The Autoxidized Mixture of (-)-Epicatechin Contains Procyanidins and Shows Antiproliferative and Apoptotic Activity in Breast Cancer Cells.
Yazmin Osorio-CruzIvonne María Olivares-CorichiCorrea-Basurto JoséJosé Arnold González-GarridoFernando Pereyra-VergaraGildardo RiveraJosé Rubén García-SánchezPublished in: Pharmaceuticals (Basel, Switzerland) (2024)
For this study, procyanidins generated through the autoxidation of (-)-epicatechin (Flavan-3-ol) under mildly acidic conditions (pH = 6.0) were characterized with ultra high-performance liquid chromatography (UHPLC) coupled with tandem mass spectrometry (MS/MS). Two procyanidins (types A and B) and a mix of oligomers were generated through the autoxidation of (-)-epicatechin. The antiproliferative activity of this mixture of procyanidins on MDA-MB-231, MDA-MB-436, and MCF-7 breast cancer cells was evaluated. The results indicate that the procyanidin mixture inhibited the proliferation of breast cancer cells, where the activity of the procyanidin mixture was stronger than that of (-)-epicatechin. Moreover, the mechanism underlying the antiproliferative activity of procyanidins was investigated. The resulting data demonstrate that the procyanidins induced apoptotic cell death in a manner selective to cancerous cells. In particular, they caused the activation of intrinsic and extrinsic apoptotic pathways in the breast cancer cells. The findings obtained in this study demonstrate that the generation of procyanidins in vitro by the autoxidation of (-)-epicatechin has potential for the development of anti-breast cancer agents.
Keyphrases
- breast cancer cells
- tandem mass spectrometry
- ultra high performance liquid chromatography
- cell death
- ms ms
- cell cycle arrest
- simultaneous determination
- high performance liquid chromatography
- liquid chromatography
- high resolution mass spectrometry
- gas chromatography
- solid phase extraction
- high resolution
- signaling pathway
- anti inflammatory
- mass spectrometry
- induced apoptosis
- machine learning
- big data
- cell proliferation
- artificial intelligence
- drug induced
- endoplasmic reticulum stress
- atomic force microscopy
- childhood cancer