Shikonin Inhibites Migration and Invasion of Thyroid Cancer Cells by Downregulating DNMT1

被引:31
|
作者
Zhang, Yue [1 ]
Sun, Bin [2 ]
Huang, Zhi [3 ]
Zhao, Dai-wei [4 ]
Zeng, Qingfan [5 ]
机构
[1] Guizhou Prov Peoples Hosp, Dept Intervent Radiol, Guiyang, Guizhou, Peoples R China
[2] First Peoples Hosp Guiyang, Dept Intervent Radiol, Guiyang, Guizhou, Peoples R China
[3] Guizhou Med Univ, Affiliated Baiyun Hosp, Dept Intervent Radiol, Guiyang, Guizhou, Peoples R China
[4] Guizhou Med Univ, Affiliated Hosp 2, Dept Thyroid Surg, Kaili, Guizhou, Peoples R China
[5] Guizhou Med Univ, Affiliated Baiyun Hosp, Dept Anesthesiol, Guiyang, Guizhou, Peoples R China
来源
MEDICAL SCIENCE MONITOR | 2018年 / 24卷
关键词
Methylation; Parathyroid Neoplasms; PTEN Phosphohydrolase; TUMOR-SUPPRESSOR; TENSIN HOMOLOG; PROMOTER HYPERMETHYLATION; INDUCED APOPTOSIS; PTEN; GROWTH; DNA; PHOSPHATASE; BREAST; CARCINOMA;
D O I
10.12659/MSM.908381
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Shikonin is a component of Chinese herbal medicine. The aim of this study was to investigate the effects of shikonin on cell migration of papillary thyroid cancer cells of the TPC-1 cell line in vitro and expression levels of the phosphate and tensin homolog deleted on chromosome 10 (PTEN) and DNA methyltransferase 1 (DNMT1) genes. Material/Methods: The Cell Counting Kit-8 (CCK-8) assay was performed to evaluate the proliferation of TPC-1 papillary thyroid cancer cells, and the normal thyroid cells, HTori-3, in vitro. A transwell motility assay was used to analyze the migration of TPC-1 cells. Western blot was performed to determine the expression levels of PTEN and DNMT1 genes. A methylation-specific polymerase chain reaction (PCR) (MSP) assay was used to evaluate the methylation of PTEN. Results: Following treatment with shikonin, the cell survival rate of TPC-1 cells decreased in a dose-dependent manner; the inhibitory effects on HTori-3 cells were less marked. Shikonin inhibited TPC-1 cell migration and invasion in a dose-dependent manner. The methylation of PTEN was suppressed by shikonin, which also reduced the expression of DNMT1 in a dose-dependent manner, and increased the expression of PTEN. Overexpression of DNMT1 promoted the migration of TPC-1 cells and the methylation of PTEN. Levels of protein expression of PTEN in TPC-1 cells treated with shikonin decreased, and were increased by DNMT1 knockdown. Conclusions: Shikonin suppressed the expression of DNMT1, reduced PTEN gene methylation, and increased PTEN protein expression, leading to the inhibition of TPC-1 cell migration.
引用
收藏
页码:661 / 670
页数:10
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