Research Article

ROS-Mediated Mitochondrial Pathway is Required for Manilkara Zapota (L.) P. Royen Leaf Methanol Extract Inducing Apoptosis in the Modulation of Caspase Activation and EGFR/NF-κB Activities of HeLa Human Cervical Cancer Cells

Table 2

Treatment of Manilkara zapota leaf methanol extract (1.56-200 μg/mL) on selected cancer cell lines for 24, 48, and 72 h evaluated by MTT and LDH assays.

Cancer cell linesMTT (μg/mL)LDH (μg/mL)
24 h48 h72 h24 h48 h72 h

HT-2993.27 ± 17.1989.29 ± 6.0169.12 ± 8.1090.33 ± 15.7985.99 ± 4.8776.22 ± 5.39
HCT-11690.14 ± 14.2387.33 ± 9.2983.17 ± 9.9293.22 ± 9.0390.12 ± 9.7788.11 ± 11.69
HeLa89.29 ± 18.2059.23 ± 10.3323.87 ± 5.0287.33 ± 14.9880.44 ± 11.6525.76 ± 8.93
HGT-180.11 ± 10.1972.04 ± 5.2349.44 ± 10.6265.20 ± 14.2762.11 ± 6.2959.89 ± 10.27
HepG297.29 ± 3.2683.95 ± 9.2073.02 ± 9.3389.45 ± 16.8283.03 ± 5.3577.04 ± 9.93

HCT-116: human colon carcinoma, HeLa: human cervical cancer, HepG2: human hepatocellular carcinoma, HGT-1: human gastric adenocarcinoma, HT-29: human colorectal adenocarcinoma, LDH: lactate dehydrogenase, and MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide.
Values are reported as mean ± SD (n = 3). Value with different superscript letter in the same row for their respective assay indicates significant difference by Tukey’s test (P < 0.05). In MTT assay, treatment with Manilkara zapota leaf methanol extract for 72 h (69.12 ± 8.10 μg/mL) significantly inhibited the proliferation of HT-29 cells compared to 24 h (93.27 ± 17.19 μg/mL) (P < 0.05), whereas, in LDH assay, there was a significant effect of the cytotoxic activities of Manilkara zapota leaf methanol extract in HT-29 cells incubated for 72 h (76.22 ± 5.39 μg/mL) compared to those incubated for 24 h (90.33 ± 15.79 μg/mL) or 48 h (85.99 ± 4.87 μg/mL) (P < 0.05).