Tian Ye, Zhen Liang, Bai Jian'an, Mei Yumei, Li Zheng, Lin Aihua, Li Xueliang
From the *Department of Gastroenterology, Nanjing Medical University; †Department of Gastroenterology, Affiliated Run Run Shaw Hospital of Nanjing Medical University; and ‡Department of Gastroenterology, Jiangsu Second Hospital of Traditional Chinese Medicine, Nanjing; and §Department of Intensive Care Unit, Affiliated SuQian Hospital of Drum Tower Hospital, SuQian, China.
Pancreas. 2017 Sep;46(8):1076-1081. doi: 10.1097/MPA.0000000000000895.
Baicalein is a Chinese traditional medicine that inhibits tumor migration and growth. Pancreatic neuroendocrine tumors (pNETs) have a high incidence in China, but there are still no effective treatments. The aim of our study was to investigate whether baicalein could inhibit pNETs.
In vitro, we used BON1-a cell line of pNETs-to analyze the apoptosis and migration and invasion after baicalein treatment via flow cytometry and Western blot. In vivo, we used a xenograft tumors model to evaluate the size of tumors after baicalein treatment. Western blot was used to analyze the expression of apoptosis and migration-related protein.
In vitro, the Cell Counting Kit 8 assay showed that baicalein decreased BON1 viability, and flow cytometry demonstrated that baicalein induced BON1 apoptosis and protein changes. In addition, baicalein inhibited BON1 migration and invasion as shown via a Transwell assay. In vivo, baicalein inhibited tumor growth and migration and also increased apoptosis-related protein expression.
Baicalein could increase caspase-3 and Bax expression and decrease survivin and Bcl-2 to induce apoptosis. It inhibits migration and invasion by decreasing expression of vascular endothelial growth factor and matrix metalloproteinases 2 and 9.
黄芩素是一种抑制肿瘤迁移和生长的中药。胰腺神经内分泌肿瘤(pNETs)在中国发病率较高,但仍无有效治疗方法。本研究旨在探讨黄芩素是否能抑制pNETs。
在体外,我们使用pNETs的BON1细胞系,通过流式细胞术和蛋白质免疫印迹法分析黄芩素处理后的细胞凋亡、迁移和侵袭情况。在体内,我们使用异种移植肿瘤模型评估黄芩素处理后肿瘤的大小。蛋白质免疫印迹法用于分析凋亡和迁移相关蛋白的表达。
在体外,细胞计数试剂盒8检测显示黄芩素降低了BON1细胞活力,流式细胞术表明黄芩素诱导了BON1细胞凋亡和蛋白变化。此外,通过Transwell实验表明黄芩素抑制了BON1细胞的迁移和侵袭。在体内,黄芩素抑制肿瘤生长和迁移,并增加凋亡相关蛋白表达。
黄芩素可增加半胱天冬酶-3和Bax表达,降低生存素和Bcl-2表达以诱导细胞凋亡。它通过降低血管内皮生长因子以及基质金属蛋白酶2和9的表达来抑制迁移和侵袭。