The efficacy of natural bioactive compounds against prostate cancer: Molecular targets and synergistic activities.
Md Abdur Rashid MiaDipta DeyMusfiqur Rahman SakibMd Yeaman BiswasAbdullah Al Shamsh ProttayNiloy PaulFahmida Hoque RimtiYusuf AbdullahPartha BiswasMd IftehimulPriyanka PaulChandan SarkarHeba A S El-NasharMohamed El-ShazlyMuhammad Torequl IslamPublished in: Phytotherapy research : PTR (2023)
Globally, prostate cancer (PCa) is regarded as a challenging health issue, and the number of PCa patients continues to rise despite the availability of effective treatments in recent decades. The current therapy with chemotherapeutic drugs has been largely ineffective due to multidrug resistance and the conventional treatment has restricted drug accessibility to malignant tissues, necessitating a higher dosage resulting in increased cytotoxicity. Plant-derived bioactive compounds have recently attracted a great deal of attention in the field of PCa treatment due to their potent effects on several molecular targets and synergistic effects with anti-PCa drugs. This review emphasizes the molecular mechanism of phytochemicals on PCa cells, the synergistic effects of compound-drug interactions, and stem cell targeting for PCa treatment. Some potential compounds, such as curcumin, phenethyl-isothiocyanate, fisetin, baicalein, berberine, lutein, and many others, exert an anti-PCa effect via inhibiting proliferation, metastasis, cell cycle progression, and normal apoptosis pathways. In addition, multiple studies have demonstrated that the isolated natural compounds: d-limonene, paeonol, lanreotide, artesunate, and bicalutamide have potential synergistic effects. Further, a significant number of natural compounds effectively target PCa stem cells. However, further high-quality studies are needed to firmly establish the clinical efficacy of these phytochemicals against PCa.
Keyphrases
- stem cells
- prostate cancer
- cell cycle
- cancer therapy
- oxidative stress
- public health
- end stage renal disease
- signaling pathway
- cell cycle arrest
- gene expression
- emergency department
- cell proliferation
- chronic kidney disease
- newly diagnosed
- ejection fraction
- induced apoptosis
- endoplasmic reticulum stress
- working memory
- risk assessment
- combination therapy
- single molecule
- prognostic factors
- social media
- patient reported