School of Medical Laboratory Science and Biotechnology, College of Medical Science and Technology, Taipei Medical University, 250 Wuxing St., Taipei 11031, Taiwan, ROC.
Anticancer Res. 2013 Aug;33(8):3225-31.
15,16-Dihydrotanshinone I (DHTS) is a component of the traditional Chinese medicinal plant Salvia miltiorrhiza Bunge. In this study, DHTS at as low as 2.5 μg/ml concentration significantly inhibited proliferation of human benign (SW480) and malignant (SW620) colorectal cancer cells, as shown by 3-(4,5)-dimethylthiahiazo (-z-y1)-3,5-diphenytetrazoliumromide (MTT) and flow cytometric analysis. Activating transcription factor (ATF)-3, a basic leucine zipper-type transcription factor, was found to be predominantly up-regulated in DHTS-treated SW480 and SW620 cells. The up-regulation of ATF3 was blocked by a c-JUN N-terminal kinase (JNK) or p38 inhibitor. Overexpression of ATF3 resulted in a significant augmentation of DHTS-induced apoptosis of SW480 cells, but resistance to DHTS-induced apoptosis of SW620 cells. These results suggest that DHTS has a strong therapeutic or preventive potential against cancer. In addition, ATF3 has a dual role in DHTS-induced apoptosis, depending on the degree of malignancy of colorectal cancer.
15,16-二氢丹参酮 I(DHTS)是传统中药丹参的一种成分。在这项研究中,DHTS 在低至 2.5μg/ml 的浓度下就显著抑制了人良性(SW480)和恶性(SW620)结肠直肠癌细胞的增殖,这一点通过 3-(4,5)-二甲基噻唑 (-z-y1)-3,5-二苯基四氮唑溴盐(MTT)和流式细胞术分析得到证实。激活转录因子(ATF)-3,一种碱性亮氨酸拉链型转录因子,在 DHTS 处理的 SW480 和 SW620 细胞中被发现主要上调。DHTS 诱导的 ATF3 上调被 c-JUN N 末端激酶(JNK)或 p38 抑制剂阻断。ATF3 的过表达导致 DHTS 诱导的 SW480 细胞凋亡显著增强,但对 SW620 细胞凋亡的抵抗。这些结果表明,DHTS 对癌症具有很强的治疗或预防潜力。此外,ATF3 在 DHTS 诱导的细胞凋亡中具有双重作用,取决于结直肠癌细胞的恶性程度。