TABLE 3.
S. No. | Molecular finding | References |
---|---|---|
I. | A reaction between polyphenols, Cu (II) and DNA results in DNA breakage in-vitro | Ahmad et al. (2000) |
Ahsan and Hadi (1998); Khan and Hadi (1998); Azam et al. (2004) | ||
Said Ahmad et al. (1992) | ||
II. | Polyphenol-Cu (II) system leads to DNA breakage in a cellular system | Azmi et al. (2005) |
III. | Polyphenols can mobilize endogenous copper ions from cells resulting in cellular DNA degradation | Azmi et al. (2006) |
Bhat et al. (2007) | ||
IV. | Nuclear copper is mobilized in the polyphenol induced oxidative cellular DNA degradation | Shamim et al. (2008) |
Ullah et al. (2009) | ||
V. | Oral administration of copper to rats results in enhanced prooxidant cellular DNA breakage by polyphenols | Khan et al. (2011) |
VI. | Diethylnitrosamine induced hepatocellular carcinoma in rats leads to increased prooxidant cellular DNA breakage by polyphenol (EGCG) | Farhan et al. (2015b) |
VII. | Polyphenols induce growth inhibition and apoptosis in malignant cells through copper redox-cycling and ROS generation | Ullah et al. (2011a) |
Khan et al. (2014) | ||
Zubair et al. (2016) | ||
VIII. | Supplementation with copper sensitizes normal breast epithelial cells to antiproliferative activity of polyphenols | Farhan et al. (2016) |
Khan et al. (2014) | ||
IX. | Silencing of copper transporter CTR1 desensitize normal breast epithelial cells in copper enriched medium to antiproliferative activity of polyphenol (EGCG) | Farhan et al. (2022) |