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Radiation-induced erectile dysfunction: Recent advances and future directions
Prostate cancer is one of the most prevalent cancers and the second leading cause of cancer-related deaths in men in the United States. A large number of patients undergo radiation therapy (RT) as a standard care of treatment; however, RT causes erectile dysfunction (radiation-induced erectile dysfu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514009/ https://www.ncbi.nlm.nih.gov/pubmed/28740886 http://dx.doi.org/10.1016/j.adro.2016.05.003 |
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author | Mahmood, Javed Shamah, Aksinija A. Creed, T. Michael Pavlovic, Radmila Matsui, Hotaka Kimura, Masaki Molitoris, Jason Shukla, Hem Jackson, Isabel Vujaskovic, Zeljko |
author_facet | Mahmood, Javed Shamah, Aksinija A. Creed, T. Michael Pavlovic, Radmila Matsui, Hotaka Kimura, Masaki Molitoris, Jason Shukla, Hem Jackson, Isabel Vujaskovic, Zeljko |
author_sort | Mahmood, Javed |
collection | PubMed |
description | Prostate cancer is one of the most prevalent cancers and the second leading cause of cancer-related deaths in men in the United States. A large number of patients undergo radiation therapy (RT) as a standard care of treatment; however, RT causes erectile dysfunction (radiation-induced erectile dysfunction; RiED) because of late side effects after RT that significantly affects quality of life of prostate cancer patients. Within 5 years of RT, approximately 50% of patients could develop RiED. Based on the past and current research findings and number of publications from our group, the precise mechanism of RiED is under exploration in detail. Recent investigations have shown prostate RT induces significant morphologic arterial damage with aberrant alterations in internal pudendal arterial tone. Prostatic RT also reduces motor function in the cavernous nerve which may attribute to axonal degeneration may contributing to RiED. Furthermore, the advances in radiogenomics such as radiation induced somatic mutation identification, copy number variation and genome-wide association studies has significantly facilitated identification of biomarkers that could be used to monitoring radiation-induced late toxicity and damage to the nerves; thus, genomic- and proteomic-based biomarkers could greatly improve treatment and minimize arterial tissue and nerve damage. Further, advanced technologies such as proton beam therapy that precisely target tumor and significantly reduce off-target damage to vital organs and healthy tissues. In this review, we summarize recent advances in RiED research and novel treatment modalities for RiED. We also discuss the possible molecular mechanism involved in the development of RiED in prostate cancer patients. Further, we discuss various readily available methods as well as novel strategies such as stem cell therapies, shockwave therapy, nerve grafting with tissue engineering, and nutritional supplementations might be used to mitigate or cure sexual dysfunction following radiation treatment. |
format | Online Article Text |
id | pubmed-5514009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-55140092017-07-24 Radiation-induced erectile dysfunction: Recent advances and future directions Mahmood, Javed Shamah, Aksinija A. Creed, T. Michael Pavlovic, Radmila Matsui, Hotaka Kimura, Masaki Molitoris, Jason Shukla, Hem Jackson, Isabel Vujaskovic, Zeljko Adv Radiat Oncol Scientific Article Prostate cancer is one of the most prevalent cancers and the second leading cause of cancer-related deaths in men in the United States. A large number of patients undergo radiation therapy (RT) as a standard care of treatment; however, RT causes erectile dysfunction (radiation-induced erectile dysfunction; RiED) because of late side effects after RT that significantly affects quality of life of prostate cancer patients. Within 5 years of RT, approximately 50% of patients could develop RiED. Based on the past and current research findings and number of publications from our group, the precise mechanism of RiED is under exploration in detail. Recent investigations have shown prostate RT induces significant morphologic arterial damage with aberrant alterations in internal pudendal arterial tone. Prostatic RT also reduces motor function in the cavernous nerve which may attribute to axonal degeneration may contributing to RiED. Furthermore, the advances in radiogenomics such as radiation induced somatic mutation identification, copy number variation and genome-wide association studies has significantly facilitated identification of biomarkers that could be used to monitoring radiation-induced late toxicity and damage to the nerves; thus, genomic- and proteomic-based biomarkers could greatly improve treatment and minimize arterial tissue and nerve damage. Further, advanced technologies such as proton beam therapy that precisely target tumor and significantly reduce off-target damage to vital organs and healthy tissues. In this review, we summarize recent advances in RiED research and novel treatment modalities for RiED. We also discuss the possible molecular mechanism involved in the development of RiED in prostate cancer patients. Further, we discuss various readily available methods as well as novel strategies such as stem cell therapies, shockwave therapy, nerve grafting with tissue engineering, and nutritional supplementations might be used to mitigate or cure sexual dysfunction following radiation treatment. Elsevier 2016-06-03 /pmc/articles/PMC5514009/ /pubmed/28740886 http://dx.doi.org/10.1016/j.adro.2016.05.003 Text en © 2016 The Authors on behalf of the American Society for Radiation Oncology http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Scientific Article Mahmood, Javed Shamah, Aksinija A. Creed, T. Michael Pavlovic, Radmila Matsui, Hotaka Kimura, Masaki Molitoris, Jason Shukla, Hem Jackson, Isabel Vujaskovic, Zeljko Radiation-induced erectile dysfunction: Recent advances and future directions |
title | Radiation-induced erectile dysfunction: Recent advances and future directions |
title_full | Radiation-induced erectile dysfunction: Recent advances and future directions |
title_fullStr | Radiation-induced erectile dysfunction: Recent advances and future directions |
title_full_unstemmed | Radiation-induced erectile dysfunction: Recent advances and future directions |
title_short | Radiation-induced erectile dysfunction: Recent advances and future directions |
title_sort | radiation-induced erectile dysfunction: recent advances and future directions |
topic | Scientific Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514009/ https://www.ncbi.nlm.nih.gov/pubmed/28740886 http://dx.doi.org/10.1016/j.adro.2016.05.003 |
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