Date of Award
10-2013
Degree Type
Thesis
Degree Name
Master of Science (MS)
First Advisor
Dianzheng Zhang, PhD
Second Advisor
Denah M Appelt, PhD
Third Advisor
Ruth Borghaei, PhD
Abstract
Radiotherapy and surgery are the two principal modalities in the treatment of head and neck cancers, and both therapies can result in severe adverse effects and ultimately lower the quality of life. It is of paramount importance to develop reagents that target the cancer cell specifically without affecting the normal non-cancer cells. Using the tongue cancer cell line Cal 27 as a model system, we dissected the molecular mechanism of the resveratrol-induced cancer cell apoptosis. After demonstrating that resveratrol induces the cancer cell apoptosis in a dose- and time-dependent manner, a systemic apoptosis protein array was conducted to identify the resveratrol-induced proteins pertinent to the apoptotic pathways. Ten of the 43 proteins included in the array were up- or down-regulated by resveratrol by about 50 percent. Finally, the activation of caspase-3 and the cleavage of PARP in resveratrol-induced apoptotic cells were confirmed by western blot. We postulate resveratrol induces apoptosis in Cal-27 cells which will render the cells from being able to repair double-stranded-break in the DNA as both P53 and P21 will be up regulated and thus leading to senesce of the cell replication, suggesting that resveratrol could potentially serve as a chemo-preventive reagent.
Recommended Citation
Siddiqi, Saquib A., "Resveratrol Induced Apoptosis in a Human Adenosquamous Carcinoma Cell Line (CAL-27 Cells)" (2013). PCOM Biomedical Studies Student Scholarship. 79.
https://digitalcommons.pcom.edu/biomed/79