Resveratrol: A potential challenger against gastric cancer

被引:104
作者
Zulueta, Aida [1 ]
Caretti, Anna [1 ]
Signorelli, Paola [1 ]
Ghidoni, Riccardo [1 ]
机构
[1] Univ Milan, San Paolo Hosp, Dept Hlth Sci, I-20142 Milan, Italy
关键词
Resveratrol; Polyphenols; Gastric cancer; Diet; Cell cycle; Apoptosis; CELL-CYCLE ARREST; NATURAL-PRODUCT PRESENT; PROTEIN-KINASE-C; HELICOBACTER-PYLORI; TRANS-RESVERATROL; GROWTH-INHIBITION; RED WINE; IN-VITRO; TISSUE DISTRIBUTION; LOW BIOAVAILABILITY;
D O I
10.3748/wjg.v21.i37.10636
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Gastric cancer (GC) is the fourth most common cancer and the second leading cause of cancer-related mortality in the world. Late diagnosis and classical therapeutic approaches such as surgery, chemotherapy and radiotherapy make this disease a still threatening tumor. Genetic asset, environmental stress, dietary habit and infections caused by Helicobacter pylori (H. pylori) are the major causes concurring to GC initiation. A common mechanism is induction of radicals resulting in gastric mucosal injury. A regular food intake of antioxidant and radical scavenging agents has been proposed to exert protection against tumorigenesis. Resveratrol belongs to the polyphenol flavonoids class of antioxidants produced by a restricted number of plants. Resveratrol exerts bactericidal activity against H. pylori and is a powerful antioxidant, thus acting as a tumor preventive agent. Resveratrol intracellular signaling results in growth arrest and apoptosis, so that it can be directed against tumor progression. Resveratrol therapeutic potential against GC initiation and progression are reviewed here.
引用
收藏
页码:10636 / 10643
页数:8
相关论文
共 84 条
[1]
Aggarwal BB, 2004, ANTICANCER RES, V24, P2783
[2]
Green tea constituent epigallocatechin-3-gallate and induction of apoptosis and cell cycle arrest in human carcinoma cells [J].
Ahmad, N ;
Feyes, DK ;
Nieminen, AL ;
Agarwal, R ;
Mukhtar, H .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (24) :1881-1886
[3]
[Anonymous], 2020, CA Cancer J Clin, DOI DOI 10.3322/CAAC.21590
[4]
Cyclodextrin-Based Nanosponges for Delivery of Resveratrol: In Vitro Characterisation, Stability, Cytotoxicity and Permeation Study [J].
Ansari, Khalid A. ;
Vavia, Pradeep R. ;
Trotta, Francesco ;
Cavalli, Roberta .
AAPS PHARMSCITECH, 2011, 12 (01) :279-286
[5]
trans-Resveratrol inhibits H2O2-induced adenocarcinoma gastric cells proliferation via inactivation of MEK1/2-ERK1/2-c-Jun signalling axis [J].
Aquilano, Katia ;
Baldelli, Sara ;
Rotilio, Giuseppe ;
Ciriolo, Maria Rosa .
BIOCHEMICAL PHARMACOLOGY, 2009, 77 (03) :337-347
[6]
Resveratrol regulates cellular PKC α and δ to inhibit growth and induce apoptosis in gastric cancer cells [J].
Atten, MJ ;
Godoy-Romero, E ;
Attar, BM ;
Milson, T ;
Zopel, M ;
Holian, O .
INVESTIGATIONAL NEW DRUGS, 2005, 23 (02) :111-119
[7]
Resveratrol-induced inactivation of human gastric adenocarcinoma cells through a protein kinase C-mediated mechanism [J].
Atten, MJ ;
Attar, BM ;
Milson, T ;
Holian, O .
BIOCHEMICAL PHARMACOLOGY, 2001, 62 (10) :1423-1432
[8]
Therapeutic potential of resveratrol:: the in vivo evidence [J].
Baur, Joseph A. ;
Sinclair, David A. .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (06) :493-506
[9]
Recent patterns in gastric cancer: A global overview [J].
Bertuccio, Paola ;
Chatenoud, Liliane ;
Levi, Fabio ;
Praud, Delphine ;
Ferlay, Jacques ;
Negri, Eva ;
Malvezzi, Matteo ;
La Vecchia, Carlo .
INTERNATIONAL JOURNAL OF CANCER, 2009, 125 (03) :666-673
[10]
Resveratrol induces SIRT1-and energy-stress-independent inhibition of tumor cell regrowth after low-dose platinum treatment [J].
Bjorklund, My ;
Roos, Jeanette ;
Gogvadze, Vladimir ;
Shoshan, Maria .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2011, 68 (06) :1459-1467