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Majusculamide-o, a simplified marine natural product analog, exhibits potent and specific cancer cell cytotoxicity

Title: Majusculamide-o, a simplified marine natural product analog, exhibits potent and specific cancer cell cytotoxicity
Authors: Niklas Alexander Wahl; Naiara Lebrón-Acosta; Michelle Pérez-Cuevas; Angel Hernandez-Mejias; Dmitry Leshchiner; Frederick A. Valeriote; Eduardo J. E. Caro-Diaz; Sachi Horibata
Source: Scientific Reports, Vol 15, Iss 1, Pp 1-14 (2025)
Publisher Information: Nature Portfolio
Publication Year: 2025
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: Natural compounds; Cancers; Anti-cancer drugs; Medicine; Science
Description: Metastatic solid tumors (e.g., ovary, pancreas, liver, lung, and brain) contribute to a high mortality rate in cancer patients with few therapeutically effective anticancer drugs available for their treatment, highlighting the need to develop agents that target solid tumors. Natural products (NPs) derived from cyanobacteria possess potent anticancer activity, yet most are hard to synthesize and modify to improve therapeutic efficacy. Here, we have efficiently synthesized a simplified analog of the marine NP majusculamide D, majusculamide o (maj-o, 1), that has remarkable potency and selective cytotoxicity towards various metastatic cancer cells. We found that maj-o (1) treatment presents potent cytotoxicity in various cancer cell lines of the ovary (OVCAR3), pancreas (PANC1), brain (U251N), and lung (H125) in a dose-dependent manner, with the least cytotoxic effect towards non-metastatic or primary tumors of the liver (HEPG2) and ovary (OVCAR8). 1 significantly alters gene expression signatures with more treatment time and affects pathways associated with PI3K-Akt signaling and the Hippo pathway. Our finding suggests that maj-o has great potential to serve as a lead compound for the development of novel antineoplastics for solid tumors.
Document Type: article in journal/newspaper
Language: English
Relation: https://doi.org/10.1038/s41598-025-23480-3; https://doaj.org/toc/2045-2322; https://doaj.org/article/8b44f4390195495e93f258d2322491dd
DOI: 10.1038/s41598-025-23480-3
Availability: https://doi.org/10.1038/s41598-025-23480-3; https://doaj.org/article/8b44f4390195495e93f258d2322491dd
Accession Number: edsbas.2404C901
Database: BASE