UMR 7213 CNRS, Laboratoire de Biophotonique et Pharmacologie, Université de Strasbourg, B.P. 60024, Illkirch, 67401, France.
Invest New Drugs. 2011 Apr;29(2):239-47. doi: 10.1007/s10637-009-9352-3. Epub 2009 Nov 27.
Cancer stem cells are expected to be responsible for tumor initiation and metastasis. These cells are therefore potential targets for innovative anticancer therapies. However, the absence of bona fide cancer stem cell lines is a real problem for the development of such approaches. Since teratocarcinoma cells are totipotent stem cells with a high degree of malignancy, we used them as a model of cancer stem cells in order to evaluate the anticancer chemopreventive activity of red wine polyphenols (RWPs) and to determine the underlying cellular and molecular mechanisms. We therefore investigated the effects of RWPs on the embryonal carcinoma (EC) cell line P19 which was grown in the same culture conditions as the most appropriate normal cell line counterpart, the pluripotent embryonic fibroblast cell line NIH/3T3. The present study indicates that RWPs selectively inhibited the proliferation of P19 EC cells and induced G1 cell cycle arrest in a dose-dependent manner. Moreover, RWPs treatment specifically triggered apoptosis of P19 EC cells in association with a dramatic upregulation of the tumor suppressor gene p53 and caspase-3 activation. Our findings suggest that the chemopreventive activity of RWPs on tumor initiation and development is related to a growth inhibition and a p53-dependent induction of apoptosis in teratocarcinoma cells. In addition, this study also shows that the EC cell line is a convenient source for studying the responses of cancer stem cells to new potential anticancer agents.
肿瘤干细胞被认为是肿瘤起始和转移的原因。因此,这些细胞是创新抗癌疗法的潜在靶点。然而,真正的肿瘤干细胞系的缺乏是此类方法发展的一个实际问题。由于畸胎癌细胞是具有高度恶性的全能干细胞,我们将其用作肿瘤干细胞的模型,以评估红葡萄酒多酚(RWPs)的抗癌化学预防活性,并确定潜在的细胞和分子机制。因此,我们研究了 RWPs 对胚胎癌细胞系 P19 的影响,该细胞系在与最合适的正常细胞系对应物多能胚胎成纤维细胞系 NIH/3T3 相同的培养条件下生长。本研究表明,RWPs 选择性地抑制 P19 EC 细胞的增殖,并以剂量依赖的方式诱导 G1 细胞周期停滞。此外,RWPs 处理特异性触发 P19 EC 细胞凋亡,与肿瘤抑制基因 p53 的显著上调和 caspase-3 的激活相关。我们的研究结果表明,RWPs 对肿瘤起始和发展的化学预防活性与畸胎癌细胞的生长抑制和 p53 依赖性诱导凋亡有关。此外,这项研究还表明,EC 细胞系是研究新的潜在抗癌药物对癌症干细胞反应的便捷来源。