5-Aminosalicylic acid and olsalazine inhibit tumor growth in a rodent model of colorectal cancer

The ability of 5-aminosalicylic acid and olsalazine to inhibit colonic aberrant crypts and tumors was investigated in 1,2-dimethylhydrazine-treated rats. The effect of these drugs on the rates of tumor apoptosis and proliferation was studied as potential mechanisms for their action. 5-Aminosalicylic...

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Veröffentlicht in:Digestive diseases and sciences 2000-08, Vol.45 (8), p.1578-1584
Hauptverfasser: BROWN, Wendy A, FARMER, K. Chip, SKINNER, Stewart A, MALCONTENTI-WILSON, Caterina, MISAJON, Aileen, O'BRIEN, Paul E
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container_end_page 1584
container_issue 8
container_start_page 1578
container_title Digestive diseases and sciences
container_volume 45
creator BROWN, Wendy A
FARMER, K. Chip
SKINNER, Stewart A
MALCONTENTI-WILSON, Caterina
MISAJON, Aileen
O'BRIEN, Paul E
description The ability of 5-aminosalicylic acid and olsalazine to inhibit colonic aberrant crypts and tumors was investigated in 1,2-dimethylhydrazine-treated rats. The effect of these drugs on the rates of tumor apoptosis and proliferation was studied as potential mechanisms for their action. 5-Aminosalicylic acid reduced the number of aberrant crypt foci by over one third, while olsalazine had no effect on this parameter. However, both agents effectively reduced tumor number and load, increased the rate of tumor apoptosis, and reduced the rate of tumor cell proliferation. In conclusion, 5-aminosalicylic acid and olsalazine are both ultimately effective chemopreventive agents in this model; however, only 5-aminosalicylic acid inhibited the formation of aberrant crypt foci. The inhibitory effect of these agents in tumors is related to the inhibition of proliferation and the induction of apoptosis.
doi_str_mv 10.1023/A:1005517112039
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source Springer Nature - Complete Springer Journals
subjects Biological and medical sciences
Colorectal cancer
Digestive system
Medical sciences
Pharmacology. Drug treatments
title 5-Aminosalicylic acid and olsalazine inhibit tumor growth in a rodent model of colorectal cancer
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