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Unlocking the Therapeutic Potential of Algae-Derived Compounds in Hematological Malignancies

Articolo
Data di Pubblicazione:
2025
Abstract:
Algae are a rich source of bioactive compounds that have a wide range of beneficial effects on human health and can show significant potential in the treatment of hematological malignancies such as leukemia, lymphoma, and multiple myeloma. These diseases often pose a therapeutic challenge despite recent advances in treatment (e.g., the use of immunomodulatory drugs, proteasome inhibitors, CD38 monoclonal antibodies, stem cell transplant, and targeted therapy). A considerable number of patients experience relapses or resistance to the applied therapies. Algal compounds, alone or in combination with chemotherapy or other more advanced therapies, have exhibited antitumor and immunomodulatory effects in preclinical studies that may improve disease outcomes. These include the ability to induce apoptosis, inhibit tumor growth, and improve immune responses. However, most of these studies are conducted in vitro, often without in vivo validation or clinical trials. This paper summarizes the current evidence on the in vitro effects of algae extracts and isolated compounds on leukemia, lymphoma, and myeloma cell lines. In addition, we address the current advances in the application of algae-derived compounds as targeted drug carriers and their synergistic potential against hematologic malignancies.
Tipologia CRIS:
03B-Review in Rivista / Rassegna della Lett. in Riv. / Nota Critica
Keywords:
algae; antitumor; leukemia; lymphoma; multiple myeloma; natural compounds
Elenco autori:
Vujović, Tamara; Paradžik, Tina; Babić Brčić, Sanja; Piva, Roberto
Autori di Ateneo:
PIVA Roberto
Link alla scheda completa:
https://iris.unito.it/handle/2318/2078479
Link al Full Text:
https://iris.unito.it/retrieve/handle/2318/2078479/1893961/cancers-17-00318.pdf
Pubblicato in:
CANCERS
Journal
Progetto:
Exploiting synthetic lethal interactions to improve the therapeutic efficacy of proteasome inhibitors – ultima annualità AIRC IG 21585
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