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Chrysanthemum Extract Appears Promising for Cancer Treatment

By LabMedica International staff writers
Posted on 13 Nov 2009
A series of studies have demonstrated that Chrysanthemum indicum extract possesses antimicrobial, anti-inflammatory, immunomodulatory, and neuroprotective effects. More...
Recently, much attention has been devoted to the anticancer activity of the extract, particularly in hepatocellular carcinoma (HCC).

However, its anticancer mechanism of action is still not clear and needs further investigation. A research article published on September 28, 2009, in the World Journal of Gastroenterology addressed this question. The research team, led by Prof. Zong-fang Li from the Second Affiliated Hospital, School of Medicine, Xi'an Jiaotong University (Xi'an, Shaanxi Province, China), investigated the effects of C. indicum extract (CIE) on the inhibition of proliferation and on apoptosis, and the underlying mechanisms, in a human HCC MHCC97H cell line.

The investigators examined viable rat hepatocytes and human endothelial ECV304 cells by trypan blue exclusion and MTT assay, respectively, as normal controls. The proliferation of MHCC97H cells was determined by MTT assay. The cellular morphology of MHCC97H cells was observed by phase contrast microscopy. Flow cytometry was performed to analyze cell apoptosis with annexin V/propidium iodide (PI), mitochondrial membrane potential with rhodamine 123, and cell cycle with PI in MHCC97H cells. Apoptotic proteins such as cytochrome C, caspase-9, caspase-3 and cell cycle proteins, including P21 and CDK4, were measured by Western blotting.

The study's findings showed CIE inhibited proliferation of MHCC97H cells in a time- and dose-dependent manner without cytotoxicity in rat hepatocytes and human endothelial cells. CIE induced apoptosis of MHCC97H cells in a concentration-dependent manner, as determined by flow cytometry. The apoptosis was accompanied by a decrease in mitochondrial membrane potential, release of cytochrome C and activation of caspase-9 and caspase-3. CIE arrested the cell cycle in the S phase by increasing P21 and decreasing CDK4 protein expression.

The researchers concluded that CIE exerted a significant apoptotic effect through a mitochondrial pathway and arrested the cell cycle by regulation of cell cycle-related proteins in MHCC97H cells without an effect on normal cells. The cancer-specific selectivity shown in their study suggests that the plant extract could be a promising novel treatment for human cancer.

Related Links:
Second Affiliated Hospital, School of Medicine, Xi'an Jiaotong University




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