Prenylated xanthones from mangosteen (Garcinia mangostana) target oxidative mitochondrial respiration in cancer cells.

Garcinia mangostana Mitochondrial membrane potential OXPHOS Prenylated xanthones Proton leak Superoxides

Journal

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
ISSN: 1950-6007
Titre abrégé: Biomed Pharmacother
Pays: France
ID NLM: 8213295

Informations de publication

Date de publication:
31 Aug 2024
Historique:
received: 10 06 2024
revised: 22 08 2024
accepted: 26 08 2024
medline: 2 9 2024
pubmed: 2 9 2024
entrez: 1 9 2024
Statut: aheadofprint

Résumé

Mangosteen (Garcinia mangostana) is well-known for its nutritional value and health benefits. Breast cancer is the most common cancer and the leading cause of cancer-related mortality among females worldwide. Here we show that the prenylated xanthones, α-mangostin, γ-mangostin, 9-hydroxycalabaxanthone (9-HCX), and garcinone E from the mangosteen pericarp exhibit cytotoxicity against a panel of human cancer cell lines including lung adenocarcinoma (A549), cervical carcinoma (HeLa), prostatic carcinoma (DU 145), pancreatic carcinoma (MIA PaCa-2), hepatocellular carcinoma (Hep G2), bladder urothelial cancer (5637), as well as the triple-negative breast cancer cells MDA-MB-231. In line with its higher predicted bioactivity score compared to other prenylated xanthones, 9-HCX induced the strongest antiproliferative and proapoptotic effects in MDA-MB-231 breast cancer xenografts in vivo. In different in vitro models, we demonstrate that prenylated xanthones from G. mangostana target mitochondria in cancer cells by inhibition of the mitochondrial respiratory chain complex II (α-mangostin, γ-mangostin, and garcinone E) and complex III (9-HCX) as shown in isolated mitochondria. Accordingly, oxidative mitochondrial respiration (OXPHOS) was inhibited, mitochondrial proton leak increased, and adenosine triphosphate (ATP) synthesis decreased as analyzed by Seahorse assay in MDA-MB-231 cells. Hence, the prenylated xanthones increased mitochondrial superoxide levels, induced mitochondrial membrane permeabilization, and initiated caspase 3/7-mediated apoptosis in MDA-MB-231 triple-negative breast cancer cells. Thus, prenylated xanthones from Garcinia mangostana exhibit anticancer activity based on interference with the mitochondrial respiration.

Identifiants

pubmed: 39217837
pii: S0753-3322(24)01250-2
doi: 10.1016/j.biopha.2024.117365
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

117365

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Masson SAS.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors have stated that there is no conflict of interest associated with the publication and no financial support, which could have influenced the outcome.

Auteurs

Menna El Gaafary (M)

Institute of Experimental and Clinical Pharmacology, Toxicology, and Pharmacology of Natural Products, Ulm University, D-89081 Ulm, Germany; Department of Analytical Chemistry, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt. Electronic address: mennat_elgaafary@yahoo.com.

Passent M Abdel-Baki (PM)

Department of Analytical Chemistry, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt. Electronic address: passent.mohamed@pharma.cu.edu.eg.

Ali M El-Halawany (AM)

Department of Analytical Chemistry, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt. Electronic address: ali.elhalawany@pharma.cu.edu.eg.

Heba M Mohamed (HM)

Department of Analytical Chemistry, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt; Faculty of Health Sciences, Higher Colleges of Technology, Dubai, United Arab Emirates. Electronic address: heba.moustafa@pharma.cu.edu.eg.

Amira Duweb (A)

Institute of Experimental and Clinical Pharmacology, Toxicology, and Pharmacology of Natural Products, Ulm University, D-89081 Ulm, Germany; Department of Pharmacology, Faculty of Medicine, University of Tripoli, Tripoli, Libya. Electronic address: amira.duweb@uni-ulm.de.

Hossam M Abdallah (HM)

Institute of Experimental and Clinical Pharmacology, Toxicology, and Pharmacology of Natural Products, Ulm University, D-89081 Ulm, Germany; Department of Natural Products and Alternative Medicine, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia. Electronic address: hmafifi@kau.edu.sa.

Gamal A Mohamed (GA)

Department of Natural Products and Alternative Medicine, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia. Electronic address: gahussein@kau.edu.sa.

Sabrin R M Ibrahim (SRM)

Preparatory Year Program, Department of Chemistry, Batterjee Medical College, Jeddah 21442, Saudi Arabia; Department of Pharmacognosy, Faculty of Pharmacy, Assiut University, Assiut 71526, Egypt. Electronic address: sabrin.ibrahim@bmc.edu.sa.

Thomas Simmet (T)

Institute of Experimental and Clinical Pharmacology, Toxicology, and Pharmacology of Natural Products, Ulm University, D-89081 Ulm, Germany. Electronic address: thomas.simmet@uni-ulm.de.

Tatiana Syrovets (T)

Institute of Experimental and Clinical Pharmacology, Toxicology, and Pharmacology of Natural Products, Ulm University, D-89081 Ulm, Germany. Electronic address: tatiana.syrovets@uni-ulm.de.

Classifications MeSH