Repository of Research and Investigative Information

Repository of Research and Investigative Information

Shahid Sadoughi University of Medical Sciences

The inhibition of epidermal growth factor receptor signaling by hexagonal selenium nanoparticles modified by SiRNA

(2016) The inhibition of epidermal growth factor receptor signaling by hexagonal selenium nanoparticles modified by SiRNA. Cancer Gene Therapy. pp. 321-325.

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Official URL: https://www.scopus.com/inward/record.uri?eid=2-s2....

Abstract

The aim of this study was to investigate the effect of hexagonal selenium nanoparticles modified by SiRNA (HSNM-SiRNA) to inhibit epidermal growth factor receptor (EGFR) signaling in Human non-small-cell lung cancer (NSCLC). After synthesis, HSNM-SiRNA and HSNs were separately exposed to NSCLC cell lines (A549, H1299, H520, and H1975), and incubated for 6 h at 37 °C. Next, the expression of NFKB, MYC, STAT, ELK1, and GAPDH was evaluated by western blot and real-time PCR. The percentage of apoptotic cells and cell cycle progression were measured when exposed to HSNM-SiRNA and HSNs. Both western blot and real-time PCR results showed that HSNM-SiRNA could down-regulate the expression of all EGFR signaling genes. The percentage of apoptotic cells was significantly increased in all cell lines when exposed to HSNM-SiRNA (P>0.05). HSNM-SiRNA in A549 and H1299 cells significantly increased the proportion of cells in G1/G0 phase and significantly decreased the proportion of cells in S phase. © 2016 Nature America, Inc., part of Springer Nature.

Item Type: Article
Keywords: epidermal growth factor receptor; glyceraldehyde 3 phosphate dehydrogenase; hexagonal selenium nanoparticle; immunoglobulin enhancer binding protein; jun protein; Myc protein; nkiras1 protein; protein; protein fos; selenium nanoparticle; small interfering RNA; soat1 protein; STAT protein; transcription factor Elk 1; transcription factor Sp1; unclassified drug, apoptosis; Article; cell cycle G0 phase; cell cycle G1 phase; cell cycle progression; controlled study; down regulation; drug synthesis; human; human cell; non small cell lung cancer; priority journal; protein expression; quantitative structure activity relation; real time polymerase chain reaction; signal transduction; transmission electron microscopy; Western blotting
Page Range: pp. 321-325
Journal or Publication Title: Cancer Gene Therapy
Volume: 23
Number: 9
Publisher: Nature Publishing Group
Depositing User: ms soheila Bazm
URI: http://eprints.ssu.ac.ir/id/eprint/9796

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