Lee Jun, Lee Hwa-Jeong, Park Jong-Dae, Lee Sun-Kyung, Lee Sang-Im, Lim Hyun-Dae, Lee You-Mee, Yun Young-Gab, Jeon Byung-Hun, Ree In-Soo, Jun Chang-Duk, Lee Suk-Keun, Kim Eun-Cheol
Department of Oral and Maxillofacial Surgery, College of Dentistry, Wonkwang University, Iksan, South Korea.
Toxicol In Vitro. 2008 Feb;22(1):87-95. doi: 10.1016/j.tiv.2007.08.016. Epub 2007 Sep 1.
Sulfur is commonly used in Asia as an herbal medicine to treat inflammation and cancer, and potent chemopreventive effects have been demonstrated in various in vivo and in vitro models for sulfur-containing compounds found in naturally occurring products. Here, we report the growth inhibitory and apoptosis-related effects of a newly developed highly purified sulfur (HPS) on immortalized human oral keratinocytes (IHOKs) and on oral cancer cells representing two stages of oral cancer (HN4, HN12) based on a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, Western blotting, cell cycle analysis, and nuclear staining. The purity of the sulfur preparation was verified by high-performance liquid chromatography. HPS inhibited the proliferation of immortalized and malignant oral keratinocytes in a dose- and time-dependent manner. FITC-annexin V staining, DNA fragmentation testing, and Hoechst 33258 staining revealed that HPS inhibited cell growth via apoptosis. HPS increased the sub-G1 cell cycle fraction, with decreased expression of cyclins D1, D2, and E and their activating partners cdk2, cdk4, and cdk6, and a concomitant induction of p53 and p21/WAF1. Furthermore, HPS treatment increased the cytosolic level of cytochrome c and resulted in caspase-3 activation; this effect was correlated with Bax up-regulation and Bcl-2 down-regulation. Thus, these data suggest that HPS is a potential candidate for anti-cancer therapy in oral cancer.
在亚洲,硫通常作为一种草药用于治疗炎症和癌症,并且在各种体内和体外模型中已证明天然产物中含硫化合物具有强大的化学预防作用。在此,我们基于3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法、蛋白质印迹法、细胞周期分析和细胞核染色,报告一种新开发的高纯度硫(HPS)对永生化人口腔角质形成细胞(IHOKs)以及代表口腔癌两个阶段的口腔癌细胞(HN4、HN12)的生长抑制和凋亡相关作用。通过高效液相色谱法验证了硫制剂的纯度。HPS以剂量和时间依赖性方式抑制永生化和恶性口腔角质形成细胞的增殖。FITC-膜联蛋白V染色、DNA片段化检测和Hoechst 33258染色显示,HPS通过凋亡抑制细胞生长。HPS增加了亚G1期细胞周期比例,同时细胞周期蛋白D1、D2和E及其激活伴侣细胞周期蛋白依赖性激酶2(cdk2)、细胞周期蛋白依赖性激酶4(cdk4)和细胞周期蛋白依赖性激酶6(cdk6)的表达降低,并伴随p53和p21/WAF1的诱导。此外,HPS处理增加了细胞色素c的胞质水平并导致半胱天冬酶-3激活;这种作用与Bax上调和Bcl-2下调相关。因此,这些数据表明HPS是口腔癌抗癌治疗的潜在候选物。