TY - JOUR
T1 - Ent-11α-hydroxy-15-oxo-kaur-16-en-19-oic-acid induces apoptosis and cell cycle arrest in CNE-2Z nasopharyngeal carcinoma cells
AU - Wu, Kefeng
AU - Liu, Yi
AU - Lv, Yingnian
AU - Cui, Liao
AU - Li, Wende
AU - Chen, Jianfa
AU - Liang, Nian Ci
AU - Li, Li
PY - 2013/6
Y1 - 2013/6
N2 - Ent-11α-hydroxy-15-oxo-kaur-16-en-19-oic-acid (5F), a compound isolated from Pteris semipinnata L. (PsL), inhibits cell proliferation and induces cell apoptosis in several cancer lines. We found that 5F induced apoptosis and G2 phase cell cycle arrest in the CNE-2Z nasopharyngeal carcinoma (NPC) cells, accompanied by a decrease of NF-κB expression. 5F suppressed the viability of CNE-2Z cells in a time- and dose-dependent manner. 5F induced G2/M phase cell cycle arrest, but did not induce p21. Further analysis revealed that CNE-2Z cells harbored two p53 mutations. 5F treatment resulted in mitochondrial apoptosis, associated with increased Bax/Bcl-2 ratio, upregulation of cytochrome c in the cytosol, decreased NF-κB-p65 and increased IκB. Of note, 5F significantly sensitized CNE-2Z cells to cisplatin. 5F did not increase ROS, but reduced ROS production alone or in combination with cisplatin. Our data suggest that 5F is a potential anti-NPC drug for the development of single agent therapy and therapy in combination with cisplatin.
AB - Ent-11α-hydroxy-15-oxo-kaur-16-en-19-oic-acid (5F), a compound isolated from Pteris semipinnata L. (PsL), inhibits cell proliferation and induces cell apoptosis in several cancer lines. We found that 5F induced apoptosis and G2 phase cell cycle arrest in the CNE-2Z nasopharyngeal carcinoma (NPC) cells, accompanied by a decrease of NF-κB expression. 5F suppressed the viability of CNE-2Z cells in a time- and dose-dependent manner. 5F induced G2/M phase cell cycle arrest, but did not induce p21. Further analysis revealed that CNE-2Z cells harbored two p53 mutations. 5F treatment resulted in mitochondrial apoptosis, associated with increased Bax/Bcl-2 ratio, upregulation of cytochrome c in the cytosol, decreased NF-κB-p65 and increased IκB. Of note, 5F significantly sensitized CNE-2Z cells to cisplatin. 5F did not increase ROS, but reduced ROS production alone or in combination with cisplatin. Our data suggest that 5F is a potential anti-NPC drug for the development of single agent therapy and therapy in combination with cisplatin.
KW - Cisplatin
KW - Ent-11α-hydroxy-15-oxo-kaur-16-en-19-oic-acid
KW - NF-κB
KW - Naso-pharyngeal carcinoma
KW - p53
UR - http://www.scopus.com/inward/record.url?scp=84876213547&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84876213547&partnerID=8YFLogxK
U2 - 10.3892/or.2013.2375
DO - 10.3892/or.2013.2375
M3 - Article
C2 - 23563985
AN - SCOPUS:84876213547
SN - 1021-335X
VL - 29
SP - 2101
EP - 2108
JO - Oncology Reports
JF - Oncology Reports
IS - 6
ER -