Methanol extract of Sanguisorba officinalis L. with cytotoxic activity against PC3 human prostate cancer cells

被引:44
作者
Choi, Eun-Sun [1 ]
Kim, Jun-Sung [2 ]
Kwon, Ki-Han [3 ]
Kim, Hyng-Seop [4 ]
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 140200, South Korea
[3] Gwangju Univ, Dept Food Sci & Nutr, Coll Hlth Welf & Educ, Kwangju 503703, South Korea
[4] Chonbuk Natl Univ, Dept Oral Periodontol, Sch Dent, Inst Oral Biosci, Jeonju 561756, South Korea
基金
新加坡国家研究基金会;
关键词
Sanguisorba officinalis L; myeloid cell leukemia-1; Bax; oligomerization; prostate cancer; MCL-1; DOWN-REGULATION; TARGETING MCL-1; DEPENDENT APOPTOSIS; MEDIATED APOPTOSIS; BCL-2; BAX; PROTEIN; DEATH; MITOCHONDRIA; INDUCTION;
D O I
10.3892/mmr.2012.949
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sanguisorba officinalis is a natural plant that has been traditionally used for the treatment of inflammatory and metabolic diseases. Several studies have reported that its extracts exhibit anticancer, antioxidative and anti-lipid peroxidation activities. However, the effects of this plant on human prostate cancer cells have not yet been investigated. In the present study, we investigated the inhibitory effects and underlying mechanisms of a methanol extract of Sanguisorba officinalis (MESO) in PC3 human prostate cancer cells. MESO significantly decreased cell growth and induced apoptosis through the intrinsic apoptosis pathway. MESO decreased the expression levels of myeloid cell leukemia-1 (Mcl-1), a Bcl-2-like anti-apoptotic protein that is highly expressed in various cancer cell lines. Expression levels of the pro-apoptotic protein Bax were increased by MESO whereas those of Bak and Bcl-xL were unchanged. In addition, MESO induced the oligomerization of Bax in the mitochondrial outer membrane. These results suggest that MESO inhibits the growth of prostate cancer cells and induces apoptotic cell death by the downregulation of Mcl-1 protein expression and the oligomerization of Bax. Therefore, MESO has potential as a drug candidate for the treatment of prostate cancer.
引用
收藏
页码:670 / 674
页数:5
相关论文
共 42 条
  • [1] Bcl-2-regulated apoptosis: mechanism and therapeutic potential
    Adams, Jerry M.
    Cory, Suzanne
    [J]. CURRENT OPINION IN IMMUNOLOGY, 2007, 19 (05) : 488 - 496
  • [2] Ways of dying: multiple pathways to apoptosis
    Adams, JM
    [J]. GENES & DEVELOPMENT, 2003, 17 (20) : 2481 - 2495
  • [3] Mcl-1 is a potential therapeutic target in multiple types of cancer
    Akgul, C.
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2009, 66 (08) : 1326 - 1336
  • [4] Anti-inflammatory drugs, antioxidants, and prostate cancer prevention
    Bardia, Aditya
    Platz, Elizabeth A.
    Yegnasubramanian, Srinivasan
    De Marzo, Angelo M.
    Nelson, William G.
    [J]. CURRENT OPINION IN PHARMACOLOGY, 2009, 9 (04) : 419 - 426
  • [5] Camptothecin and khat (Catha edulis Forsk.) induced distinct cell death phenotypes involving modulation of c-FLIPL, Mcl-1, procaspase-8 and mitochondrial function in acute myeloid leukemia cell lines
    Bredholt, Therese
    Dimba, Elizabeth A. O.
    Hagland, Hanne R.
    Wergeland, Line
    Skavland, Jorn
    Fossan, Kjell O.
    Tronstad, Karl J.
    Johannessen, Anne C.
    Vintermyr, Olav K.
    Gjertsen, Bjorn T.
    [J]. MOLECULAR CANCER, 2009, 8
  • [6] Acquired Activation of the Akt/Cyclooxygenase-2/Mcl-1 Pathway Renders Lung Cancer Cells Resistant to Apoptosis
    Chen, Wenjie
    Bai, Lang
    Wang, Xia
    Xu, Shanling
    Belinsky, Steven A.
    Lin, Yong
    [J]. MOLECULAR PHARMACOLOGY, 2010, 77 (03) : 416 - 423
  • [7] Honokiol: a promising small molecular weight natural agent for the growth inhibition of oral squamous cell carcinoma cells
    Chen, Xi-rui
    Lu, Rui
    Dan, Hong-xia
    Liao, Ga
    Zhou, Min
    Li, Xiao-yu
    Ji, Ning
    [J]. INTERNATIONAL JOURNAL OF ORAL SCIENCE, 2011, 3 (01) : 34 - 42
  • [8] The inhibitory effect of triterpenoid glycosides originating from Sanguisorba officinalis on tissue factor activity and the production of TNF-α
    Cho, Jae Youl
    Yoo, Eun Sook
    Cha, Bae Cheon
    Park, Hwa-Jin
    Rhee, Man Hee
    Han, Yong Nam
    [J]. PLANTA MEDICA, 2006, 72 (14) : 1279 - 1284
  • [9] Regulation of Bax by c-Jun NH2-terminal kinase and Bcl-xL in vinblastine-induced apoptosis
    Chu, Rong
    Upreti, Meenakshi
    Ding, Wen-Xing
    Yin, Xiao-Ming
    Chambers, Timothy C.
    [J]. BIOCHEMICAL PHARMACOLOGY, 2009, 78 (03) : 241 - 248
  • [10] Chun Jae Yeon, 2010, Genes Cancer, V1, P868, DOI 10.1177/1947601910383416