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Steviol, a natural product inhibits proliferation of the gastrointestinal cancer cells intensively.


ABSTRACT: New anticancer agents with lower toxicity have been always urged because of drug resistance associated with overused chemotherapy agents. In this study, steviol, a colonic metabolite of natural sweetener and also a component in leaves of stevia rebaudiana bertoni, was found to possess intensive anticancer activity on the human gastrointestinal cancer cells. Steviol inhibited six human gastrointestinal cancer cells intensively as 5-fluorouracil did at 100 ?g/mL. The inhibition mechanism follows mitochondrial apoptotic pathway that was evidenced by increase of Bax/Bcl-2 ratio, activation of p21 and p53; and caspase 3-independent mechanism was also involved. These results are consistent with the miRNA expression analysis. The most regulated miRNAs in the steviol treated gastrointestinal cancer cells were miR-203a-3p (log2 =1.32) and miR-6088 (log2 =-2.54) in HCT-116, miR-1268b (log2 =19.85) and miR-23c (log2 =-2.05) in MKN-45. In view of the metabolic characteristics of steviol and its cytotoxicity on the cancer cells, steviol could be a chemotherapy agent potentially for cancer treatment.

SUBMITTER: Chen J 

PROVIDER: S-EPMC5995179 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature

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Steviol, a natural product inhibits proliferation of the gastrointestinal cancer cells intensively.

Chen Junming J   Xia Yongmei Y   Sui Xiaochen X   Peng Qingrui Q   Zhang Tongtong T   Li Jian J   Zhang Jue J  

Oncotarget 20180529 41


New anticancer agents with lower toxicity have been always urged because of drug resistance associated with overused chemotherapy agents. In this study, steviol, a colonic metabolite of natural sweetener and also a component in leaves of <i>stevia rebaudiana bertoni</i>, was found to possess intensive anticancer activity on the human gastrointestinal cancer cells. Steviol inhibited six human gastrointestinal cancer cells intensively as 5-fluorouracil did at 100 μg/mL. The inhibition mechanism fo  ...[more]

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