Curcumin & Prostate Cancer: Mechanisms & Nanotherapy – BMC Cancer

by Grace Chen

Curcumin Shows Promise as Multi-Targeted Therapy for Prostate Cancer, New Review Finds

A systematic review published in early 2025 reveals compelling preclinical evidence supporting curcuminS potential as a multifaceted treatment for prostate cancer (PCa), acting on numerous molecular pathways and benefiting from innovative delivery strategies. While challenges remain in translating these findings to clinical practice, researchers are optimistic about the future of curcumin-based interventions.

Curcumin, a naturally occurring dietary polyphenol derived from the spice Curcuma longa, has long been recognized for its broad range of biological activities. This latest analysis distinguishes itself by focusing exclusively on prostate cancer, systematically evaluating both the underlying molecular mechanisms and the emerging role of nanoformulation techniques. According to the review,this approach provides a more clinically relevant and up-to-date perspective than previous,broader examinations of curcumin’s anticancer properties.

Targeting Key pathways in Prostate Cancer

A central mechanism through which curcumin exerts its antitumor effects is the inhibition of the PI3K/Akt/mTOR axis, a critical signaling pathway frequently disrupted in prostate tumorigenesis, especially in cases lacking the PTEN tumor suppressor gene. Researchers found that nanoparticle-formulated curcumin (Theracurmin) effectively reduced PI3K/Akt signaling in early-stage PCa, suggesting a potential role in cancer prevention rather than simply killing existing cancer cells.

However, the review also highlights the power of combination therapies. Functionalized nanoparticles delivering both curcumin and the chemotherapy drug cabazitaxel demonstrated a synergistic effect, suppressing the PI3K/Akt and NF-κB pathways while simultaneously enhancing apoptosis – programmed cell death – and tumor regression in laboratory models. “This demonstrates the potential of rationally combining curcumin with existing treatments to achieve a more potent anticancer effect,” one analyst noted.

Modulating Androgen Receptor Signaling

Curcumin’s ability to modulate the androgen receptor (AR) signaling pathway is another key aspect of its relevance in prostate cancer, impacting both hormone-sensitive and castration-resistant forms of the disease. A curcumin analog, H10, was shown to selectively inhibit the enzyme 17β-HSD3, reducing testosterone levels within tumors without affecting other enzymes in the pathway. This targeted approach led to AR suppression and reduced tumor growth. Furthermore, combining curcumin with dutasteride considerably reduced PSA expression, induced DNA damage, and enhanced apoptosis, reinforcing its potential as an addition to standard androgen deprivation therapy.

Inducing Multiple Forms of Cell Death

The induction of apoptosis was consistently observed across various models.Mechanistic studies revealed activation of both intrinsic (Bax, caspase-3) and extrinsic (DR4/DR5) apoptotic pathways, frequently enough accompanied by mitochondrial dysfunction and the generation of reactive oxygen species (ROS). interestingly, researchers discovered that in prostate cancer cells adapted to the acidic surroundings of tumors, curcumin triggered both apoptosis and necroptosis – a rare and highly cytotoxic form of cell death – through oxidative stress and ATP depletion.This dual-mode cell death strategy could possibly overcome resistance in advanced PCa.

Beyond Cell Death: Inhibiting Metastasis

Beyond directly killing cancer cells, curcumin also demonstrated the ability to inhibit migration, invasion, and angiogenesis – the formation of new blood vessels that feed tumors. This was achieved by modulating EMT markers (E-cadherin↑, ZEB1↓, vimentin↓) and angiogenic regulators (CD31↓). These effects are particularly crucial in aggressive, metastatic PCa models like

However, several challenges must be addressed before curcumin can be widely adopted as a PCa treatment. These include poor bioavailability, rapid metabolism, and limited absorption. Furthermore, issues related to formulation, including potential toxicity, manufacturing difficulties, and batch-to-batch variability, also require attention. Future research should prioritize standardized dosing protocols, pharmacokinetic and toxicological profiling, biomarker-driven patient stratification, and exploration of curcumin as an adjuvant to immunotherapy and radiotherapy.

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