1Department of Anti-Aging and Regenerative Medicine, College of Integrative Medicine, Dhurakij Pundit University, Thailand
2Department of Otorhinolaryngology, Head and Neck Surgery, Samitivej Thonburi Hospital, Thailand
3Department of Emergency Medicine, Navavej International Hospital, Thailand
4Faculty of Pharmacy, Chiangmai University, Thailand
*Corresponding author:Wanlapa Sakritthichai, College of Integrative Medicine, Dhurakij Pundit University, 110/1-4 Prachachuen Rd, Laksi, Bangkok 10210, Thailand.
Submission: June 4, 2025;Published: June 16, 2025
Volume8 Issue 2 June 16, 2025
Background: Prostate cancer is a major cause of cancer-related death in men globally. Lycopene, a
carotenoid found in tomatoes and related products, has strong antioxidant properties and may reduce
prostate cancer risk.
Methods: A systematic review and meta-analysis were conducted using PubMed,
Scopus, Cochrane Library and ScienceDirect up to September 2024. Twenty-three observational studies
involving 414,128 participants and 33,552 prostate cancer cases. Pooled odds ratios (ORs) and 95%
confidence intervals (CIs) were calculated using random-and fixed-effects models.
Results: High dietary lycopene intake was significantly associated with reduced prostate cancer risk
(OR=0.91, 95% CI: 0.84-0.99, P=0.03), especially at >10 mg/day. Lycopene intake also reduced advanced
prostate cancer risk (OR=0.88, 95% CI: 0.78-0.99, P=0.04), notably at >15 mg/day. Serum lycopene levels
were associated with prostate cancer risk (OR = 0.83, 95% CI: 0.73-0.96, P = 0.009). Greater risk reduction
was seen in studies with >10 years follow-up (OR=0.92, P = 0.003).
Conclusion: Higher lycopene intake and serum levels are associated with reduced prostate cancer risk.
Notably, lycopene intake also appears to decrease the risk of advanced prostate cancer. These findings
highlight its potential as a preventive dietary factor.
Keywords:Lycopene; Prostate cancer; Meta-analysis; Antioxidant
Abbreviations: CI: Confidence Interval; OR: Odds Ratio; PCA: Prostate Cancer; PRISMA: Preferred Reporting Items for Systematic Reviews and Meta-Analyses; REVMAN: Review Manager; NOS: Newcastle- Ottawa Scale; PCA: Prostate Cancer; NCC: Nested Case-Control; CC: Case-Control; FFQ: Food Frequency Questionnaire; Q: Quantile; FHPC: Family History of Prostate Cancer; BMI: Body Mass Index; NA: Not Applicable; CLUE I: Give us a CLUE to Cancer Study I; CLUE II: Give us a CLUE to Cancer Study II; NSAIDS: Non-Steroidal Anti-Inflammatory Drugs; RCTs: Randomized Controlled Trials