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Anti-Cancer Effect of Resveratrol is Associated with Induction of Apoptosis via a Mitochondrial Pathway Alignment.

Authors :
Back, Nathan
Cohen, Irun R.
Lajtha, Abel
Lambris, John D.
Paoletti, Rodolfo
Kang, Kyung A.
Harrison, David K.
Bruley, Duane F.
Sun, Weimin
Wang, Wei
Kim, Jung
Keng, Peter
Yang, Shanmin
Zhang, Hengshan
Liu, Chaomei
Okunieff, Paul
Zhang, Lurong
Source :
Oxygen Transport to Tissue XXIX; 2008, p179-186, 8p
Publication Year :
2008

Abstract

Resveratrol, a phytoalexin found in the skin of grapes, is believed to have multiple bioactivities including anti-cancer, anti-carcinogenesis and antiinflammatory. The mechanisms by which resveratrol might produce these effects are not well understood. In this study, malignant human pancreatic cancer cells were treated without or with resveratrol in combination with ionizing radiation (IR), and then the mitochondrial function of treated cells was evaluated using several standardized assays. They include the CalceinAMmethod for mitochondria transition pore; the JC-1 staining method for mitochondria membrane potential; the CM-H2DCFDA method for reactive oxygen species; and the Annexin V/propidium iodide (PI) method for apoptosis/cell death. Our results indicated that (1) pore function was partially intact after resveratrol, but resveratrol probably interfered with the accumulation of intracellular Calcein AM; (2) depolarization of the mitochondria membrane was increased in the resveratrol treated cells, consistent with mitochondrial dysfunction; (3) ROS was slightly increased with resveratrol, a phenomenon that was greatly increased when this agent was combined with IR; and (4) in parallel with the above changes in mitochondrial and drug transport, cells treated with resveratrol showed increased apoptosis as measured by Annexin V/PI staining. In summary, the anti-cancer effect of resveratrol is associated with the damage of mitochondrial function that leads to increased ROS, apoptosis, and possibly intracellular drug accumulation via inhibition of proteins involved in multi-drug resistance (MDR). [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISBNs :
9780387749105
Database :
Supplemental Index
Journal :
Oxygen Transport to Tissue XXIX
Publication Type :
Book
Accession number :
33755071
Full Text :
https://doi.org/10.1007/978-0-387-74911-2_21