Anticancer Potential of Biogenic Silver Nanoparticles: A Mechanistic Study

• Published in: Pharmaceutics 2021-05, Vol.13 (5), p.707
• Main Authors: Khan, Mohd Shahnawaz, Alomari, Alya, Tabrez, Shams, Hassan, Iftekhar, Wahab, Rizwan, Bhat, Sheraz Ahmad, Alafaleq, Nouf Omar, Altwaijry, Nojood, Shaik, Gouse M., Zaidi, Syed Kashif, Nouh, Wessam, Alokail, Majed S., Ismael, Mohamed A.
• Format: Article
• Language: English
• Subjects: Biosynthesis; Breast cancer; Cancer therapies; Cell adhesion & migration; Cytotoxicity; Experiments; Gene expression; Infections; Medical research; Microscopy; Morphology; Nanomaterials; Nanoparticles; ROS; RT-PCR; scratch assay; silver nanoparticles; Spectrum analysis
• ISSN: 1999-4923; 1999-4923
• DOI: 10.3390/pharmaceutics13050707

The continuous loss of human life due to the paucity of effective drugs against different forms of cancer demands a better/noble therapeutic approach. One possible way could be the use of nanostructures-based treatment methods. In the current piece of work, we have synthesized silver nanoparticles (AgNPs) using plant (Heliotropiumbacciferum) extract using AgNO3 as starting materials. The size, shape, and structure of synthesized AgNPs were confirmed by various spectroscopy and microscopic techniques. The average size of biosynthesized AgNPs was found to be in the range of 15 nm. The anticancer potential of these AgNPs was evaluated by a battery of tests such as MTT, scratch, and comet assays in breast (MCF-7) and colorectal (HCT-116) cancer models. The toxicity of AgNPs towards cancer cells was confirmed by the expression pattern of apoptotic (p53, Bax, caspase-3) and antiapoptotic (BCl-2) genes by RT-PCR. The cell viability assay showed an IC50 value of 5.44 and 9.54 µg/mL for AgNPs in MCF-7 and HCT-116 cell lines respectively. We also observed cell migration inhibiting potential of AgNPs in a concentration-dependent manner in MCF-7 cell lines. A tremendous rise (150–250%) in the production of ROS was observed as a result of AgNPs treatment compared with control. Moreover, the RT-PCR results indicated the difference in expression levels of pro/antiapoptotic proteins in both cancer cells. All these results indicate that cell death observed by us is mediated by ROS production, which might have altered the cellular redox status. Collectively, we report the antimetastasis potential of biogenic synthesized AgNPs against breast and colorectal cancers. The biogenic synthesis of AgNPs seems to be a promising anticancer therapy with greater efficacy against the studied cell lines.