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Sodium salicylate and 5-aminosalicylic acid synergistically inhibit the growth of human colon cancer cells and mouse intestinal polyp-derived cells.
- Source :
-
Journal of clinical biochemistry and nutrition [J Clin Biochem Nutr] 2022 Mar; Vol. 70 (2), pp. 93-102. Date of Electronic Publication: 2021 Dec 18. - Publication Year :
- 2022
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Abstract
- As colon cancer is one of the most common cancers in the world, practical prevention strategies for colon cancer are needed. Recently, treatment with aspirin and/or 5-aminosalicylic acid-related agents was reported to reduce the number of intestinal polyps in patients with familial adenomatous polyposis. To evaluate the mechanism of aspirin and 5-aminosalicylic acid for suppressing the colon polyp growth, single and combined effects of 5-aminosalicylic acid and sodium salicylate (metabolite of aspirin) were tested in the two human colon cancer cells with different cyclooxygenase-2 expression levels and intestinal polyp-derived cells from familial adenomatous polyposis model mouse. The combination induced cell-cycle arrest at the G1 phase along with inhibition of cell growth and colony-forming ability in these cells. The combination reduced cyclin D1 via proteasomal degradation and activated retinoblastoma protein. The combination inhibited the colony-forming ability of mouse colonic mucosa cells by about 50% and the colony-forming ability of mouse intestinal polyp-derived cells by about 90%. The expression level of cyclin D1 in colon mucosa cells was lower than that in intestinal polyp-derived cells. These results suggest that this combination may be more effective in inhibiting cell growth of intestinal polyps through cyclin D1 down-regulation.<br />Competing Interests: No potential conflicts of interest were disclosed.<br /> (Copyright © 2022 JCBN.)
Details
- Language :
- English
- ISSN :
- 0912-0009
- Volume :
- 70
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of clinical biochemistry and nutrition
- Publication Type :
- Academic Journal
- Accession number :
- 35400827
- Full Text :
- https://doi.org/10.3164/jcbn.21-74