Colorectal cancer (CRC) is the second most common cause of cancer death, leading to almost 1 million deaths per year. Despite constant progress in surgical and therapeutic protocols, the 5-year survival rate of advanced CRC patients remains extremely poor. Colorectal Cancer Stem Cells (CRC-CSCs) are endowed with unique stemness-related properties responsible for resistance, relapse and metastasis. The development of novel therapeutics able to tackle CSCs while avoiding undesired toxicity is a major need for cancer treatment. Natural products are a large reservoir of unexplored compounds with possible anticancer bioactivity, sustainability, and safety. The family of meroterpenoids derived from sponges share interesting bioactive properties. Bioassay-guided frac-tionation of a meroterpenoids extract led to the isolation of three compounds, all cytotoxic against several cancer cell lines: Metachromins U, V and W. In this study, we evaluated the anticancer potential of the most active one, Metachromins V (MV), on patient-derived CRC-CSCs. MV strongly impairs CSCs-viability regardless their mutational background and the cytotoxic effect is maintained on therapy-resistant metastatic CSCs. MV affects cell cycle progression, inducing a block in G2 phase in all the cell lines tested and more pronouncedly in CRC-CSCs. Moreover, MV triggers an important reorganization of the cytoskeleton and a strong reduction of Rho GTPases expression, impairing CRC-CSCs motility and invasion ability. By Proteomic analysis identified a po-tential molecular target of MV: CCAR1, that regulates apoptosis under chemotherapy treatments and affect beta-catenin pathway. Further studies will be needed to confirm and validate these data in in vivo experimental models
Lucchetti, D., Luongo, F., Colella, F., Gurreri, E., Artemi, G., Desiderio, C., Serra, S., Giuliante, F., De Maria Marchiano, R., Sgambato, A., Vitali, A., Fiori, M. E., Exploiting bioactive natural products of marine origin: Evaluation of the meroterpenoid metachromin V as a novel potential therapeutic drug for colorectal cancer, <<BIOMEDICINE & PHARMACOTHERAPY>>, 2023; 162 (Giugno): 114679-114690. [doi:10.1016/j.biopha.2023.114679] [https://hdl.handle.net/10807/240374]
Exploiting bioactive natural products of marine origin: Evaluation of the meroterpenoid metachromin V as a novel potential therapeutic drug for colorectal cancer
Lucchetti, DonatellaPrimo
Investigation
;Luongo, FrancescaSecondo
;Colella, Filomena;Gurreri, Enrico;Artemi, Giulia;Desiderio, Claudia;Giuliante, Felice;De Maria Marchiano, Ruggero;Sgambato, Alessandro
;Vitali, AlbertoPenultimo
;Fiori, Micol EleonoraUltimo
2023
Abstract
Colorectal cancer (CRC) is the second most common cause of cancer death, leading to almost 1 million deaths per year. Despite constant progress in surgical and therapeutic protocols, the 5-year survival rate of advanced CRC patients remains extremely poor. Colorectal Cancer Stem Cells (CRC-CSCs) are endowed with unique stemness-related properties responsible for resistance, relapse and metastasis. The development of novel therapeutics able to tackle CSCs while avoiding undesired toxicity is a major need for cancer treatment. Natural products are a large reservoir of unexplored compounds with possible anticancer bioactivity, sustainability, and safety. The family of meroterpenoids derived from sponges share interesting bioactive properties. Bioassay-guided frac-tionation of a meroterpenoids extract led to the isolation of three compounds, all cytotoxic against several cancer cell lines: Metachromins U, V and W. In this study, we evaluated the anticancer potential of the most active one, Metachromins V (MV), on patient-derived CRC-CSCs. MV strongly impairs CSCs-viability regardless their mutational background and the cytotoxic effect is maintained on therapy-resistant metastatic CSCs. MV affects cell cycle progression, inducing a block in G2 phase in all the cell lines tested and more pronouncedly in CRC-CSCs. Moreover, MV triggers an important reorganization of the cytoskeleton and a strong reduction of Rho GTPases expression, impairing CRC-CSCs motility and invasion ability. By Proteomic analysis identified a po-tential molecular target of MV: CCAR1, that regulates apoptosis under chemotherapy treatments and affect beta-catenin pathway. Further studies will be needed to confirm and validate these data in in vivo experimental modelsFile | Dimensione | Formato | |
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