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Sirtuin inhibition by plumbagin connects protein acetylation to cell division

Title: Sirtuin inhibition by plumbagin connects protein acetylation to cell division
Authors: Sirri, Valentina; Vidal, Antoine; Roussel, Pascal
Contributors: Unité de Biologie Fonctionnelle et Adaptative (BFA (UMR_8251 / U1133)); Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité)
Source: ISSN: 0021-9533.
Publisher Information: CCSD; Company of Biologists
Publication Year: 2026
Collection: Inserm: HAL (Institut national de la santé et de la recherche médicale)
Subject Terms: naphthoquinone; cell cycle; mitotic spindle; sirtuin; HDAC; [SDV.BC.BC]Life Sciences [q-bio]/Cellular Biology/Subcellular Processes [q-bio.SC]; [SDV.SP.PHARMA]Life Sciences [q-bio]/Pharmaceutical sciences/Pharmacology
Description: International audience ; Naphthoquinones interfere with biological systems and exhibit pharmaceutical properties. As an electrophile, the naphthoquinone plumbagin may react with nucleophiles, mainly thiols, and form covalent adducts. Here, we have further characterized the effects of plumbagin in HeLa cells. First, we demonstrate that plumbagin interferes with mitosis by affecting the mitotic spindle formation without preventing exit from mitosis. This plumbagin-induced delay in cell division was reproduced by class III histone deacetylase (HDAC) inhibitors but not by the class I, II and IV pan-HDAC inhibitor trichostatin A; therefore, it most likely involves sirtuins. Second, we establish that, in addition to blocking cell division, plumbagin induces protein hyperacetylation in a sulfhydryl arylation-dependent manner. Finally, in a manner consistent with the plumbagin-dependent inhibition of sirtuin 2 (SIRT2), we show that plumbagin interferes with the centrosomal localization of SIRT2 and induces increased acetylation of α-tubulin, a SIRT2 target. Inhibition of sirtuin activity induces hyperacetylation of proteins such as TPX2 and its delocalization, and consequently interferes with mitotic spindle formation and cell division. Since plumbagin most likely inhibits SIRT2, which is known to modulate several proteins involved in different pathological processes, we propose that it could be a promising therapeutic agent.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1242/jcs.264052
Availability: https://hal.science/hal-05653485; https://hal.science/hal-05653485v1/document; https://hal.science/hal-05653485v1/file/Sirri%20et%20al.%202026.pdf; https://doi.org/10.1242/jcs.264052
Rights: https://creativecommons.org/licenses/by/4.0/ ; info:eu-repo/semantics/OpenAccess
Accession Number: edsbas.43ED0D63
Database: BASE