en Copyright © 2019 Korean Society for Sexual Medicine and Andrology http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Wang, Jenny Z.
Le, Stephanie
Alexanian, Claire
Boddu, Sucharita
Merleev, Alexander
Marusina, Alina
Maverakis, Emanual
No Causal Link between Phosphodiesterase Type 5 Inhibition and Melanoma
title No Causal Link between Phosphodiesterase Type 5 Inhibition and Melanoma
title_full No Causal Link between Phosphodiesterase Type 5 Inhibition and Melanoma
title_fullStr No Causal Link between Phosphodiesterase Type 5 Inhibition and Melanoma
title_full_unstemmed No Causal Link between Phosphodiesterase Type 5 Inhibition and Melanoma
title_short No Causal Link between Phosphodiesterase Type 5 Inhibition and Melanoma
title_sort no causal link between phosphodiesterase type 5 inhibition and melanoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704303/
https://www.ncbi.nlm.nih.gov/pubmed/30350485
http://dx.doi.org/10.5534/wjmh.180050
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