Advancing the systematics of Araneae: ultraconserved elements phylogenomics demonstrates the non-monophyly of Miturgidae Simon, 1886 and supports the Familial Rank of Systariidae Deeleman-Reinhold, 2001

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  Advancing the systematics of Araneae: ultraconserved elements phylogenomics demonstrates the non-monophyly of Miturgidae Simon, 1886 and supports the Familial Rank of Systariidae Deeleman-Reinhold, 2001 Abstract The systematic status of the family Miturgidae Simon, 1886 and related subfamilies has long been problematic, primarily due to challenges in interpreting morphological characters and limited molecular sampling. In this study, we reconstruct the phylogeny of Miturgidae using ultraconserved elements and estimate its divergence time. Our results suggest that Systariinae does not belong to Miturgidae, but rather is sister to all other families of the Dionycha B clade. Consequently, we elevate it to family rank as Systariidae Deeleman-Reinhold, 2001 and discuss its morphological synapomorphies. Furthermore, our analyses place Miturgidae as the sister clade to Viridasiidae + Selenopidae under multiple phylogenetic methods. Divergence time estimates indicate an ancient origin of...

Cantharidin: a double-edged sword in medicine and toxicology

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Cantharidin: a double-edged sword in medicine and toxicology

Cantharidin (CTD), a natural terpenoid toxin secreted by blister beetles, acts as a potent inhibitor of protein phosphatase. As the principal active component of Mylabris, a traditional Chinese medicine, CTD has attracted considerable interest due to its dual properties, combining potent anti-tumor activity with significant toxicity. Contemporary pharmacological research demonstrates that CTD inhibits the growth and proliferation of diverse cancer cells lines. It exhibits antibacterial and antiparasitic properties, and demonstrates pesticidal activity in agricultural applications. Despite these benefits, CTD exhibits a prominent double-edged profile, marked by severe toxic effects, including cardiotoxicity, nephrotoxicity, gastrointestinal toxicity, and reproductive toxicity. Our prior research has identified the heart and liver as primary targets of CTD’s acute toxicity, where it induces apoptosis and necrosis of cardiomyocytes and hepatocytes. Recent efforts to mitigate its toxicity while preserving efficacy have focused on the structural modifications of CTD and the development of its derivatives. Additionally, CTD has been demonstrated to enhance anti-tumor efficacy when combined with other drugs, particularly against certain drug-resistant tumors. This review comprehensively evaluates CTD’s pharmacology and toxicology, synthesizes pertinent toxicological data, and explores strategies for toxicity reduction to guide future research.

Zhang, J., Tian, T., Li, C., Liu, Y., Wang, Y., Liu, L., Liu, L., & Yao, Y. (2025). Cantharidin: A double-edged sword in medicine and toxicology. Frontiers in Pharmacology, 16, 1644186. https://doi.org/10.3389/fphar.2025.1644186