Journal Article
Research Support, Non-U.S. Gov't
Add like
Add dislike
Add to saved papers

Alpinia pricei rhizome extracts induce apoptosis of human carcinoma KB cells via a mitochondria-dependent apoptotic pathway.

Alpinia pricei Hayata (A. pricei) is well known in Taiwan as a traditional Chinese medicine. In this study, the ability of ethanol (70%) extracts of A. pricei rhizome (AP extracts) to induce apoptosis in cultured human carcinoma KB cells was investigated. Treatment of KB cells with various concentrations of AP extracts (25-200 microg/mL) resulted in sequences of events marked by apoptosis, such as loss of cell viability, morphology change, and internucleosomal DNA fragmentation. AP extract-induced apoptotic cell-death was associated with loss of mitochondrial membrane potential, cytochrome c translocation, caspase-3 and -9 activation, and poly ADP-ribose polymerase (PARP) degradation in KB cells. This increase in AP extract-induced apoptosis was also associated with a reduction in the levels of Bcl-2, a potent cell-death inhibitor, and an increase in levels of the Bax protein, which heterodimerizes with and thereby inhibits Bcl-2. Furthermore, AP extracts induced a dose-dependent elevation of reactive oxygen species (ROS) in KB cells. Our findings suggest that A. pricei exerts antiproliferative action and growth inhibition on human carcinoma KB cells through a mitochondria-dependent apoptotic pathway. A. pricei may, therefore, have anticancer properties valuable for application in food and drug products.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app