TY - JOUR
T1 - Anti-cancer activity of Ajwa dates extract (Phoenix Dactylifera L.) through analysis of MCL-1 levels, EGFR, and p53 expressions on apoptosis in human prostate cancer cell lines PC3
T2 - an in vitro study
AU - Azis, Abdul
AU - Islam, Andi Asadul
AU - Rasyid, Haerani
AU - Yustisia, Ika
AU - Hakim, Lukman
AU - Bakri, Syakib
AU - Bukhari, Agussalim
AU - Zainuddin, Andi Alfian
PY - 2025/9/30
Y1 - 2025/9/30
N2 - INTRODUCTION & OBJECTIVES: Prostate cancer is recognized as a global burden disease related to malignancy in men. Several fruit and plant-based supplementation have been studied to evaluate their utility for the management of prostate cancer. Ajwa dates (Phoenix Dactylifera L.) have been known to contain various beneficial compounds, which makes them a potential anti-cancer therapy. The aim of this study was to assess the effect of Ajwa dates on prostate cancer cell lines PC3 through analysis of MCL-1 levels, EGFR, and p53 expressions on apoptosis. MATERIALS & METHODS: This study was an experimental in vitro study with post-test-only control design. Groups were divided into four: control group, abiraterone group, Ajwa dates group, and combination group (abiraterone and Ajwa dates). Viability test was conducted using the CCK-8 method to determine the inhibitory concentration (IC50) of Ajwa dates after a 72-hour incubation period of PC3 cells. The MCL-1 levels were rated using ELISA, while EGFR and p53 expressions were analyzed using immunofluorescence microscopic staining. Apoptosis was measured using fluorescence-activated cell sorting (FACS). SPSS version 25 and R-studio were used for statistical analysis. RESULTS: This study found the IC50 for Ajwa dates was 913.3 μg/ml. Our data indicated that Ajwa dates decrease the MCL-1 levels, EGFR and p53 expression and also induced apoptosis compared to control. Furthermore, these effects became more evident when combined with abiraterone. CONCLUSIONS: This study demonstrates the potential of Ajwa dates as a complementary therapy for prostate cancer, but further research is still needed before clinical testing is carried out.
AB - INTRODUCTION & OBJECTIVES: Prostate cancer is recognized as a global burden disease related to malignancy in men. Several fruit and plant-based supplementation have been studied to evaluate their utility for the management of prostate cancer. Ajwa dates (Phoenix Dactylifera L.) have been known to contain various beneficial compounds, which makes them a potential anti-cancer therapy. The aim of this study was to assess the effect of Ajwa dates on prostate cancer cell lines PC3 through analysis of MCL-1 levels, EGFR, and p53 expressions on apoptosis. MATERIALS & METHODS: This study was an experimental in vitro study with post-test-only control design. Groups were divided into four: control group, abiraterone group, Ajwa dates group, and combination group (abiraterone and Ajwa dates). Viability test was conducted using the CCK-8 method to determine the inhibitory concentration (IC50) of Ajwa dates after a 72-hour incubation period of PC3 cells. The MCL-1 levels were rated using ELISA, while EGFR and p53 expressions were analyzed using immunofluorescence microscopic staining. Apoptosis was measured using fluorescence-activated cell sorting (FACS). SPSS version 25 and R-studio were used for statistical analysis. RESULTS: This study found the IC50 for Ajwa dates was 913.3 μg/ml. Our data indicated that Ajwa dates decrease the MCL-1 levels, EGFR and p53 expression and also induced apoptosis compared to control. Furthermore, these effects became more evident when combined with abiraterone. CONCLUSIONS: This study demonstrates the potential of Ajwa dates as a complementary therapy for prostate cancer, but further research is still needed before clinical testing is carried out.
UR - https://www.scopus.com/pages/publications/105017652373
U2 - 10.4081/aiua.2025.14027
DO - 10.4081/aiua.2025.14027
M3 - Article
C2 - 40824063
AN - SCOPUS:105017652373
SN - 1124-3562
VL - 97
SP - 14027
JO - Archivio Italiano di Urologia e Andrologia
JF - Archivio Italiano di Urologia e Andrologia
IS - 3
ER -