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A flavonoid-rich extract from bergamot juice prevents carcinogenesis in a genetic model of colorectal cancer, the Pirc rat (F344/NTac-Apcam1137).
Navarra, Michele; Femia, Angelo Pietro; Romagnoli, Andrea; Tortora, Katia; Luceri, Cristina; Cirmi, Santa; Ferlazzo, Nadia; Caderni, Giovanna.
Affiliation
  • Navarra M; Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, Italy. mnavarra@unime.it.
  • Femia AP; Section of Pharmacology and Toxicology, NEUROFARBA Department, University of Florence, Florence, Italy.
  • Romagnoli A; Section of Pharmacology and Toxicology, NEUROFARBA Department, University of Florence, Florence, Italy.
  • Tortora K; Section of Pharmacology and Toxicology, NEUROFARBA Department, University of Florence, Florence, Italy.
  • Luceri C; Section of Pharmacology and Toxicology, NEUROFARBA Department, University of Florence, Florence, Italy.
  • Cirmi S; Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, Italy.
  • Ferlazzo N; Fondazione "Prof. Antonio Imbesi", Messina, Italy.
  • Caderni G; Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, Italy.
Eur J Nutr ; 59(3): 885-894, 2020 Apr.
Article in En | MEDLINE | ID: mdl-30919084
ABSTRACT

PURPOSE:

To determine the potential of a flavonoid-rich extract from bergamot juice (BJe) to prevent colorectal carcinogenesis (CRC) in vivo. MAIN

METHODS:

Pirc rats (F344/NTac-Apcam1137), mutated in Apc, the key gene in CRC, were treated with two different doses of BJe (35 mg/kg or 70 mg/kg body weight, respectively) mixed in the diet for 12 weeks. Then, the entire intestine was surgically removed and dissected for histological, immunohistochemical and molecular analyses.

RESULTS:

Rats treated with BJe showed a significant dose-related reduction in the colon preneoplastic lesions mucin-depleted foci (MDF). Colon and small intestinal tumours were also significantly reduced in rats supplemented with 70 mg/kg of BJe. To elucidate the involved mechanisms, markers of inflammation and apoptosis were determined. Compared to controls, colon tumours from BJe 70 mg/kg-supplemented rats showed a significant down-regulation of inflammation-related genes (COX-2, iNOS, IL-1ß, IL-6 and IL-10 and Arginase 1). Moreover, in colon tumours from rats fed with 70 mg/kg BJe, apoptosis was significantly higher than in controls. Up-regulation of p53 and down-regulation of survivin and p21 genes was also observed.

CONCLUSIONS:

These data indicate a strong chemopreventive activity of BJe that, at least in part, is due to its pro-apoptotic and anti-inflammatory actions. This effect could be exploited as a strategy to prevent CRC in high-risk patients.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Flavonoids / Plant Extracts / Colorectal Neoplasms / Citrus / Fruit and Vegetable Juices Limits: Animals Language: En Journal: Eur J Nutr Journal subject: CIENCIAS DA NUTRICAO Year: 2020 Document type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Flavonoids / Plant Extracts / Colorectal Neoplasms / Citrus / Fruit and Vegetable Juices Limits: Animals Language: En Journal: Eur J Nutr Journal subject: CIENCIAS DA NUTRICAO Year: 2020 Document type: Article Affiliation country: Italy