天津医药 ›› 2019, Vol. 47 ›› Issue (7): 696-699.doi: 10.11958/20181831

• 细胞与分子生物学 • 上一篇    下一篇

β-五没食子酰葡萄糖对胰腺癌细胞糖酵解及增殖的影响

陈喜娟,胡立娟,邱帅,杨静,谢俊木子,王丰   

  1. 1天津医科大学(邮编300070);2天津市南开医院中西医结合急腹症研究所
  • 收稿日期:2018-11-22 修回日期:2019-04-18 出版日期:2019-07-15 发布日期:2019-08-01
  • 通讯作者: 王丰 E-mail:fengwangpi@163.com

Effects of β-PGG on glycolysis and proliferation of pancreatic cancer cells

CHEN Xi-juan,HU Li-juan,QIU Shuai,YANG Jing,XIE Jun-mu-zi,WANG Feng   

  1. 1 Tianjin Medical University, Tianjin 300070, China; 2 The Institute of Integrative Medicine for Acute Abdominal Diseases, Nankai Hospital
  • Received:2018-11-22 Revised:2019-04-18 Published:2019-07-15 Online:2019-08-01

摘要: 目的 研究 β-五没食子酰葡萄糖(β-PGG)对人胰腺癌细胞糖酵解途径的影响及细胞生长的调节潜能。方法 用不同浓度的 β-PGG(0、5、25、50、100 μmol/L)处理人胰腺癌 MiaPaCa-2细胞,采用 CCK-8法检测 β-PGG对人胰腺癌MiaPaCa-2细胞的增殖作用,细胞化学试剂盒检测糖酵解的产物乳酸的生成,蛋白印迹法检测糖酵解的上游调节子缺氧诱导因子-1α(HIF-1α)和葡萄糖转运蛋白1(GLUT1)以及糖酵解酶己糖激酶-Ⅱ(HK-Ⅱ)和磷酸果糖激酶(PFK)的蛋白表达水平。结果 CCK-8结果显示,β-PGG可以抑制人胰腺癌 MiaPaCa-2细胞的增殖,其抑制作 用呈现出剂量和时间依赖性(P<0.05)。检测细胞上清液的乳酸发现,无论是在常氧或缺氧条件下,β-PGG均能抑制乳酸的生成(P<0.05)。与对照组相比,β-PGG能抑制 HIF-1α、GLUT1、HK-Ⅱ和 PFK的表达水平,且抑制作用随着β-PGG浓度的增高而增加(P<0.05)。结论 β-PGG可以抑制人胰腺癌细胞系MiaPaCa-2的糖酵解与增殖,其抑制作用可能与抑制MiaPaCa-2细胞中HIF-1α、GLUT1、HK-Ⅱ和PFK的蛋白表达有关。

关键词: 胰腺肿瘤, 肿瘤细胞, 培养的, 缺氧诱导因子1, α亚基, 糖酵解, 乳酸, 细胞增殖, β-五没食子酰葡萄糖

Abstract: Objective To study the effect of penta-O-galloyl-β-D-glucose (β-PGG) on the glycolysis and growth of human pancreatic cancer cells. Methods MiaPaCa-2 human pancreatic cancer cells were treated with different concentrations of β-PGG. The proliferation of MiaPaCa-2 was assessed by CCK8 method. Cytochemical kit was used to determine the product of glycolysis, lactate. Hypoxia inducible factor-1α (HIF-1α), glucose transporter 1 (GLUT1), the glycolytic enzymes of hexokinase Ⅱ (HK - Ⅱ) and phosphofructokinase (PFK) were determined by Western blot assay.Results The results of CCK8 assay showed that β-PGG inhibited the proliferation of pancreatic cancer MiaPaCa-2 cells in a dose - and time-dependent manner (P<0.05). β - PGG also inhibited the production of lactate in both normoxic and hypoxia conditions (P<0.05). Compared with the control group, β-PGG inhibited the expression of HIF-1α, GLUT1, HK-Ⅱ and PFK. And the inhibitory effect increased with the increased concentration of β-PGG (P<0.05). Conclusion β-PGG can inhibit the glycolysis pathway of human pancreatic cancer cell line MiaPaCa-2 and also inhibit the proliferation of MiaPaCa-2 cells. The inhibition may be achieved by inhibiting the expressions of HIF-1α, GLUT1, HK-Ⅱ and PFK in cancer cells.

Key words: pancreatic neoplasms, tumor cells, cultured, hypoxia-inducible factor 1, alpha subunit, glycolysis, lactic acid, cell proliferation, β-PGG