Unraveling the Anticancer Effect of Curcumin and Resveratrol

被引:86
作者
Pavan, Aline Renata [1 ]
Bernardes da Silva, Gabriel Dalio [1 ]
Jornada, Daniela Hartmann [1 ]
Chiba, Diego Eidy [1 ]
dos Santos Fernandes, Guilherme Felipe [1 ]
Chin, Chung Man [1 ]
dos Santos, Jean Leandro [1 ]
机构
[1] UNESP Univ Estadual Paulista, Sch Pharmaceut Sci, BR-14800903 Araraquara, Brazil
来源
NUTRIENTS | 2016年 / 8卷 / 11期
基金
巴西圣保罗研究基金会;
关键词
cancer; resveratrol; curcumin; polyphenols; anticancer; BREAST-CANCER CELLS; NF-KAPPA-B; EPITHELIAL-MESENCHYMAL TRANSITION; INDUCED MATRIX-METALLOPROTEINASE-9 EXPRESSION; MITOCHONDRIAL-MEMBRANE PERMEABILIZATION; INFLAMMATORY CYTOKINES CXCL1; CATENIN SIGNALING PATHWAY; LUNG ADENOCARCINOMA CELLS; ENDOTHELIAL GROWTH-FACTOR; INHIBITS TUMOR-GROWTH;
D O I
10.3390/nu8110628
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
Resveratrol and curcumin are natural products with important therapeutic properties useful to treat several human diseases, including cancer. In the last years, the number of studies describing the effect of both polyphenols against cancer has increased; however, the mechanism of action in all of those cases is not completely comprehended. The unspecific effect and the ability to interfere in assays by both polyphenols make this challenge even more difficult. Herein, we analyzed the anticancer activity of resveratrol and curcumin reported in the literature in the last 11 years, in order to unravel the molecular mechanism of action of both compounds. Molecular targets and cellular pathways will be described. Furthermore, we also discussed the ability of these natural products act as chemopreventive and its use in association with other anticancer drugs.
引用
收藏
页数:50
相关论文
共 450 条
  • [1] Tumour growth inhibition and anti-angiogenic effects using curcumin correspond to combined PDE2 and PDE4 inhibition
    Abusnina, Abdurazzag
    Keravis, Therese
    Zhou, Qingwei
    Justiniano, Helene
    Lobstein, Annelise
    Lugnier, Claire
    [J]. THROMBOSIS AND HAEMOSTASIS, 2015, 113 (02) : 319 - 328
  • [2] Anti-proliferative effect of curcumin on melanoma cells is mediated by PDE1A inhibition that regulates the epigenetic integrator UHRF1
    Abusnina, Abdurazzag
    Keravis, Therese
    Yougbare, Issaka
    Bronner, Christian
    Lugnier, Claire
    [J]. MOLECULAR NUTRITION & FOOD RESEARCH, 2011, 55 (11) : 1677 - 1689
  • [3] Regulation of apoptotic protease activating factor-1 oligomerization and apoptosis by the WD-40 repeat region
    Adrain, C
    Slee, EA
    Harte, MT
    Martin, SJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (30) : 20855 - 20860
  • [4] Nuclear factor-κ-B:: The enemy within
    Aggarwal, BB
    [J]. CANCER CELL, 2004, 6 (03) : 203 - 208
  • [5] Curcumin (diferuloylmethane) down-regulates expression of cell proliferation and antiapoptotic and metastatic gene products through suppression of IκBα kinase and Akt activation
    Aggarwal, S
    Ichikawa, H
    Takada, Y
    Sandur, SK
    Shishodia, S
    Aggarwal, BB
    [J]. MOLECULAR PHARMACOLOGY, 2006, 69 (01) : 195 - 206
  • [6] Protein kinase CK2 modulates apoptosis induced by resveratrol and epigallocatechin-3-gallate in prostate cancer cells
    Ahmad, Kashif A.
    Harris, Nathan H.
    Johnson, Andrew D.
    Lindvall, Hans C. N.
    Wang, Guixia
    Ahmed, Khalil
    [J]. MOLECULAR CANCER THERAPEUTICS, 2007, 6 (03) : 1006 - 1012
  • [7] Resveratrol-induced apoptosis in human breast cancer cells is mediated primarily through the caspase-3-dependent pathway
    Alkhalaf, Moussa
    El-Mowafy, Abdulla
    Renno, Waleed
    Rachid, Ousama
    Ali, Ahmed
    Al-Attyiah, Rajaa
    [J]. ARCHIVES OF MEDICAL RESEARCH, 2008, 39 (02) : 162 - 168
  • [8] Resveratrol-induced apoptosis is associated with activation of p53 and inhibition of protein translation in T47D human breast cancer cells
    Alkhalaf, Moussa
    [J]. PHARMACOLOGY, 2007, 80 (2-3) : 134 - 143
  • [9] Almhanna K, 2011, ANTICANCER RES, V31, P4387
  • [10] Protein tyrosine phosphatases in the human genome
    Alonso, A
    Sasin, J
    Bottini, N
    Friedberg, I
    Friedberg, I
    Osterman, A
    Godzik, A
    Hunter, T
    Dixon, J
    Mustelin, T
    [J]. CELL, 2004, 117 (06) : 699 - 711