alexa
Reach Us +441474556909
Zinc Oxide Nanoparticles Selectively Induce Apoptosis In Cancer Cells Mediated Through Reactive Oxygen Species | 6567
ISSN: 2157-7439

Journal of Nanomedicine & Nanotechnology
Open Access

Like us on:

OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Zinc oxide nanoparticles selectively induce apoptosis in cancer cells mediated through reactive oxygen species

International Conference and Exhibition on Nanotechnology & Nanomedicine

Maqusood Ahamed

ScientificTracks Abstracts: J Nanomedic Nanotechnol

DOI: 10.4172/2157-7439.S1.02

Abstract
Zinc oxide nanoparticles (ZnO NPs) are increasingly recognized for their utility in biological applications including biosensor and nanomedicine. It has been reported that ZnO NPs induce selective cytotoxicity to cancers cells. However, little is known about the toxicity mechanisms of ZnO NPs in cancer cells. This study was designed to investigate the possible mechanisms of apoptosis induced by ZnO NPs in human cancer cells. Cytotoxicity results showed that ZnO NPs have distinct effects on mammalian cell viability via killing cancer cells (A549, BEAS-2B and BALB 3T3) while posing no impact on normal rat astrocytes. To investigate the possible mechanisms of toxicity caused by ZnO NPs we have further utilized the human lung cancer cells (A549). ZnO NPs was found to induce reactive oxygen species (ROS) generation, oxidative stress and activities of caspase-3 & caspase-9 in a dose- and time dependent manner. Western blot results showed that ZnO NPs induced the expression of heat shock protein 70, a first-tier marker of cell damage and a cell-cycle checkpoint protein p53. Moreover, pro- apoptotic protein bax was up-regulated and the anti-apoptotic proteins, survivin and bcl- 2 were down-regulated in ZnO NPs exposed cells. In conclusion, our data demonstrates that ZnO nanorod induced apoptosis in human lung cancer cells through ROS and oxidative stress via p53, survivin, bax/bcl-2 and caspase pathways. Reference: Ahamed et al. 2011. Nanomedicine: Nanotechnology, Biology and Medicine. doi.org/10.1016/j. nano.2011.04.011
Biography
Maqusood Ahamed is an Assistant Professor of King Abdullah Institute for Nanotechnology at the King Saud University of Riyadh in Saudi Arabia. He received his Ph.D. degree from Hamdard University in 2007 and did his postdoctoral research (2007-2010) at University of Dayton, Ohio. Dr. Ahamed has authored more than 30 peer-reviewed articles and serves as reviewers for more than 20 journals.
Top