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Cytotoxicity Effect and Morphological Changes of Chrysanthemum Morifolium Methanolic Extract against Chronic Myeloid Leukaemia K-562 Cell Line
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Chrysanthemum morifolium, also known as “Bunga kekwa” in Malaysia, has various benefits and widely used in Chinese herbal medicines. The plant extract was reported to have significant biological activities, such as anti-inflammation, anti-tumour, anti-oxidant, and anti-cancer. Nonetheless, its anti-cancer potential on chronic myeloid leukaemia has remained elusive. The main goal of this study is to evaluate the cytotoxic effect of C.morifolium buds and flowers in methanolic extracts on chronic myeloid leukaemia malignancy K-562 cell lines. The bud and flower of C.morifolium were macerated for 72 hours in 100% methanol then were concentrated under reduced pressure using a rotary evaporator and oven-dried to obtain crude extracts. K-562 cells were treated with six different concentrations 400, 200, 100, 50, 25, and 12.5 µg/ml and incubated for 24, 48 and 72 hours. The in vitro cytotoxic activity was measured using the 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazolium bromide (MTT) test and was quantified using a microplate reader at 570 nm. Acridine orange and propidium iodide (AO/PI) staining were used to assess morphological alterations. MTT assays results showed moderate toxicity of both extracts. The lowest maximal half inhibitory concentration (IC50) value were observed at 72 hours of incubation; 182 ± 4.04 ug/ml for BM and 161 ± 7.88 ug/ml for flower extract (FM). However, there was a significantly different IC50 value (p<0.05) between the incubation periods of both treatments where the IC50 value at 24 hours was 301.33 ± 8.51 ug/ml 301 µg/ml in BM, 216 ± 10.79 ug/ml 216 µg/ml in FM and at 48 hours was 227 ± 12.25 ug/ml 227 µg/ml in bud extract (BM), 174 ± 11.92 ug/ml 174 µg/ml in FM. The morphological changes evidence was shown in AO/PI staining by the appearance of a mixed population of cells; early apoptosis, late apoptosis and necrotic cells. These findings suggested that methanolic C.morifolium extracts showed moderate cytotoxic effect on chronic myeloid leukaemia K-562 cells. Further study needed to identify the mode and mechanism of cell death in K-562 cells treated with the C.morifolium extracts.
Title: Cytotoxicity Effect and Morphological Changes of Chrysanthemum Morifolium Methanolic Extract against Chronic Myeloid Leukaemia K-562 Cell Line
Description:
Chrysanthemum morifolium, also known as “Bunga kekwa” in Malaysia, has various benefits and widely used in Chinese herbal medicines.
The plant extract was reported to have significant biological activities, such as anti-inflammation, anti-tumour, anti-oxidant, and anti-cancer.
Nonetheless, its anti-cancer potential on chronic myeloid leukaemia has remained elusive.
The main goal of this study is to evaluate the cytotoxic effect of C.
morifolium buds and flowers in methanolic extracts on chronic myeloid leukaemia malignancy K-562 cell lines.
The bud and flower of C.
morifolium were macerated for 72 hours in 100% methanol then were concentrated under reduced pressure using a rotary evaporator and oven-dried to obtain crude extracts.
K-562 cells were treated with six different concentrations 400, 200, 100, 50, 25, and 12.
5 µg/ml and incubated for 24, 48 and 72 hours.
The in vitro cytotoxic activity was measured using the 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazolium bromide (MTT) test and was quantified using a microplate reader at 570 nm.
Acridine orange and propidium iodide (AO/PI) staining were used to assess morphological alterations.
MTT assays results showed moderate toxicity of both extracts.
The lowest maximal half inhibitory concentration (IC50) value were observed at 72 hours of incubation; 182 ± 4.
04 ug/ml for BM and 161 ± 7.
88 ug/ml for flower extract (FM).
However, there was a significantly different IC50 value (p<0.
05) between the incubation periods of both treatments where the IC50 value at 24 hours was 301.
33 ± 8.
51 ug/ml 301 µg/ml in BM, 216 ± 10.
79 ug/ml 216 µg/ml in FM and at 48 hours was 227 ± 12.
25 ug/ml 227 µg/ml in bud extract (BM), 174 ± 11.
92 ug/ml 174 µg/ml in FM.
The morphological changes evidence was shown in AO/PI staining by the appearance of a mixed population of cells; early apoptosis, late apoptosis and necrotic cells.
These findings suggested that methanolic C.
morifolium extracts showed moderate cytotoxic effect on chronic myeloid leukaemia K-562 cells.
Further study needed to identify the mode and mechanism of cell death in K-562 cells treated with the C.
morifolium extracts.
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