Anti-cancer potential of a new derivative of Caffeic Acid Phenethyl Ester targeting the centrosomeVise andre og tillknytning
2025 (engelsk)Inngår i: Redox Biology, E-ISSN 2213-2317, Vol. 81, artikkel-id 103582
Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]
Anaplastic Large Cell Lymphoma (ALCL) is an aggressive T-cell lymphoma affecting children and young adults. About 30% of patients develop therapy resistance therefore new precision medicine drugs are highly warranted. Multiple rounds of structure-activity optimization of Caffeic Acid Phenethyl Ester have resulted in CM14. CM14 causes upregulation of genes involved in oxidative stress response and downregulation of DNA replication genes leading to G2/M arrest and subsequent apoptosis induction. In accordance with this, an unbiased proteomics approach, confocal microscopy and molecular modeling showed that TUBGCP2, member of the centrosomal γ-TuRC complex, is a direct interaction partner of CM14. CM14 overcomes ALK inhibitor resistance in ALCL and is also active in T-cell Acute Lymphoblastic Leukemia and Acute Myeloid Leukemia. Interestingly, CM14 also induced cell death in docetaxel-resistant prostate cancer cells thus suggesting an unexpected role in solid cancers. Thus, we synthesized and thoroughly characterized a novel TUBGCP2 targeting drug that is active in ALCL but has also potential for other malignancies.
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Elsevier, 2025. Vol. 81, artikkel-id 103582
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Identifikatorer
URN: urn:nbn:se:umu:diva-237661DOI: 10.1016/j.redox.2025.103582ISI: 001446494100001PubMedID: 40073758Scopus ID: 2-s2.0-86000586796OAI: oai:DiVA.org:umu-237661DiVA, id: diva2:1954019
2025-04-232025-04-232025-04-23bibliografisk kontrollert