Planta Medica · 2021 · 10 citations · 22 references
MedicineMedicinal ChemistryPharmacologyApoptosisChemotherapyMolecular OncologyApoptosis PharmacologyCell Cycle PharmacologyCytotoxic ChemotherapyOncology PharmacologyAnticancer ActivityApoptosis InductionCancer Cell Proliferation InhibitionCell Cycle InhibitionMtor InhibitionMtor SignalingPi3k-akt Signaling PathwayPi3k-akt-mtor Signaling
Graib. Their structures were elucidated by spectral methods and compared with literature data. To evaluate their anti-proliferative effects in tumor cells, firstly, cisplatin was used as a positive control and the effects of compound 1: - 3: were determined by performing MTT assay in MDA-MB-231, CNE-2 and A549 cancer cells. The results showed compound 1: - 3: exhibited stronger inhibitory effect than cisplatin in MDA-MB-231. Further effects of compound 1: - 3: in TNBC MDA-MB-231 and MDA-MB-468 cells were examined by performing cell cycle and apoptosis assays. The results indicated that compound 1: - 3: had ability to arrest cell cycle at G2/M phase and induce apoptosis. Furthermore, compound 2: significantly down-regulated PI3K, Akt and mTOR levels in both total proteins and phosphorylated form, which is its potential anti-cancer mechanism. These findings indicated that those prenylated xanthones might serve as promising leading compounds for the development of anticancer drug for TNBC.
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John C. Reed · American Journal Of Pathology · 2000 · 1.3K citations · Full text
An overview on genus garcinia: phytochemical and therapeutical aspects
Mahadevappa Hemshekhar, K. Sunitha, M. Sebastin Santhosh et al. · Phytochemistry Reviews · 2011 · 181 citations