Combined ginger extract & Gelam honey modulate Ras/ERK and PI3K/AKT pathway genes in colon cancer HT29 cells

被引:77
作者
Tahir, Analhuda Abdullah [1 ]
Sani, Nur Fathiah Abdul [1 ]
Murad, Noor Azian [2 ]
Makpol, Suzana [1 ]
Ngah, Wan Zurinah Wan [1 ]
Yusof, Yasmin Anum Mohd [1 ]
机构
[1] Univ Kebangsaan Malaysia, Fac Med, Dept Biochem, Kuala Lumpur 56000, Malaysia
[2] Univ Teknol Malaysia, CLEAR, Kuala Lumpur 50480, Malaysia
关键词
Ginger; Gelam honey; HT29 colon cancer cells; Ras/ERK and PI3K/AKT pathways; TUALANG HONEY; APOPTOSIS; PROLIFERATION; DEATH; CHEMOPREVENTION; ANTICANCER; INHIBITORS; CARCINOMA; INDUCERS;
D O I
10.1186/s12937-015-0015-2
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: The interconnected Ras/ERK and PI3K/AKT pathways play a central role in colorectal tumorigenesis, and they are targets for elucidating mechanisms involved in attempts to induce colon cancer cell death. Both ginger (Zingiber officinale) and honey have been shown to exhibit anti-tumor and anti-inflammation properties against many types of cancer, including colorectal cancer. However, there are currently no reports showing the combined effect of these two dietary compounds in cancer growth inhibition. The aim of this study was to evaluate the synergistic effect of crude ginger extract and Gelam honey in combination as potential cancer chemopreventive agents against the colorectal cancer cell line HT29. Methods: The cells were divided into 4 groups: the first group represents HT29 cells without treatment, the second and third groups were cells treated singly with either ginger or Gelam honey, respectively, and the last group represents cells treated with ginger and Gelam honey combined. Results: The results of MTS assay showed that the IC50 of ginger and Gelam honey alone were 5.2 mg/ml and 80 mg/ml, respectively, whereas the IC50 of the combination treatment was 3 mg/ml of ginger plus 27 mg/ml of Gelam honey with a combination index of < 1, suggesting synergism. Cell death in response to the combined ginger and Gelam honey treatment was associated with the stimulation of early apoptosis (upregulation of caspase 9 and I.B genes) accompanied by downregulation of the KRAS, ERK, AKT, Bcl-xL, NFkB (p65) genes in a synergistic manner. Conclusions: In conclusion, the combination of ginger and Gelam honey may be an effective chemopreventive and therapeutic strategy for inducing the death of colon cancer cells.
引用
收藏
页数:10
相关论文
共 47 条
  • [31] A combination of indol-3-carbinol and genistein synergistically induces apoptosis in human colon cancer HT-29 cells by inhibiting Akt phosphorylation and progression of autophagy
    Nakamura, Yoshitaka
    Yogosawa, Shingo
    Izutani, Yasuyuki
    Watanabe, Hirotsuna
    Otsuji, Eigo
    Sakai, Tosiyuki
    [J]. MOLECULAR CANCER, 2009, 8
  • [32] [6]-Gingerol induces reactive oxygen species regulated mitochondrial cell death pathway in human epidermoid carcinoma A431 cells
    Nigam, Nidhi
    Bhui, Kulpreet
    Prasad, Sahdeo
    George, Jasmine
    Shukla, Yogeshwer
    [J]. CHEMICO-BIOLOGICAL INTERACTIONS, 2009, 181 (01) : 77 - 84
  • [33] Omar Z.A., 2011, National Cancer Registry Report 2007 Malaysian Cancer Statistics
  • [34] Pancione M, 2012, PATHOL RES INT, V2012, P11
  • [35] Synergistic Effect of Garcinol and Curcumin on Antiproliferative and Apoptotic Activity in Pancreatic Cancer Cells
    Parasramka, Mansi A.
    Gupta, Smiti Vaid
    [J]. JOURNAL OF ONCOLOGY, 2012, 2012
  • [36] Ginger inhibits cell growth and modulates angiogenic factors in ovarian cancer cells
    Rhode J.
    Fogoros S.
    Zick S.
    Wahl H.
    Griffith K.A.
    Huang J.
    Rebecca J.R.
    [J]. BMC Complementary and Alternative Medicine, 7 (1):
  • [37] Sak Katrin, 2012, Chemother Res Pract, V2012, P282570, DOI 10.1155/2012/282570
  • [38] Shailah Abdullah Shailah Abdullah, 2010, African Journal of Biochemistry Research, V4, P134
  • [39] Cancer chemoprevention with dietary phytochemicals
    Surh, YJ
    [J]. NATURE REVIEWS CANCER, 2003, 3 (10) : 768 - 780
  • [40] Synergistic effects of multiple natural products in pancreatic cancer cells
    Wang, Zhiwei
    Desmoulin, Sita
    Banerjee, Sanjeev
    Kong, Dejuan
    Li, Yiwei
    Deraniyagala, Rohan L.
    Abbruzzese, James
    Sarkar, Fazlul H.
    [J]. LIFE SCIENCES, 2008, 83 (7-8) : 293 - 300