Kim Kyung-Su, Rhee Kwang-Hyeon, Yoon Joo-Heon, Lee Jeung Gweon, Lee Joo-Hwan, Yoo Jong-Bum
Department of Otorhinolaryngology, Yonsei University College of Medicine, 134 Shinchon-dong, Seodaemoon-gu, Seoul, Korea.
Oral Oncol. 2005 Apr;41(4):383-9. doi: 10.1016/j.oraloncology.2004.09.013.
We have investigated whether Ginkgo biloba extract (EGb 761) induces apoptosis of oral cavity cancer cells and attempted to characterize the apoptotic pathway activated by EGb 761. The inhibition of SCC 1483 oral cavity cancer cells proliferation was noted from 250 micro/ml of EGb 761. Apoptosis was observed after 24 h of incubation with 250 microg/ml EGb 761 and occurred in a time- and dose-dependent manner. Apoptosis was confirmed by DNA fragmentation and PARP cleavage. Co-treatment with the caspase inhibitor (z-VAD-fmk) inhibited apoptosis and PARP cleavage induced by EGb 761. Caspase-3 activity was upregulated by EGb 761 but reduced to the control level by co-treating with z-VAD-fmk. In summary, EGb 761 induces apoptosis of oral cavity cancer cells and caspase-3 is activated in this apoptosis. Therefore, EGb 761 may be considered as a possible chemopreventive agent against oral cavity cancer.
我们研究了银杏叶提取物(EGb 761)是否能诱导口腔癌细胞凋亡,并试图确定EGb 761激活的凋亡途径。当EGb 761浓度达到250微克/毫升时,可观察到对SCC 1483口腔癌细胞增殖的抑制作用。用250微克/毫升EGb 761孵育24小时后可观察到细胞凋亡,且呈时间和剂量依赖性。通过DNA片段化和PARP裂解证实了细胞凋亡。与半胱天冬酶抑制剂(z-VAD-fmk)共同处理可抑制EGb 761诱导的细胞凋亡和PARP裂解。EGb 761可上调半胱天冬酶-3的活性,但与z-VAD-fmk共同处理后可将其活性降低至对照水平。总之,EGb 761可诱导口腔癌细胞凋亡,且在该凋亡过程中半胱天冬酶-3被激活。因此,EGb 761可被视为一种可能的口腔癌化学预防剂。