Apoptotic effect of hot water extract of Sanguisorba officinalis L. in human oral cancer cells

被引:30
作者
Shin, Ji-Ae [1 ]
Kim, Jun-Sung [2 ]
Kwon, Ki-Han [3 ]
Nam, Jeong-Seok [4 ]
Jung, Ji-Youn [5 ]
Cho, Nam-Pyo [1 ]
Cho, Sung-Dae [1 ]
机构
[1] Chonbuk Natl Univ, Dept Oral Pathol, Sch Dent, Inst Oral Biosci, Jeonju 561756, South Korea
[2] Biterials Co Ltd, R&D Ctr, Seoul, South Korea
[3] Gwangju Univ, Dept Food Sci & Nutr, Coll Hlth Welf & Educ, Kwangju, South Korea
[4] Gachon Univ Med & Sci, Lee Gil Ya Canc & Diabet Inst, Inchon, South Korea
[5] Kongju Natl Univ, Dept Compan & Lab Anim Sci, Yesan, South Korea
基金
新加坡国家研究基金会;
关键词
Sanguisorba officinalis L; myeloid cell leukemia-1; specificity protein 1; oral cancer; apoptosis; MOLECULE BCL-2/BCL-X-L INHIBITOR; MULTIPLE-MYELOMA CELLS; DOWN-REGULATION; BAK ACTIVATION; BCL-2; FAMILY; MCL-1; EXPRESSION; ABT-737; RESISTANCE; LEUKEMIA;
D O I
10.3892/ol.2012.748
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sanguisorba officinalis L. has been used in traditional Asian medicine to treat diseases including diarrhea, chronic intestinal infections, duodenal ulcers and bleeding. This study examined the antiproliferative effects and apoptotic activity of hot water extract of S. officinalis L. (HESO) on HSC4 and HN22 human oral cancer cells. The effects of HESO were evaluated by the 3-(4,5-dimethylthiazol-20y1)(3-carboxymethoxyphenyl)-2-(4-sulphophenyl)-2H-tetrazolium (MTS) assay, 4'-6-diamidino-2-phenylindole (DAPI) staining and western blot analysis. HESO was found to inhibit cell growth and induce apoptosis in HSC4 and HN22 oral cancer cells. HESO downregulated myeloid cell leukemia-1 (Mcl-1) in HSC4 cells and was associated with the activation of Bak, resulting in Bak oligomerization on the mitochondrial outer membrane. HESO did not alter Mcl-1 expression in HN22 cells, but it decreased Sp1 expression. The downregulation of Sp1 by HESO in HN22 cells resulted in a decrease in survivin, a downstream target protein of Sp1. These results suggested that HESO inhibited the growth of oral cancer through either Mcl-1 or Sp1, indicating that HESO may serve as a potential drug candidate against oral cancer.
引用
收藏
页码:489 / 494
页数:6
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