Aras Aliye, Khokhar Abdur Rehman, Qureshi Muhammad Zahid, Silva Marcela Fernandes, Sobczak-Kupiec Agnieszka, Pineda Edgardo Alfonso Gomez, Hechenleitner Ana Adelina Winkler, Farooqi Ammad Ahmad
Department of Biology, Faculty of Science, Istanbul University, Istanbul, Turkey E-mail :
Asian Pac J Cancer Prev. 2014;15(9):3865-71. doi: 10.7314/apjcp.2014.15.9.3865.
It is becoming progressively more understandable that different phytochemicals isolated from edible plants interfere with specific stages of carcinogenesis. Cancer cells have evolved hallmark mechanisms to escape from death. Concordant with this approach, there is a disruption of spatiotemproal behaviour of signaling cascades in cancer cells, which can escape from apoptosis because of downregulation of tumor suppressor genes and over- expression of oncogenes. Genomic instability, intra-tumor heterogeneity, cellular plasticity and metastasizing potential of cancer cells all are related to molecular alterations. Data obtained through in vitro studies has convincingly revealed that curcumin, EGCG, resveratrol and quercetin are promising anticancer agents. Their efficacy has been tested in tumor xenografted mice and considerable experimental findings have stimulated researchers to further improve the bioavailability of these nutraceuticals. We partition this review into different sections with emphasis on how bioavailability of curcumin, EGCG, resveratrol and quercetin has improved using different nanotechnology approaches.
越来越容易理解的是,从可食用植物中分离出的不同植物化学物质会干扰致癌作用的特定阶段。癌细胞已经进化出逃避死亡的标志性机制。与此方法一致的是,癌细胞中信号级联的时空行为受到破坏,由于肿瘤抑制基因的下调和癌基因的过度表达,癌细胞可以逃避凋亡。癌细胞的基因组不稳定性、肿瘤内异质性、细胞可塑性和转移潜能都与分子改变有关。通过体外研究获得的数据令人信服地表明,姜黄素、表没食子儿茶素没食子酸酯(EGCG)、白藜芦醇和槲皮素是很有前景的抗癌剂。它们的疗效已在肿瘤异种移植小鼠中得到测试,大量的实验结果刺激研究人员进一步提高这些营养保健品的生物利用度。我们将本综述分为不同部分,重点关注如何使用不同的纳米技术方法提高姜黄素、EGCG、白藜芦醇和槲皮素的生物利用度。