Curcumin inhibits invasion and metastasis in the human ovarian cancer cells SKOV3 by CXCL12-CXCR4 axis

被引:0
|
作者
Mu Xiaoling [1 ]
Zhao Jing [2 ]
Xu Fang [3 ]
Tang Liangdan [1 ]
机构
[1] Chong Qing Med Univ, Affiliated Hosp 1, Dept Gynecol & Obstet, Chongqing 400016, Peoples R China
[2] Chong Qing Med Univ, Dept Pathophysiol, Chongqing 400016, Peoples R China
[3] Chong Qing Med Univ, Affiliated Hosp 1, Dept Emergence & ICU, Chongqing 400016, Peoples R China
来源
AFRICAN JOURNAL OF BIOTECHNOLOGY | 2010年 / 9卷 / 48期
关键词
Ovarian cancer; curcumin; invasion; metastasis; FACTOR-KAPPA-B; CXCR4; EXPRESSION; IN-VITRO; BONE-MARROW; GENE; VIVO;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Effects of curcumin on invasion and metastasis in the human ovarian cancer cells SKOV3 and approach if this inhibitory effects are related with CXCL12-CXCR4 axis were carefully studied. SKOV3 cells were treated with 10, 25, 50 mu mol/l curcumin for 24, 48 and 72 h. Proliferation of SKOV3 cells was measured with 3-(4,5-demethy-2-thiazolyl)-2,5-dephenyl-2H-tetrazolium-bromide (MTT) assay. Invasion and metastasis of SKOV3 cells were evaluated with transwell chamber. The expressions of CXCL-12 and CXCR4 were detected by western-blot. After being treated with curcumin, the proliferation of SKOV3 cells was inhibited in a time and dose-dependent manner (P < 0.05). In invasion assay, the number of cells in curcumin treated group to migrate to filter coated with Matrigel was reduced compared with the control group (P < 0.05). Meanwhile, in migration assay, the number of cells in curcumin treated group to migrate to filter was also decreased compared with the control group (P < 0.05). The expression level of CXCL-12 and CXCR4 were decreased. Our study indicated that curcumin could inhibit the invasion and metastasis of the human ovarian cancer cells SKOV3. Inhibiting the expression of CXCL-12 and CXCR4 was probably one of its molecular mechanisms.
引用
收藏
页码:8230 / 8234
页数:5
相关论文
共 50 条
  • [21] Role of the CXCL12-CXCR4 axis in the development of deep rectal endometriosis
    Leconte, M.
    Chouzenoux, S.
    Nicco, C.
    Chereau, C.
    Arkwright, S.
    Santulli, P.
    Weill, B.
    Chapron, C.
    Dousset, B.
    Batteux, F.
    JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2014, 103 : 45 - 52
  • [22] CXCR4, CXCL12 and the relative CXCL12-CXCR4 expression as prognostic factors in colon cancer
    Stanisavljevic, Luka
    Assmus, Jorg
    Storli, Kristian Eeg
    Leh, Sabine Maria
    Dahl, Olav
    Myklebust, Mette Pernille
    TUMOR BIOLOGY, 2016, 37 (06) : 7441 - 7452
  • [23] The CXCL12-CXCR4 Chemokine Pathway: A Novel Axis Regulates Lymphangiogenesis
    Zhuo, Wei
    Jia, Lin
    Song, Nan
    Lu, Xin-an
    Ding, Yanping
    Wang, Xiaofeng
    Song, Xiaomin
    Fu, Yan
    Luo, Yongzhang
    CLINICAL CANCER RESEARCH, 2012, 18 (19) : 5387 - 5398
  • [24] CXCL12-CXCR4 signalling axis confers gemcitabine resistance to pancreatic cancer cells: a novel target for therapy
    Singh, S.
    Srivastava, S. K.
    Bhardwaj, A.
    Owen, L. B.
    Singh, A. P.
    BRITISH JOURNAL OF CANCER, 2010, 103 (11) : 1671 - 1679
  • [25] Csk homologous kinase inhibits CXCL12-CXCR4 signaling in neuroblastoma
    Zagozdzon, Radoslaw
    Fu, Yigong
    Avraham, Hava Karsenty
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2008, 32 (03) : 619 - 623
  • [26] CXCL12-CXCR4 interactions modulate prostate cancer cell migration, metalloproteinase expression and invasion
    Singh, S
    Singh, UP
    Grizzle, WE
    Lillard, JW
    LABORATORY INVESTIGATION, 2004, 84 (12) : 1666 - 1676
  • [27] CXCL12/CXCR4 axis induces proliferation and invasion in human endometrial cancer
    Liu, Pingping
    Long, Ping
    Huang, Yu
    Sun, Fengyi
    Wang, Zhenyan
    AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH, 2016, 8 (04): : 1719 - 1729
  • [28] CXCL12-CXCR4/CXCR7 Axis in Colorectal Cancer: Therapeutic Target in Preclinical and Clinical Studies
    Khare, Tripti
    Bissonnette, Marc
    Khare, Sharad
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (14)
  • [29] The CXCL12-CXCR4/CXCR7 axis as a mechanism of immune resistance in gastrointestinal malignancies
    Daniel, Sara K.
    Seo, Y. David
    Pillarisetty, Venu G.
    SEMINARS IN CANCER BIOLOGY, 2020, 65 : 176 - 188
  • [30] Cancer associated fibroblasts stimulates cancer cell invasion through CXCL12-CXCR4 signaling in gastric cancer
    Izumi, Daisuke
    Ishimoto, Takatsugu
    Sugihara, Hietaka
    Sawayama, Hiroshi
    Karashima, Ryuichi
    Ida, Satoshi
    Imamura, Yu
    Iwagami, Shiro
    Baba, Yoshifumi
    Sakamoto, Yasuo
    Miyamoto, Yuji
    Yoshida, Naoya
    Baba, Hideo
    CANCER RESEARCH, 2014, 74 (19)