Department of Surgery, Changhua Christian Hospital, Changhua City, 50006, Taiwan.
Department of Radiation Oncology, Cancer Center, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, 80708, Taiwan.
Sci Rep. 2018 Feb 8;8(1):2672. doi: 10.1038/s41598-018-21065-x.
Shikonin is a naphthoquinone isolated from the dried root of Lithospermum erythrorhizon, an herb used in Chinese medicine. Although several studies have indicated that shikonin exhibits antitumor activity in breast cancer, the mechanism of action remains unclear. In the present study, we performed transcriptome analysis using RNA-seq and explored the mechanism of action of shikonin in regulating the growth of different types of breast cancer cells. The IC of shikonin on MCF-7, SKBR-3 and MDA-MB-231 cells were 10.3 μΜ, 15.0 μΜ, 15.0 μΜ respectively. Our results also demonstrated that shikonin arrests the progression of cell cycle and induces apoptosis in MDA-MB-231 cells. Using RNA-seq transcriptome analysis, we found 38 common genes that significantly express in different types of breast cancer cells under shikonin treatment. In particular, our results indicated that shikonin induces the expression of dual specificity phosphatase (DUSP)-1 and DUSP2 in both RNA and protein levels. In addition, shikonin also inhibits the phosphorylation of JNK and p38, the downstream signaling molecules of DUSP1 and DUSP2. Therefore, our results suggest that shikonin induces the expression of DUSP1 and DUSP2 which consequently switches off JNK and p38 MAPK pathways and causes cell cycle arrest and apoptosis in breast cancer cells.
紫草素是一种萘醌类化合物,从中药紫草的干燥根中分离得到。虽然有几项研究表明紫草素在乳腺癌中具有抗肿瘤活性,但作用机制尚不清楚。在本研究中,我们使用 RNA-seq 进行了转录组分析,探讨了紫草素调节不同类型乳腺癌细胞生长的作用机制。紫草素对 MCF-7、SKBR-3 和 MDA-MB-231 细胞的 IC 分别为 10.3 μM、15.0 μM 和 15.0 μM。我们的结果还表明,紫草素可以阻止 MDA-MB-231 细胞周期的进展并诱导细胞凋亡。使用 RNA-seq 转录组分析,我们发现 38 个共同基因在紫草素处理下在不同类型的乳腺癌细胞中显著表达。特别是,我们的结果表明,紫草素在 RNA 和蛋白质水平上诱导双特异性磷酸酶 (DUSP)-1 和 DUSP2 的表达。此外,紫草素还抑制 JNK 和 p38 的磷酸化,这是 DUSP1 和 DUSP2 的下游信号分子。因此,我们的结果表明,紫草素诱导 DUSP1 和 DUSP2 的表达,从而关闭 JNK 和 p38 MAPK 通路,并导致乳腺癌细胞周期停滞和凋亡。