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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
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Assessment of antioxidant/anticarcinogenic activity of plant extracts by a combination of molecular methods

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Author
Stagos, D.; Karaberis, E.; Kouretas, D.
Date
2005
Keyword
mitomycin C
DNA breakage
Salmonella typhimurium
Ames test
bleomycin
sister chromatid exchange
topoisomerase I
oxidative stress
mutagenicity
reactive oxygen species (ROS)
plant extracts
plant
phenolics
antioxidant
antimutagenicity
chemoprevention
anticancer
SALMONELLA-TYPHIMURIUM TA102
CHROMATID EXCHANGE FORMATION
DNA
TOPOISOMERASE-I
HUMAN CANCER-CELLS
MITOMYCIN-C
OXIDATIVE STRESS
DAMAGE
MECHANISMS
INHIBITION
CHEMOPREVENTION
Medicine, Research & Experimental
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Abstract
Cancer chemoprevention is considered to be a promising approach for cancer control, as it has been identified by both epidemiological and molecular studies that environmental factors are the major causes of cancer. Chemoprevention can be defined as the use of agents to prevent, inhibit or reverse the process of carcinogenesis. Several epidemiological studies have shown that fruits, vegetables and common beverages, as well as herbs and plants, are rich sources of chemopreventive compounds. In the present report, a battery of in vitro methods for the identification of chemopreventive agents are presented. These methods include: i) inhibition of bleomycin-induced mutations in Salmonella typhimurium TA102 cells, ii) inhibition of bleomycin-induced sister chromatid exchanges (SCEs) in human peripheral blood lymphocytes, iii) protection from mitomycin C-induced DNA strand breakage and iv) inhibition of topoisomerase I DNA relaxation. The first three methods are also used for the identification of agents which prevent reactive oxygen species (ROS)-mediated DNA damage.
URI
http://hdl.handle.net/11615/33328
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