Resveratrol - From basic science to the clinic

被引:145
作者
Cucciolla, Valeria [1 ]
Borriello, Adriana [1 ]
Oliva, Adriana [1 ]
Galletti, Patrizia [1 ]
Zappia, Vincenzo [1 ]
Della Ragione, Fulvio [1 ]
机构
[1] Univ Naples 2, Dept Biochem & Biophys, I-80138 Naples, Italy
关键词
resveratrol; cell signaling; chemoprevention; cancer therapy; aging;
D O I
10.4161/cc.6.20.4815
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Plants produce an extraordinary array of low molecular mass natural products endowed with biological activity. Among these molecules, resveratrol (3,5,4'-trihydroxystilbene) has been identified as an inhibitor of carcinogenesis with a pleiotropic mode of action. Extensive literature on its anticancer activity, performed in cellular models, suggests a potential antiproliferative and apoptogenic use of the stilbene. Similarly, studies on implanted cancers and chemical-induced tumors confirm a potential chemotherapeutical interest of the compound. Moreover, recent intriguing studies have demonstrated, in mice, that the negative effects (insulin resistance and hyperglycemia) of a high-fat diet might be prevented by resveratrol treatment. Despite these promising observations, only few clinical trials have been performed on the compound due to the scarce interest of pharmaceutical industry. We suggest that resveratrol might be considered an interesting anticancer compound in association with more specific target-oriented drugs.
引用
收藏
页码:2495 / 2510
页数:16
相关论文
共 174 条
  • [1] Botanical antioxidants for chemoprevention of photocarcinogenesis
    Afaq, F
    Adhami, VM
    Ahmad, N
    Mukhtar, H
    [J]. FRONTIERS IN BIOSCIENCE-LANDMARK, 2002, 7 : D784 - D792
  • [2] Aggarwal BB, 2004, ANTICANCER RES, V24, P2783
  • [3] Hydrogen peroxide-mediated cytosolic acidification is a signal for mitochondrial translocation of Bax during drug-induced apoptosis of tumor cells
    Ahmad, KA
    Iskandar, KB
    Hirpara, JL
    Clement, MV
    Pervaiz, S
    [J]. CANCER RESEARCH, 2004, 64 (21) : 7867 - 7878
  • [4] Ahmad N, 2001, CLIN CANCER RES, V7, P1466
  • [5] Andlauer W, 2000, DRUG EXP CLIN RES, V26, P47
  • [6] Increased nuclear NAD biosynthesis and SIRT1 activation prevent axonal degeneration
    Araki, T
    Sasaki, Y
    Milbrandt, J
    [J]. SCIENCE, 2004, 305 (5686) : 1010 - 1013
  • [7] The p65 (RelA) subunit of NF-κB interacts with the histone deacetylase (HDAC) corepressors HDAC1 and HDAC2 to negatively regulate gene expression
    Ashburner, BP
    Westerheide, SD
    Baldwin, AS
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (20) : 7065 - 7077
  • [8] Resveratrol-induced inactivation of human gastric adenocarcinoma cells through a protein kinase C-mediated mechanism
    Atten, MJ
    Attar, BM
    Milson, T
    Holian, O
    [J]. BIOCHEMICAL PHARMACOLOGY, 2001, 62 (10) : 1423 - 1432
  • [9] Regioselective and stereospecific glucuronidation of trans- and cis-resveratrol in human
    Aumont, V
    Krisa, S
    Battaglia, E
    Netter, P
    Richard, T
    Mérillon, JM
    Magdalou, J
    Sabolovic, N
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2001, 393 (02) : 281 - 289
  • [10] Resveratrol enhances the expression of non-steroidal anti-inflammatory drug-activated gene (NAG-1) by increasing the expression of p53
    Baek, SJ
    Wilson, LC
    Eling, TE
    [J]. CARCINOGENESIS, 2002, 23 (03) : 425 - 434