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Brown-Algae Derived Therapies for Pancreatic Cancer, a Highly Fatal Disease

Discovering ocean-derived compounds as potential disruptors of cancer progression and catalysts for future therapeutic advances

Pancreatic cancer remains one the most lethal malignancies, characterized by late detection and limited treatment responsiveness. In recent years, naturally occurring compounds from marine organisms have been investigated as potential sources of novel therapeutic agents. Among these, bioactive substances from brown algae have attracted particular scientific interest.


Brown algae synthesizes a diverse array of chemical compounds with biological activity, many of which do not appear in terrestrial plants. This unique biochemical profile has prompted research into their potential anticancer properties, including how cancer cells grow, multiply, or respond to treatment. Two classes of compounds,  fucoidan and phlorotannins, have been the primary focus of current investigations due to their demonstrated effects on cellular processes relevant to pancreatic cancer progression.


Fucoidan: A Multifacted Marine Sugar

Fucoidan is a sulfated polysaccharide, meaning it consists of long chains of sugar molecules that carry sulfate groups. These structural features enable interactions with various cellular pathways:

- Inhibition of tumor cell proliferation: Fucoidan can interfere with growth-promoting signals caused by cancer cells.

- Induction of apoptosis: It appears capable of activating programmed cell death, a controlled mechanism through which damaged or abnormal cells are eliminated.

- Modulation of immune responses: Fucoidan may enhance the body’s ability to detect and respond to malignant cells.

- Reduction of metastatic potential: Evidence suggests it can disrupt processes that allow cancer cells to migrate and colonize distant tissues.


Phlorotannins: Polyphenolic Compounds With Targeted Bioactivity

Phlorotannins are a group of polyphenols, a category of plant-derived molecules known for antioxidant properties. Their relevance in pancreatic cancer research stems from their ability to influence several pathways associated with tumor progression:

- Antioxidant and anti-inflammatory effects: These properties may counter cellular stress and inflammatory environments that support tumor growth.

- Inhibition of epithelial-mesenchymal transition (EMT): EMT is a process by which cancer cells acquire greater mobility and invasiveness; phlorotannins may help prevent this transition.

- Suppression of oncogenic signaling: They appear capable of interrupting molecular pathways that drive uncontrolled cell growth.


Current research extends beyond isolated compound effects and includes exploration of combination treatments. Preliminary findings suggest that fucoidan and phlorotannins may enhance the efficacy of conventional chemotherapeutic agents, potentially through synergistic interactions.


Additionally, efforts are underway to improve bioavailability, a term describing how effectively a substance is absorbed and utilized by the body. Nano-delivery systems, engineered particles designed to transport therapeutic compounds more efficiently, are being evaluated to increase the stability and uptake of algae-derived molecules.


The growing body of evidence highlights an exciting possibility: that substances found in marine algae may one day serve as adjunct therapies, supporting conventional treatments and offering patients new hope against one of the deadliest cancers.


Bioactive compounds from marine algae in pancreatic cancer therapy: mechanistic insights into fucoidan and phlorotannins: a review

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