When compared to the control, MCF-7 cells cultured with SCBM extract for 24 h lost their original shape at increasing concentrations. Membrane damage, cell rounding, and cell separation from the culture plates were all telltale markers of cell death. At the smallest dose, however, these effects were not observed.
Caused a 25%–50% death rate in HepG2 hepatocellular cancer cells. Colon cancer cells (HT-29; IC50 = 0.75–1.39 mg/mL), stomach cancer cells (AGS; IC50 = 0.59–1.88 mg/mL), bladder cancer cells (BL13; IC50 = 0.56–1.12 mg/mL), and liver cancer cells (HepG2; IC50 = 0.38–1.36 mg/mL) all had their proliferation inhibited by the extracts. Non-transformed colon cells (CCD-18Co; IC50 > 2.0 mg/mL) and stomach/intestine cells (Hs 738. St/Int; IC50 > 2.0 mg/mL) showed no discernible loss of viability.
The IC50 values for the essential oil were 59.9 μg/mL and 47.5 μg/mL for the HCT-116 and human ovarian teratocarcinoma cells (Pa-1) cell lines, respectively.
Compared to the chemotherapy drug gemcitabine, the extract (200 μg/mL) dramatically decreased the vitality of MiaPaCa-2 and ASPC-1 pancreatic cancer cells.
Reduced ATP levels (47.96%) and elevated lactate dehydrogenase (LDH) levels (40.96%) in MCF-7 cells were indicative of solitary metachronous bone metastasis (SMBM)-induced toxicity.
And at 40 μg/mL, Syzygium coriaceum caused an 88.1% (P < 0.0001) decrease in mitochondrial membrane potential, a 5.7% (P < 0.0001) increase in the number of the cell population in G0/G1, and an increased (P < 0.0001) proportion of cells experiencing apoptotic/necrotic cell death.
Dose-dependent elevation of ROS was observed after extract treatment in HepG2 cells, with a 4.4-fold rise at 100 mg/mL (P < 0.0001). The dose-dependent reduction in antioxidant enzyme activity mirrored the increase in ROS concentration. At 40 μg/mL (P < 0.0001), glutathione peroxidase activity dropped by 80.5%.
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