Aug 2026· Medical Oncology· Vol 43· 0 citations· 45 references
Medicine
TL;DR
Findings highlight the novelty of KYNU as a therapeutic target and support the development of KS79356 as a potential treatment strategy for TNBC progression and metastasis.
Butoconazole is repurposed as a novel allosteric inhibitor of glucose-regulated protein 78 (GRP78) for TNBC treatment and represents a promising lead compound for further development as a systemic anti-TNBC agent through formulation optimization.
Yaowen Song, Ziyue Yuan, Zhi-Jia Li et al.· Bioorganic chemistry (Print)· 0 citations
Summary Triple-negative breast cancer (TNBC) lacks effective targeted therapies, and YTHDF proteins are frequently overexpressed in this malignancy, which correlates with adverse prognosis. Through high-throughput drug screening, we identify ellagic acid (EA) as a compound that binds to YTHDF proteins and disrupts thei...
GPX4 is identified as the principal mediator of MLN4924-induced ferroptosis and dual targeting of GPX4 transcription and activity represents a promising therapeutic strategy for GBM, establishing that dual targeting of GPX4 transcription and activity represents a promising therapeutic strategy.
Zhou Jing, Fangyuan Wang, Hao Li et al.· Carcinogenesis· 0 citations
Aliflorin suppresses BC progression by inhibiting the HINT2/NLRP3 signaling pathway, suggesting HINT2 is a viable biomarker and Al a promising therapeutic agent for BC treatment.
Background Non-small cell lung cancer (NSCLC) remains a major cause of cancer-related mortality, and safer combination strategies with improved antitumor efficacy are still needed. Berberine (BBR), a natural isoquinoline alkaloid with multi-target pharmacological activity, and celecoxib (CXB), a selective cyclooxygenas...
Qiang Wang, Chen-Feng Bian, Xin-Yuan She et al.· Frontiers in Pharmacology· 0 citations
A novel METTL3/ELF1/GPX4 axis through which METTL3 promotes TNBC growth by regulating oxidative stress and ferroptosis-related markers is suggested, providing a basis for further investigation of this pathway in the context of TNBC biology and therapeutic development.
Jin-Chen Wang, Wei Wang, Jun-Jie Hu et al.· Asia-Pacific Journal of Clin...· 0 citations
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