Inhibition of carcinogen induced c-Ha-ras and c-fos proto-oncogenes expression by dietary curcumin

Background: We investigated the chemopreventive action of dietary curcumin on 7,12-dimethylbenz(a)anthracene (DMBA)-initiated and 12,0-tetradecanoylphorbol-13-acetate (TPA)-promoted skin tumor formation in Swiss albino mice. Curcumin, a yellow coloring matter isolated from roots of Curcuma longa Lin...

Full description

Saved in:
Bibliographic Details
Main Authors: Limtrakul P.-N., Anuchapreeda S., Lipigorngoson S., Dunn F.W.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-3042652926&partnerID=40&md5=a52cf5e9a12fd23613660abe112d9b2c
http://www.ncbi.nlm.nih.gov/pubmed/11231886
http://cmuir.cmu.ac.th/handle/6653943832/2031
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
Language: English
id th-cmuir.6653943832-2031
record_format dspace
spelling th-cmuir.6653943832-20312014-08-30T02:00:24Z Inhibition of carcinogen induced c-Ha-ras and c-fos proto-oncogenes expression by dietary curcumin Limtrakul P.-N. Anuchapreeda S. Lipigorngoson S. Dunn F.W. Background: We investigated the chemopreventive action of dietary curcumin on 7,12-dimethylbenz(a)anthracene (DMBA)-initiated and 12,0-tetradecanoylphorbol-13-acetate (TPA)-promoted skin tumor formation in Swiss albino mice. Curcumin, a yellow coloring matter isolated from roots of Curcuma longa Linn, is a phenolic compound possessing antioxidant, free radical scavenger, and antiinflammatory properties. It has been shown by previously reported work that TPA-induced skin tumors were inhibited by topical application of curcumin, and curcumin has been shown to inhibit a variety of biological activities of TPA. Topical application of curcumin was reported to inhibit TPA-induced c-fos, c-jun and c-myc gene expression in mouse skin. This paper reports the effects of orally administered curcumin, which was consumed as a dietary component at concentrations of 0.2% or 1%, in ad libitum feeding. Results: A nimals i n which tumors had been initiated with DMBA and promoted with TPA experienced significantly fewer tumors and less tumor volume if they ingested either 0.2% or 1% curcumin diets. Also, the dietary consumption of curcumin resulted in a significantly decreased expression of ras and fos proto-oncogenes in the tumorous skin, as measured by enhanced chemiluminesence Western blotting detection system (Amersham). Conclusions: Whereas earlier work demonstrated that topical application of curcumin to mouse skin inhibited TPA-induced expression of c-fos, c-jun and c-myc oncogenes, our results are the first to show that orally consumed curcumin significantly inhibited DMBA- and TPA-induced ras and fos gene expression in mouse skin. © 2001 Limtrakul et al; licensee BioMed Central Ltd. 2014-08-30T02:00:24Z 2014-08-30T02:00:24Z 2001 Article 14712407 10.1186/1471-2407-1-1 11231886 BCMAC http://www.scopus.com/inward/record.url?eid=2-s2.0-3042652926&partnerID=40&md5=a52cf5e9a12fd23613660abe112d9b2c http://www.ncbi.nlm.nih.gov/pubmed/11231886 http://cmuir.cmu.ac.th/handle/6653943832/2031 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Background: We investigated the chemopreventive action of dietary curcumin on 7,12-dimethylbenz(a)anthracene (DMBA)-initiated and 12,0-tetradecanoylphorbol-13-acetate (TPA)-promoted skin tumor formation in Swiss albino mice. Curcumin, a yellow coloring matter isolated from roots of Curcuma longa Linn, is a phenolic compound possessing antioxidant, free radical scavenger, and antiinflammatory properties. It has been shown by previously reported work that TPA-induced skin tumors were inhibited by topical application of curcumin, and curcumin has been shown to inhibit a variety of biological activities of TPA. Topical application of curcumin was reported to inhibit TPA-induced c-fos, c-jun and c-myc gene expression in mouse skin. This paper reports the effects of orally administered curcumin, which was consumed as a dietary component at concentrations of 0.2% or 1%, in ad libitum feeding. Results: A nimals i n which tumors had been initiated with DMBA and promoted with TPA experienced significantly fewer tumors and less tumor volume if they ingested either 0.2% or 1% curcumin diets. Also, the dietary consumption of curcumin resulted in a significantly decreased expression of ras and fos proto-oncogenes in the tumorous skin, as measured by enhanced chemiluminesence Western blotting detection system (Amersham). Conclusions: Whereas earlier work demonstrated that topical application of curcumin to mouse skin inhibited TPA-induced expression of c-fos, c-jun and c-myc oncogenes, our results are the first to show that orally consumed curcumin significantly inhibited DMBA- and TPA-induced ras and fos gene expression in mouse skin. © 2001 Limtrakul et al; licensee BioMed Central Ltd.
format Article
author Limtrakul P.-N.
Anuchapreeda S.
Lipigorngoson S.
Dunn F.W.
spellingShingle Limtrakul P.-N.
Anuchapreeda S.
Lipigorngoson S.
Dunn F.W.
Inhibition of carcinogen induced c-Ha-ras and c-fos proto-oncogenes expression by dietary curcumin
author_facet Limtrakul P.-N.
Anuchapreeda S.
Lipigorngoson S.
Dunn F.W.
author_sort Limtrakul P.-N.
title Inhibition of carcinogen induced c-Ha-ras and c-fos proto-oncogenes expression by dietary curcumin
title_short Inhibition of carcinogen induced c-Ha-ras and c-fos proto-oncogenes expression by dietary curcumin
title_full Inhibition of carcinogen induced c-Ha-ras and c-fos proto-oncogenes expression by dietary curcumin
title_fullStr Inhibition of carcinogen induced c-Ha-ras and c-fos proto-oncogenes expression by dietary curcumin
title_full_unstemmed Inhibition of carcinogen induced c-Ha-ras and c-fos proto-oncogenes expression by dietary curcumin
title_sort inhibition of carcinogen induced c-ha-ras and c-fos proto-oncogenes expression by dietary curcumin
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-3042652926&partnerID=40&md5=a52cf5e9a12fd23613660abe112d9b2c
http://www.ncbi.nlm.nih.gov/pubmed/11231886
http://cmuir.cmu.ac.th/handle/6653943832/2031
_version_ 1681419781769527296