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Vitamin C Induces Apoptosis in Human Colon Cancer Cell Line, HCT-8 Via the Modulation of Calcium Influx in Endoplasmic Reticulum and the Dissociation of Bad from 14-3-3beta
Immune Network ; : 189-195, 2012.
Article in En | WPRIM | ID: wpr-226026
Responsible library: WPRO
ABSTRACT
It has been reported that vitamin C plays an effective role in the treatment and prevention of cancer, but its specific mechanisms are still largely unknown. The incidence of colon cancer is now increasing in Korea. Therefore, we have examined here the effect of vitamin C on the induction of the apoptosis on colon cancer and its related mechanisms. We have found that remarkable increase of the apoptosis and the calcium influx in endoplasmic reticulum (ER) in human colon cancer cell line, HCT-8. However, vitamin C-induced apoptosis was effectively inhibited by the pre-treatment of BAPTA-AM (1,2-bis(o-aminophenoxy) ethane-N,N,N',N'-tetraacetic acid), which is well-known as a calcium specific chelator. During the apoptosis, we found the increase of the translocation of Bad to mitochondria from cytosol, after releasing from 14-3-3beta. In this process, the expression of Bax, a well-known pro-apoptotic protein, was also increased. Taken together, vitamin C induces apoptosis of colon cancer cell line, HCT-8 through the increase of 1) the calcium influx in endoplasmic reticulum (ER), 2) the translocation of Bad to mitochondria, and 3) the expression of Bax.
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Full text: 1 Index: WPRIM Main subject: Ascorbic Acid / Vitamins / Cell Line / Calcium / Incidence / Egtazic Acid / Apoptosis / Colon / Colonic Neoplasms / Cytosol Type of study: Incidence_studies / Prognostic_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: Immune Network Year: 2012 Type: Article
Full text: 1 Index: WPRIM Main subject: Ascorbic Acid / Vitamins / Cell Line / Calcium / Incidence / Egtazic Acid / Apoptosis / Colon / Colonic Neoplasms / Cytosol Type of study: Incidence_studies / Prognostic_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: Immune Network Year: 2012 Type: Article