Dimethyl itaconate selectively targets inflammatory and metabolic pathways in chronic lymphocytic leukemia.


Journal

European journal of immunology
ISSN: 1521-4141
Titre abrégé: Eur J Immunol
Pays: Germany
ID NLM: 1273201

Informations de publication

Date de publication:
10 2023
Historique:
revised: 30 06 2023
received: 04 02 2023
accepted: 07 08 2023
medline: 23 10 2023
pubmed: 10 8 2023
entrez: 10 8 2023
Statut: ppublish

Résumé

Chronic lymphocytic leukemia (CLL) co-evolves with its own microenvironment where inflammatory stimuli including toll-like receptors (TLR) signaling can protect CLL cells from spontaneous and drug-induced apoptosis by upregulating IκBζ, an atypical co-transcription factor. To dissect IκBζ-centered signaling pathways, we performed a gene expression profile of primary leukemic cells expressing either high or low levels of IκBζ after stimulation, highlighting that IκBζ is not only an inflammatory gene but it may control metabolic rewiring of malignant cells thus pointing to a novel potential opportunity for therapy. We exploited the capacity of the dimethyl itaconate (DI), an anti-inflammatory electrophilic synthetic derivative of the metabolite Itaconate, to target IκBζ. CLL cells, murine leukemic splenocytes, and leukocytes from healthy donors were treated in vitro with DI that abolished metabolic activation and reduced cell viability of leukemic cells only, even in the presence of robust TLR prestimulation. RNA sequencing highlighted that in addition to the expected electrophilic stress signature observed after DI treatment, novel pathways emerged including the downregulation of distinct MHC class II complex genes. In conclusion, DI not only abrogated the proinflammatory effects of TLR stimulation but also targeted a specific metabolic vulnerability in CLL cells.

Identifiants

pubmed: 37561992
doi: 10.1002/eji.202350418
doi:

Substances chimiques

dimethyl itaconate 11JIB0YI93
Toll-Like Receptors 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2350418

Informations de copyright

© 2023 The Authors. European Journal of Immunology published by Wiley-VCH GmbH.

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Auteurs

Ilenia Sana (I)

Cell signaling Unit, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, Milano, Italy.

Maria Elena Mantione (ME)

Cell signaling Unit, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, Milano, Italy.

Miriam Meloni (M)

Cell signaling Unit, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, Milano, Italy.

Michela Riba (M)

Center for Omics Sciences, IRCCS San Raffaele Scientific Institute, Milano, Italy.

Pamela Ranghetti (P)

B-cell neoplasia Unit, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, Milano, Italy.

Lydia Scarfò (L)

B-cell neoplasia Unit, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, Milano, Italy.
Vita-Salute San Raffaele University, Milano, Italy.

Paolo Ghia (P)

B-cell neoplasia Unit, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, Milano, Italy.
Vita-Salute San Raffaele University, Milano, Italy.

Marta Muzio (M)

Cell signaling Unit, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, Milano, Italy.

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