Aspirin inhibits colon cancer cell and tumor growth and downregulates specificity protein (Sp) transcription factors.
Acetylsalicylic acid (aspirin) is highly effective for treating colon cancer patients postdiagnosis; however, the mechanisms of action of aspirin in colon cancer are not well defined. Aspirin and its major metabolite sodium salicylate induced apoptosis and decreased colon cancer cell growth and the...
Main Authors: | , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2012-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3482208?pdf=render |
_version_ | 1828425027485171712 |
---|---|
author | Satya Pathi Indira Jutooru Gayathri Chadalapaka Vijayalekshmi Nair Syng-Ook Lee Stephen Safe |
author_facet | Satya Pathi Indira Jutooru Gayathri Chadalapaka Vijayalekshmi Nair Syng-Ook Lee Stephen Safe |
author_sort | Satya Pathi |
collection | DOAJ |
description | Acetylsalicylic acid (aspirin) is highly effective for treating colon cancer patients postdiagnosis; however, the mechanisms of action of aspirin in colon cancer are not well defined. Aspirin and its major metabolite sodium salicylate induced apoptosis and decreased colon cancer cell growth and the sodium salt of aspirin also inhibited tumor growth in an athymic nude mouse xenograft model. Colon cancer cell growth inhibition was accompanied by downregulation of Sp1, Sp3 and Sp4 proteins and decreased expression of Sp-regulated gene products including bcl-2, survivin, VEGF, VEGFR1, cyclin D1, c-MET and p65 (NFκB). Moreover, we also showed by RNA interference that β-catenin, an important target of aspirin in some studies, is an Sp-regulated gene. Aspirin induced nuclear caspase-dependent cleavage of Sp1, Sp3 and Sp4 proteins and this response was related to sequestration of zinc ions since addition of zinc sulfate blocked aspirin-mediated apoptosis and repression of Sp proteins. The results demonstrate an important underlying mechanism of action of aspirin as an anticancer agent and, based on the rapid metabolism of aspirin to salicylate in humans and the high salicylate/aspirin ratios in serum, it is likely that the anticancer activity of aspirin is also due to the salicylate metabolite. |
first_indexed | 2024-12-10T16:26:32Z |
format | Article |
id | doaj.art-ec777d6376554127837fc2d9a174f8c7 |
institution | Directory Open Access Journal |
issn | 1932-6203 |
language | English |
last_indexed | 2024-12-10T16:26:32Z |
publishDate | 2012-01-01 |
publisher | Public Library of Science (PLoS) |
record_format | Article |
series | PLoS ONE |
spelling | doaj.art-ec777d6376554127837fc2d9a174f8c72022-12-22T01:41:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01710e4820810.1371/journal.pone.0048208Aspirin inhibits colon cancer cell and tumor growth and downregulates specificity protein (Sp) transcription factors.Satya PathiIndira JutooruGayathri ChadalapakaVijayalekshmi NairSyng-Ook LeeStephen SafeAcetylsalicylic acid (aspirin) is highly effective for treating colon cancer patients postdiagnosis; however, the mechanisms of action of aspirin in colon cancer are not well defined. Aspirin and its major metabolite sodium salicylate induced apoptosis and decreased colon cancer cell growth and the sodium salt of aspirin also inhibited tumor growth in an athymic nude mouse xenograft model. Colon cancer cell growth inhibition was accompanied by downregulation of Sp1, Sp3 and Sp4 proteins and decreased expression of Sp-regulated gene products including bcl-2, survivin, VEGF, VEGFR1, cyclin D1, c-MET and p65 (NFκB). Moreover, we also showed by RNA interference that β-catenin, an important target of aspirin in some studies, is an Sp-regulated gene. Aspirin induced nuclear caspase-dependent cleavage of Sp1, Sp3 and Sp4 proteins and this response was related to sequestration of zinc ions since addition of zinc sulfate blocked aspirin-mediated apoptosis and repression of Sp proteins. The results demonstrate an important underlying mechanism of action of aspirin as an anticancer agent and, based on the rapid metabolism of aspirin to salicylate in humans and the high salicylate/aspirin ratios in serum, it is likely that the anticancer activity of aspirin is also due to the salicylate metabolite.http://europepmc.org/articles/PMC3482208?pdf=render |
spellingShingle | Satya Pathi Indira Jutooru Gayathri Chadalapaka Vijayalekshmi Nair Syng-Ook Lee Stephen Safe Aspirin inhibits colon cancer cell and tumor growth and downregulates specificity protein (Sp) transcription factors. PLoS ONE |
title | Aspirin inhibits colon cancer cell and tumor growth and downregulates specificity protein (Sp) transcription factors. |
title_full | Aspirin inhibits colon cancer cell and tumor growth and downregulates specificity protein (Sp) transcription factors. |
title_fullStr | Aspirin inhibits colon cancer cell and tumor growth and downregulates specificity protein (Sp) transcription factors. |
title_full_unstemmed | Aspirin inhibits colon cancer cell and tumor growth and downregulates specificity protein (Sp) transcription factors. |
title_short | Aspirin inhibits colon cancer cell and tumor growth and downregulates specificity protein (Sp) transcription factors. |
title_sort | aspirin inhibits colon cancer cell and tumor growth and downregulates specificity protein sp transcription factors |
url | http://europepmc.org/articles/PMC3482208?pdf=render |
work_keys_str_mv | AT satyapathi aspirininhibitscoloncancercellandtumorgrowthanddownregulatesspecificityproteinsptranscriptionfactors AT indirajutooru aspirininhibitscoloncancercellandtumorgrowthanddownregulatesspecificityproteinsptranscriptionfactors AT gayathrichadalapaka aspirininhibitscoloncancercellandtumorgrowthanddownregulatesspecificityproteinsptranscriptionfactors AT vijayalekshminair aspirininhibitscoloncancercellandtumorgrowthanddownregulatesspecificityproteinsptranscriptionfactors AT syngooklee aspirininhibitscoloncancercellandtumorgrowthanddownregulatesspecificityproteinsptranscriptionfactors AT stephensafe aspirininhibitscoloncancercellandtumorgrowthanddownregulatesspecificityproteinsptranscriptionfactors |