Hydroxylated-Graphene Quantum Dots Induce DNA Damage and Disrupt Microtubule Structure in Human Esophageal Epithelial Cells

被引:32
作者
Li, Ming [1 ,2 ]
Gu, Meng-Meng [1 ,2 ]
Tian, Xin [1 ,2 ]
Xiao, Bei-Bei [1 ,2 ]
Lu, Siyuan [1 ,2 ]
Zhu, Wei [1 ,2 ]
Yu, Lan [3 ]
Shang, Zeng-Fu [1 ,2 ]
机构
[1] Soochow Univ, Med Coll, State Key Lab Radiat Med & Protect, Dept Radiobiol,Sch Radiat Med & Protect, 199 Renai Rd, Suzhou 215123, Peoples R China
[2] Soochow Univ, Jiangsu Higher Educ Inst, Collaborat Innovat Ctr Radiat Med, Suzhou 215123, Peoples R China
[3] Nanjing Med Univ, North Dist Suzhou Municipal Hosp, Affiliated Suzhou Hosp, Suzhou Digest Dis & Nutr Res Ctr, 242 Guangji Rd, Suzhou 215000, Peoples R China
基金
中国国家自然科学基金;
关键词
OH-GQDs; DNA damage; cell cycle regulation; microtubule structure; esophageal epithelial cells; CARBON NANOTUBES; PROTEIN-KINASE; IN-VITRO; CANCER; APOPTOSIS; TOXICITY; PATHWAY; REPLICATION; TRAFFICKING; INSTABILITY;
D O I
10.1093/toxsci/kfy090
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Graphene quantum dots (GQDs) have attracted significant interests due to their unique chemical and physical properties. In this study, we investigated the potential effects of hydroxyl-modified GQDs (OH-GQDs) on the human esophageal epithelial cell line HET-1A. Our data revealed significant cytotoxicity of OH-GQDs which decreased the viability of HET-1A in a dose and time-dependent manner. The moderate concentration (25 or 50 mu g/ml) of OH-GQDs significantly blocked HET-1A cells in G(0)/G(1) cell cycle phase. An increased percentage of gamma H2AX-positive and genomically unstable cells were also detected in cells treated with different doses of OH-GQDs (25, 50, and 100 mu g/ml). Microarray data revealed that OH-GQDs treatment down-regulated genes related to DNA damage repair, cell cycle regulation and cytoskeleton signal pathways indicating a novel role of OH-GQDs. Consistent with the microarray data, OH-GQDs disrupted microtubule structure and inhibited microtubule regrowth around centrosomes in HET-1A cells. In conclusion, our findings provide important evidence for considering the application of OH-GQDs in biomedical fields.
引用
收藏
页码:339 / 352
页数:14
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