Effects of food factors on signal transduction pathways
- 1 January 2000
- journal article
- review article
- Published by Wiley in BioFactors
- Vol. 12 (1-4) , 17-28
- https://doi.org/10.1002/biof.5520120104
Abstract
Consumption of plant‐derived foods, especially fruits and vegetables, has been linked to decreased risk of cancer. Laboratory studies with animals and cells in culture have shown cancer preventive activity of chemicals isolated from soy, tea, rice and many green, yellow and orange fruits and vegetables. Using cell culture, transgenic mice and knockout mice models to examine the anti‐cancer effects of these dietary factors at the molecular level, we found that (1) (‐)‐epigallocatechin gallate (EGCG), the major active polyphenol in green tea, and theaflavins, the major active components in black tea, inhibit epidermal growth factor (EGF)‐ or 12‐O‐tetradecanoylphorbol‐13‐acetate (TPA)‐induced JB6 cell transformation. At the same dose range that inhibited cell transformation, EGCG and theaflavins inhibited activator protein‐1 (AP‐1) activation. These compounds also inhibited ultraviolet B (UVB)‐induced AP‐1 and nuclear factor kappa B (NFκB)‐dependent transcriptional activation; (2) resveratrol, found at high levels in grapes, inhibited cell transformation through the induction of apoptosis, mediated through JNK and p53‐dependent pathways; (3) inositol hexaphosphate (InsP6), an active compound from rice and other grains, inhibited TPA‐ or EGF‐induced transformation and signal transduction through its effects on phosphatidylinositol‐3 kinase (PI‐3) kinase; (4) phenethyl isothiocyanate (PEITC), which occurs as a conjugate in certain cruciferous vegetables, inhibited cell transformation corresponding with the induction of apoptosis. An elevation of p53 is required for PEITC‐induced apoptosis. Our studies indicated that the chemopreventive effect of these food factors may be mediated by their effects on different signal transduction pathways; (5) retinoids (vitamin A and its metabolites) inhibited tumor promoter‐induced cell transformation and tumor promotion in transgenic mice through the inhibition of AP‐1 action but not through the activation of retinoic acid response element (RARE).Keywords
This publication has 42 references indexed in Scilit:
- JNK Activation Is Required for JB6 Cell Transformation Induced by Tumor Necrosis Factor-α but Not by 12-O-Tetradecanoylphorbol-13-AcetateJournal of Biological Chemistry, 1999
- The extracellular-signal-regulated protein kinases (Erks) are required for UV-induced AP-1 activation in JB6 cellsOncogene, 1999
- Increased synthesis of phosphocholine is required for UV-induced AP-1 activationOncogene, 1998
- IP6: A novel anti-cancer agentLife Sciences, 1997
- Phosphatidylinositol-3 Kinase Is Necessary for 12-O-Tetradecanoylphorbol-13-acetate-induced Cell Transformation and Activated Protein 1 ActivationJournal of Biological Chemistry, 1997
- Ultraviolet B-induced Activated Protein-1 Activation Does Not Require Epidermal Growth Factor Receptor but Is Blocked by a Dominant Negative PKCλ/ιJournal of Biological Chemistry, 1996
- Coactivator and Promoter-Selective Properties of RNA Polymerase I TAFsScience, 1995
- Studies of chemopreventive effects of myo-inositol on benzo(a)pyrene-induced neoplasia of the lung and forestomach of female A/J miceCarcinogenesis: Integrative Cancer Research, 1993
- Observation of inositol pentakis- and hexakis-phosphates in mammalian tissues by 31P NMRBiochemical and Biophysical Research Communications, 1987
- Responses of Preneoplastic Epidermal Cells to Tumor Promoters and Growth Factors: Use of Promoter-Resistant Variants for Mechanism StudiesJournal of Cellular Biochemistry, 1982