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Riboflavin-Induced DNA Damage and Anticancer Activity in Breast Cancer Cells under Visible Light: A TD-DFT and Study. | LitMetric

AI Article Synopsis

  • Targeted treatments for breast cancer aim to minimize harm to healthy cells, and this study investigates riboflavin as a light-activated anticancer compound.
  • Using advanced calculations, researchers discovered that riboflavin transfers electronic charges from DNA, with significant activation under visible light.
  • Experiments on breast cancer cell lines showed that riboflavin effectively inhibited cell growth when exposed to light, while sparing normal cells, indicating its potential as a selective anticancer agent.

Article Abstract

Targeted treatments for breast cancer that minimize harm to healthy cells are highly sought after. Our study explores the potentiality of riboflavin as a targeted anticancer compound that can be activated by light irradiation. Here, we integrated time-dependent density functional theory (TD-DFT) calculations and an study under visible light. The TD-DFT calculations revealed that the electronic charge transferred from the DNA base to riboflavin, with the most significant excitation peak occurring within the visible light range. Guided by these insights, an study was conducted on the breast cancer cell lines MCF-7 and MDA-MB-231. The results revealed substantial growth inhibition in these cell lines when exposed to riboflavin under visible light, with no such impact observed in the absence of light exposure. Interestingly, riboflavin exhibited no/minimal growth-inhibitory effects on the normal cell line L929, irrespective of light conditions. Moreover, through EtBr displacement (-) and the TUNEL assay, it has been illustrated that, upon exposure to visible light, riboflavin can intercalate within DNA and induce DNA damage. In conclusion, under visible light conditions, riboflavin emerges as a promising candidate with a selective and effective potent anticancer agent against breast cancer while exerting a minimal influence on regular cellular activity.

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Source
http://dx.doi.org/10.1021/acs.jcim.4c01104DOI Listing

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