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Updated: May 13, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Caffeic Acid phenethyl ester as a potential treatment for advanced prostate cancer targeting akt signaling
Hui-Ping Lin1, Ching-Yu Lin, Chun-Chieh Liu
1Institute of Cellular and System Medicine, National Health Research Institutes, Miaoli 35053, Taiwan. cpchuu@nhri.org.tw.
Abstract:
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.
Insights
Caffeic acid phenethyl ester (CAPE), an antioxidant, shows promise for treating advanced prostate cancer by inhibiting the PI3K/Akt pathway, which is often dysregulated in recurrent tumors.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Prostate cancer is a leading global cancer, with metastatic disease often becoming castration-resistant despite androgen ablation therapy.
- Recurrent prostate tumors frequently exhibit PTEN mutations, leading to aberrant PI3K/Akt signaling, a key driver of cancer progression.
- Current treatments for metastatic hormone-refractory prostate cancer, including chemotherapy, offer limited survival benefits.
Purpose of the Study:
- To review the potential of Caffeic acid phenethyl ester (CAPE) as a therapeutic agent for advanced prostate cancer.
- To explore CAPE's mechanism of action, specifically its role in inhibiting the PI3K/Akt signaling pathway.
- To highlight CAPE as a potential treatment targeting Akt signaling in recurrent prostate tumors.
Main Methods:
- Literature review of studies on prostate cancer, androgen ablation therapy, and PI3K/Akt signaling.
- Analysis of research on Caffeic acid phenethyl ester (CAPE), its properties, and its effects on cancer cells.
- Examination of studies investigating CAPE's impact on Akt signaling and tumor growth in prostate cancer models.
Main Results:
- The PI3K/Akt signaling pathway is frequently activated in advanced prostate cancer, particularly in castration-resistant tumors.
- Caffeic acid phenethyl ester (CAPE), a natural antioxidant and NF-κB inhibitor, has demonstrated tumor growth suppression in prostate cancer cells.
- CAPE treatment has been shown to inhibit Akt signaling in human prostate cancer cells.
Conclusions:
- Inhibition of the PI3K/Akt pathway presents a viable therapeutic strategy for advanced prostate cancer.
- Caffeic acid phenethyl ester (CAPE) exhibits potential as a novel treatment for advanced prostate cancer by targeting the Akt signaling pathway.
- Further research into CAPE's efficacy and safety is warranted for its clinical application in prostate cancer treatment.
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