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Caffeic Acid Phenethyl Ester as a Potential Treatment for Advanced Prostate Cancer Targeting Akt Signaling

Prostate cancer is the fifth most common cancer overall in the world. Androgen ablation therapy is the primary treatment for metastatic prostate cancer. However, most prostate cancer patients receiving the androgen ablation therapy ultimately develop recurrent castration-resistant tumors within 1–3...

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Autores principales: Lin, Hui-Ping, Lin, Ching-Yu, Liu, Chun-Chieh, Su, Liang-Cheng, Huo, Chieh, Kuo, Ying-Yu, Tseng, Jen-Chih, Hsu, Jong-Ming, Chen, Chi-Kuan, Chuu, Chih-Pin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634405/
https://www.ncbi.nlm.nih.gov/pubmed/23466879
http://dx.doi.org/10.3390/ijms14035264
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author Lin, Hui-Ping
Lin, Ching-Yu
Liu, Chun-Chieh
Su, Liang-Cheng
Huo, Chieh
Kuo, Ying-Yu
Tseng, Jen-Chih
Hsu, Jong-Ming
Chen, Chi-Kuan
Chuu, Chih-Pin
author_facet Lin, Hui-Ping
Lin, Ching-Yu
Liu, Chun-Chieh
Su, Liang-Cheng
Huo, Chieh
Kuo, Ying-Yu
Tseng, Jen-Chih
Hsu, Jong-Ming
Chen, Chi-Kuan
Chuu, Chih-Pin
author_sort Lin, Hui-Ping
collection PubMed
description Prostate cancer is the fifth most common cancer overall in the world. Androgen ablation therapy is the primary treatment for metastatic prostate cancer. However, most prostate cancer patients receiving the androgen ablation therapy ultimately develop recurrent castration-resistant tumors within 1–3 years after treatment. The median overall survival time is 1–2 years after tumor relapse. Chemotherapy shows little effect on prolonging survival for patients with metastatic hormone-refractory prostate cancer. More than 80% of prostate tumors acquire mutation or deletion of tumor suppressor phosphatase and tensin homolog (PTEN), a negative regulator of PI3K/Akt signaling, indicating that inhibition of PI3K/Akt might be a potential therapy for advanced prostate tumors. Caffeic acid phenethyl ester (CAPE) is a strong antioxidant extracted from honeybee hive propolis. CAPE is a well-known NF-κB inhibitor. CAPE has been used in folk medicine as a potent anti-inflammatory agent. Recent studies indicate that CAPE treatment suppresses tumor growth and Akt signaling in human prostate cancer cells. We discuss the potential of using CAPE as a treatment for patients with advanced prostate cancer targeting Akt signaling pathway in this review article.
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spelling pubmed-36344052013-05-02 Caffeic Acid Phenethyl Ester as a Potential Treatment for Advanced Prostate Cancer Targeting Akt Signaling Lin, Hui-Ping Lin, Ching-Yu Liu, Chun-Chieh Su, Liang-Cheng Huo, Chieh Kuo, Ying-Yu Tseng, Jen-Chih Hsu, Jong-Ming Chen, Chi-Kuan Chuu, Chih-Pin Int J Mol Sci Review Prostate cancer is the fifth most common cancer overall in the world. Androgen ablation therapy is the primary treatment for metastatic prostate cancer. However, most prostate cancer patients receiving the androgen ablation therapy ultimately develop recurrent castration-resistant tumors within 1–3 years after treatment. The median overall survival time is 1–2 years after tumor relapse. Chemotherapy shows little effect on prolonging survival for patients with metastatic hormone-refractory prostate cancer. More than 80% of prostate tumors acquire mutation or deletion of tumor suppressor phosphatase and tensin homolog (PTEN), a negative regulator of PI3K/Akt signaling, indicating that inhibition of PI3K/Akt might be a potential therapy for advanced prostate tumors. Caffeic acid phenethyl ester (CAPE) is a strong antioxidant extracted from honeybee hive propolis. CAPE is a well-known NF-κB inhibitor. CAPE has been used in folk medicine as a potent anti-inflammatory agent. Recent studies indicate that CAPE treatment suppresses tumor growth and Akt signaling in human prostate cancer cells. We discuss the potential of using CAPE as a treatment for patients with advanced prostate cancer targeting Akt signaling pathway in this review article. Molecular Diversity Preservation International (MDPI) 2013-03-06 /pmc/articles/PMC3634405/ /pubmed/23466879 http://dx.doi.org/10.3390/ijms14035264 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Lin, Hui-Ping
Lin, Ching-Yu
Liu, Chun-Chieh
Su, Liang-Cheng
Huo, Chieh
Kuo, Ying-Yu
Tseng, Jen-Chih
Hsu, Jong-Ming
Chen, Chi-Kuan
Chuu, Chih-Pin
Caffeic Acid Phenethyl Ester as a Potential Treatment for Advanced Prostate Cancer Targeting Akt Signaling
title Caffeic Acid Phenethyl Ester as a Potential Treatment for Advanced Prostate Cancer Targeting Akt Signaling
title_full Caffeic Acid Phenethyl Ester as a Potential Treatment for Advanced Prostate Cancer Targeting Akt Signaling
title_fullStr Caffeic Acid Phenethyl Ester as a Potential Treatment for Advanced Prostate Cancer Targeting Akt Signaling
title_full_unstemmed Caffeic Acid Phenethyl Ester as a Potential Treatment for Advanced Prostate Cancer Targeting Akt Signaling
title_short Caffeic Acid Phenethyl Ester as a Potential Treatment for Advanced Prostate Cancer Targeting Akt Signaling
title_sort caffeic acid phenethyl ester as a potential treatment for advanced prostate cancer targeting akt signaling
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634405/
https://www.ncbi.nlm.nih.gov/pubmed/23466879
http://dx.doi.org/10.3390/ijms14035264
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