Investigation of quercetin‐induced HepG2 cell apoptosis‐associated cellular biophysical alterations by atomic force microscopy. Issue 2 (14th July 2015)

• Record Type: Journal Article
• Authors: Pi, Jiang; Li, Baole; Tu, Lvying; Zhu, Haiyan; Jin, Hua; Yang, Fen; Bai, Haihua; Cai, Huaihong; Cai, Jiye
• Is Part Of: Scanning. Volume 38:Issue 2(2016:Mar./Apr.)
• Page Start: 100
• Page End: 112
• Publication Date: 2015-07-14
• Subjects: quercetin -- apoptosis -- atomic force microscopy -- biophysical property; Scanning electron microscopy -- Periodicals; 502.825
• DOI: 10.1002/sca.21245
• Languages: English
• ISSNs: 0161-0457

Abstract

Summary: Quercetin, a wildly distributed bioflavonoid, has been proved to possess excellent antitumor activity on hepatocellular carcinoma (HCC). In the present study, the biophysical properties of HepG2 cells were qualitatively and quantitatively determined using high resolution atomic force microscopy (AFM) to understand the anticancer effects of quercetin on HCC cells at nanoscale. The results showed that quercetin could induce severe apoptosis in HepG2 cells through arrest of cell cycle and disruption of mitochondria membrane potential. Additionally, the nuclei and F‐actin structures of HepG2 cells were destroyed by quercetin treatment as well. AFM morphological data showed some typical apoptotic characterization of HepG2 cells with increased particle size and roughness in the ultrastructure of cell surface upon quercetin treatment. As an important biophysical property of cells, the membrane stiffness of HepG2 cells was further quantified by AFM force measurements, which indicated that HepG2 cells became much stiffer after quercetin treatment. These results collectively suggest that quercetin can be served as a potential therapeutic agent for HCC, which not only extends our understanding of the anticancer effects of quercetin against HCC cells into nanoscale, but also highlights the applications of AFM for the investigation of anticancer drugs. SCANNING 38:100–112, 2016. © 2015 Wiley Periodicals, Inc.