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Untargeted metabolomics using UHPLC-Q-Orbitrap HRMS for identifying cytotoxic compounds on MCF-7 breast cancer cells from Annona muricata Linn leaf extracts as potential anticancer agents.
Septaningsih, Dewi Anggraini; Suparto, Irma Herawati; Achmadi, Suminar Setiati; Heryanto, Rudi; Rafi, Mohamad.
  • Septaningsih DA; Department of Chemistry, Faculty of Mathematics and Natural Sciences, IPB University, Bogor, Indonesia.
  • Suparto IH; Advance Research Laboratory, IPB University, Bogor, Indonesia.
  • Achmadi SS; Department of Chemistry, Faculty of Military Mathematics and Natural Sciences, Indonesian Defense University, Bogor, Indonesia.
  • Heryanto R; Department of Chemistry, Faculty of Mathematics and Natural Sciences, IPB University, Bogor, Indonesia.
  • Rafi M; Tropical Biopharmaca Research Center, IPB University, Bogor, Indonesia.
Phytochem Anal ; 35(6): 1418-1427, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38708435
ABSTRACT

INTRODUCTION:

The leaves of Annona muricata L., known as "soursop" or "sirsak" in Indonesia, are used traditionally for cancer treatment. However, the bioactive components remain largely unidentified.

OBJECTIVE:

This study used untargeted liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based metabolomics to identify potential cytotoxic compounds in A. muricata leaf extracts on MCF-7 breast cancer cells in vitro.

METHODS:

A. muricata leaves were macerated with water, 99% ethanol, and aqueous mixtures containing 30%, 50%, and 80% ethanol. Cytotoxic activity of the extracts against MCF-7 breast cancer cells was determined using the MTT assay. Ultra-high-performance liquid chromatography-Q-Orbitrap high-resolution mass spectroscopy (UHPLC-Q-Orbitrap-HRMS) was used to characterize the metabolite composition of each extract. The correlations between metabolite profile and cytotoxic activities were evaluated using orthogonal partial least square discriminant analysis (OPLS-DA). The binding of these bioactive compounds to the tumorigenic alpha-estrogen receptor (3ERT) was then evaluated by in silico docking simulations.

RESULTS:

Ninety-nine percent ethanol extracts demonstrated the greatest potency for reducing MCF-7 cell viability (IC50 = 22 µg/ml). We detected 35 metabolites in ethanol extracts, including alkaloids, flavonoids, and acetogenins. OPLS-DA predicted that annoreticuin, squadiolin C, and xylopine, and six unknown acetogenin metabolites, might reduce MCF-7 cell viability. In silico analysis predicted that annoreticuin, squadiolin C, and xylopine bind to 3ERT with an affinity comparable to doxorubicin.

CONCLUSION:

Untargeted metabolomics and in silico modeling identified cytotoxic compounds on MCF-7 cells and binding affinity to 3ERT in A. muricata leaf extracts. The findings need to be further verified to prove the screening results.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Extractos Vegetales / Hojas de la Planta / Annona / Espectrometría de Masas en Tándem / Metabolómica / Antineoplásicos Fitogénicos Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Extractos Vegetales / Hojas de la Planta / Annona / Espectrometría de Masas en Tándem / Metabolómica / Antineoplásicos Fitogénicos Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article