Analysis of Cembrane-Type Diterpenoids from Cultured Soft Coral Sclerophytum flexibile for Inhibition of TGF-β-Induced IL-6 Secretion in Inflammation-Associated Cancer
Year: 2025
Type: article
Abstract: Cembrane-type diterpenoids (cembranoids), natural compounds derived from soft coral Sclerophytum flexibile, exhibit diverse biological activities including anti-inflammatory, anti-cancer, and anti-viral effects. Our previous research demonstrated that Sinulariolide, a member of this group, effectively inhibits TGF-β-induced IL-6 secretion, thereby suppressing inflammation-associated cancer development. Building on these findings, the present study employs a structure-activity relationship (SAR) approach to compare the anti-inflammatory properties of various cembranoids extracted from cultured soft coral Sclerophytum flexibile—a sustainable and environmentally friendly source that offers a consistent supply for research and therapeutic development. By isolating multiple cembrane-type analogs and analyzing their structural differences, we identified key chemical features that enhance their ability to interfere with TGF-β signaling and subsequent IL-6 production. The SAR analysis revealed distinct variations in anti-inflammatory efficacy among the tested compounds, pinpointing structural motifs crucial for inhibiting TGF-β-induced IL-6 secretion. These insights deepen our understanding of the molecular basis behind the anti-inflammatory action of cembranoids and guide the optimization of these compounds for potential therapeutic use.
Institutions: Tri-Service General Hospital, National Sun Yat-sen University, Zuoying Armed Forces General Hospital, Kaohsiung Armed Forces General Hospital, National Defense Medical Center, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung Medical University, National Museum of Marine Biology and Aquarium, National Dong Hwa University
Language: English
Subfield: Biotechnology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,499
Award: G6738444131
OpenAlex ID: W4416504012
