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Enregistrement W2547033671 · doi:10.1182/blood.v120.21.3879.3879

Inhibition of Fatty Acid Oxidation Leads to Apoptosis of Resting and Proliferating Chronic Lymphocytic Leukemia Cells in Vitro

2012· article· en· W2547033671 sur OpenAlexaff
Davorka Messmer, Kymmy Lorrain, Yalda Bravo, Nicholas Stock, Richard A. Bundey, Lucia Correa, Michael M. Poon, Karin J. Stebbins, Géraldine Cabrera, Austin Chen, Jason Jacintho, David Spaner, Peppi Prasit, Daniel S. Lorrain

Notice bibliographique

RevueBlood · 2012
Typearticle
Langueen
DomaineBiochemistry, Genetics and Molecular Biology
ThématiqueCancer, Lipids, and Metabolism
Établissements canadiensSunnybrook Health Science Centre
Organismes subventionnairesnon disponible
Mots-clésChronic lymphocytic leukemiaApoptosisFludarabineCancer researchBeta oxidationLeukemiaCancer cellBiologyContext (archaeology)In vitroFatty acidChemistryPharmacologyCancerImmunologyBiochemistryChemotherapy

Résumé

récupéré en direct d'OpenAlex

Abstract Abstract 3879 Tumor-specific metabolic changes could serve as new therapeutic targets. While much attention has been given to the metabolism of glucose in cancer cells and intervening therapies, relatively little attention has been given to fatty acids and fatty acid β-oxidation (FAO) in promoting cancer cell survival. Here, we reveal new findings implicating fatty acid metabolism in Chronic lymphocytic leukemia (CLL) and have developed a small molecule inhibitor of this pathway as a novel therapeutic approach to treat CLL. We have found that B cells isolated from CLL patients show increased levels of b-oxidation as compared to B cells isolated from PBMCs of healthy donor controls. NXT629, a small molecule inhibitor of the FAO pathway, dose-dependently reduced b-oxidation in CLL cells but did not reduce b-oxidation in B cells isolated from healthy volunteers. A negative control compound (NXT962) that has a similar chemical structure to NXT629, but does not significantly bind to the relevant target, did not inhibit FAO. NXT629 exerted dose-dependent cytotoxicity in CLL cells (CC50=10 mM, n=5 different patient samples) whereas NXT962 was inactive. Since the cellular microenvironment can protect CLL cells from spontaneous and drug-induced apoptosis, it is pivotal to evaluate novel drugs in this context. As expected, we found that macrophages protected CLL cells from spontaneous and fludarabine-induced apoptosis in vitro. However, NXT629 significantly reduced CLL cells viablity in the co-cultures. NXT629 (at 10 mM, n=2 different patient samples) induced apoptosis in 80% of cells after 7 days of co-culture in a setting where fludarabine was inactive. Though most CLL cells in the periphery are in a resting state, CLL cells proliferate in lymphoid organs. To mimic these conditions, we examined the activity of FAO inhibition on CLL cells that were induced to proliferate in vitro. To induce proliferation, CLL cells were cultured in media containing human interleukin (IL)-4, IL-10, and allogeneic T blasts. Labeling CLL cells with carboxyfluorescein succinimidyl ester, allowed us to monitor several rounds of induced CLL-cell division via flow cytometry, and within 5 days the CLL cells had expanded 3-fold. We found that addition of NXT629 to such cultures resulted in a dose-dependent reduction in the number of leukemia cells induced to undergo cell-division (IC50=3.7 mM, n=6), whereas the negative control compound showed no activity. Furthermore, when used in combination with dexamethasone (0.3 mM), NXT629 (3 mM) showed a significant decrease in the number of viable cells (38% +/−3%) over either dexamethasone (65% +/−12%) or NXT629 (74%+/−15%) alone. The additivity of FAO inhibition and dexamethasone in vitro suggests that a combination warrants further testing and might yield improved clinical responses. Overall, these results suggest that fatty acids promote primary CLL cell survival and proliferation, and that targeting the FAO pathway could be a new therapeutic approach to treating CLL. Disclosures: Messmer: Inception Sciences: Employment, Equity Ownership. Lorrain:Inception Sciences: Employment, Equity Ownership. Bravo:Inception Sciences: Employment, Equity Ownership. Stock:Inception Sciences: Employment, Equity Ownership. Bundey:Inception Sciences: Employment, Equity Ownership. Correa:Inception Sciences: Employment, Equity Ownership. Poon:Inception Sciences: Employment, Equity Ownership. Stebbins:Inception Sciencees: Employment, Equity Ownership. Cabrera:Inception Sciences: Employment, Equity Ownership. Chen:Inception Sciences: Employment, Equity Ownership. Jacintho:Inception Sciences: Employment, Equity Ownership. Spaner:Inception Sciences: Consultancy, Equity Ownership, Membership on an entity's Board of Directors or advisory committees, Research Funding. Prasit:Inception Sciences: Employment, Equity Ownership, Membership on an entity's Board of Directors or advisory committees. Lorrain:Inception Sciences: Employment, Equity Ownership.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction machine sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.

score de la tête « metaresearch » (Codex)0,000
score de la tête « metaresearch » (Gemma)0,000
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Expérimental (laboratoire) · Signal consensuel: Expérimental (laboratoire)
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,003
Score d'incertitude au seuil0,009

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0000,000
Méta-épidémiologie (sens strict)0,0010,000
Méta-épidémiologie (sens large)0,0000,000
Bibliométrie0,0000,000
Études des sciences et des technologies0,0000,000
Communication savante0,0000,000
Science ouverte0,0000,000
Intégrité de la recherche0,0000,001
Charge utile insuffisante (le modèle a refusé de juger)0,0030,001

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,009
Tête enseignante GPT0,230
Écart entre enseignants0,222 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeExpérimental (laboratoire)
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations1
Publié2012
Routes d'admission1
Résumé présentoui

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