Peng Sheng-Yao, Lin Li-Ching, Chen Shu-Rong, Farooqi Ammad A, Cheng Yuan-Bin, Tang Jen-Yang, Chang Hsueh-Wei
Department of Biomedical Science and Environmental Biology, Ph.D Program in Life Sciences, College of Life Sciences, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
Department of Radiation Oncology, Chi-Mei Foundation Medical Center, Tainan 71004, Taiwan.
Antioxidants (Basel). 2021 Jul 13;10(7):1117. doi: 10.3390/antiox10071117.
The anticancer effect of pomegranate polyphenolic extract POMx in oral cancer cells has rarely been explored, especially where its impact on mitochondrial functioning is concerned. Here, we attempt to evaluate the proliferation modulating function and mechanism of POMx against human oral cancer (Ca9-22, HSC-3, and OC-2) cells. POMx induced ATP depletion, subG1 accumulation, and annexin V/Western blotting-detected apoptosis in these three oral cancer cell lines but showed no toxicity to normal oral cell lines (HGF-1). POMx triggered mitochondrial membrane potential (MitoMP) disruption and mitochondrial superoxide (MitoSOX) generation associated with the differential downregulation of several antioxidant gene mRNA/protein expressions in oral cancer cells. POMx downregulated mitochondrial mass, mitochondrial DNA copy number, and mitochondrial biogenesis gene mRNA/protein expression in oral cancer cells. Moreover, POMx induced both PCR-based mitochondrial DNA damage and γH2AX-detected nuclear DNA damage in oral cancer cells. In conclusion, POMx provides antiproliferation and apoptosis of oral cancer cells through mechanisms of mitochondrial impairment.
石榴多酚提取物POMx对口腔癌细胞的抗癌作用鲜有研究,尤其是其对线粒体功能的影响。在此,我们试图评估POMx对人口腔癌(Ca9-22、HSC-3和OC-2)细胞的增殖调节功能及其机制。POMx在这三种口腔癌细胞系中诱导ATP耗竭、亚G1期积累以及膜联蛋白V/蛋白质印迹法检测到的细胞凋亡,但对正常口腔细胞系(HGF-1)无毒性。POMx引发线粒体膜电位(MitoMP)破坏和线粒体超氧化物(MitoSOX)生成,这与口腔癌细胞中几种抗氧化基因mRNA/蛋白质表达的差异下调有关。POMx下调口腔癌细胞中的线粒体质量、线粒体DNA拷贝数以及线粒体生物发生基因mRNA/蛋白质表达。此外,POMx在口腔癌细胞中诱导基于PCR的线粒体DNA损伤以及γH2AX检测到的核DNA损伤。总之,POMx通过线粒体损伤机制实现口腔癌细胞的抗增殖和凋亡作用。