Folic Acid supplementary reduce the incidence of adenocarcinoma in a mouse model of colorectal cancer: microarray gene expression profile

<p>Abstract</p> <p>Background</p> <p>Whether Folic acid is a potential drug that may prevent the progression of colorectal carcinoma and when to use are important healthy issues we focus on. Our study is to examine the effect of folic acid on the development of the CRC...

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Main Authors: Lin Yan-Wei, Wang Ji-Lin, Chen Hui-Min, Zhang Yan-Jie, Rong-Lu, Ren Lin-Lin, Hong Jie, Fang Jing-Yuan
Format: Article
Language:English
Published: BMC 2011-12-01
Series:Journal of Experimental & Clinical Cancer Research
Online Access:http://www.jeccr.com/content/30/1/116
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spelling doaj-b67908b2b823405181c3a34b78a7118b2020-11-25T00:24:48ZengBMCJournal of Experimental & Clinical Cancer Research1756-99662011-12-0130111610.1186/1756-9966-30-116Folic Acid supplementary reduce the incidence of adenocarcinoma in a mouse model of colorectal cancer: microarray gene expression profileLin Yan-WeiWang Ji-LinChen Hui-MinZhang Yan-JieRong-LuRen Lin-LinHong JieFang Jing-Yuan<p>Abstract</p> <p>Background</p> <p>Whether Folic acid is a potential drug that may prevent the progression of colorectal carcinoma and when to use are important healthy issues we focus on. Our study is to examine the effect of folic acid on the development of the CRC and the optimal time folic acid should be provided in a mouse-ICR model induced by 1, 2-Dimethylhydrazine. Also, we investigated the gene expression profile of this model related to folic acid.</p> <p>Method</p> <p>Female ICR mouse (n = 130) were divided into 7 groups either with the treatment of 1, 2-Dimethylhydrazine (20 mg/kg bodyweight) weekly or folic acid (8 mg/kg bodyweight) twice a week for 12 or 24 weeks. Using a 4 × 44 K Agilent whole genome oligo microarray assay, different gene expression among groups (NS, DMH, FA2, FA3) were identified and selected genes were validated by real-time polymerase chain reaction.</p> <p>Results</p> <p>Animals with a supplementary of folic acid showed a significant decrease in the incidence, the maximum diameter and multiplicity of adenocarcinomas (<it>P </it>< 0.05). Furthermore, there were fewer adenomas or adenocarcinomas developed in the group of folic acid supplementation in pre-adenoma stage compared to group of post-adenoma stage. Meanwhile, about 1070 genes that were changed by 1, 2-Dimethylhydrazine can be reversed by folic acid and 172 differentially genes were identified between the groups of pre- and post- adenoma stage using microarray gene expression analysis.</p> <p>Conclusion</p> <p>Our study demonstrated that folic acid supplementary was significantly associated with the decrease risk of CRC. And the subgroup of providing folic acid without precancerous lesions was more effective than that with precancerous lesions.</p> http://www.jeccr.com/content/30/1/116
collection DOAJ
language English
format Article
sources DOAJ
author Lin Yan-Wei
Wang Ji-Lin
Chen Hui-Min
Zhang Yan-Jie
Rong-Lu
Ren Lin-Lin
Hong Jie
Fang Jing-Yuan
spellingShingle Lin Yan-Wei
Wang Ji-Lin
Chen Hui-Min
Zhang Yan-Jie
Rong-Lu
Ren Lin-Lin
Hong Jie
Fang Jing-Yuan
Folic Acid supplementary reduce the incidence of adenocarcinoma in a mouse model of colorectal cancer: microarray gene expression profile
Journal of Experimental & Clinical Cancer Research
author_facet Lin Yan-Wei
Wang Ji-Lin
Chen Hui-Min
Zhang Yan-Jie
Rong-Lu
Ren Lin-Lin
Hong Jie
Fang Jing-Yuan
author_sort Lin Yan-Wei
title Folic Acid supplementary reduce the incidence of adenocarcinoma in a mouse model of colorectal cancer: microarray gene expression profile
title_short Folic Acid supplementary reduce the incidence of adenocarcinoma in a mouse model of colorectal cancer: microarray gene expression profile
title_full Folic Acid supplementary reduce the incidence of adenocarcinoma in a mouse model of colorectal cancer: microarray gene expression profile
title_fullStr Folic Acid supplementary reduce the incidence of adenocarcinoma in a mouse model of colorectal cancer: microarray gene expression profile
title_full_unstemmed Folic Acid supplementary reduce the incidence of adenocarcinoma in a mouse model of colorectal cancer: microarray gene expression profile
title_sort folic acid supplementary reduce the incidence of adenocarcinoma in a mouse model of colorectal cancer: microarray gene expression profile
publisher BMC
series Journal of Experimental & Clinical Cancer Research
issn 1756-9966
publishDate 2011-12-01
description <p>Abstract</p> <p>Background</p> <p>Whether Folic acid is a potential drug that may prevent the progression of colorectal carcinoma and when to use are important healthy issues we focus on. Our study is to examine the effect of folic acid on the development of the CRC and the optimal time folic acid should be provided in a mouse-ICR model induced by 1, 2-Dimethylhydrazine. Also, we investigated the gene expression profile of this model related to folic acid.</p> <p>Method</p> <p>Female ICR mouse (n = 130) were divided into 7 groups either with the treatment of 1, 2-Dimethylhydrazine (20 mg/kg bodyweight) weekly or folic acid (8 mg/kg bodyweight) twice a week for 12 or 24 weeks. Using a 4 × 44 K Agilent whole genome oligo microarray assay, different gene expression among groups (NS, DMH, FA2, FA3) were identified and selected genes were validated by real-time polymerase chain reaction.</p> <p>Results</p> <p>Animals with a supplementary of folic acid showed a significant decrease in the incidence, the maximum diameter and multiplicity of adenocarcinomas (<it>P </it>< 0.05). Furthermore, there were fewer adenomas or adenocarcinomas developed in the group of folic acid supplementation in pre-adenoma stage compared to group of post-adenoma stage. Meanwhile, about 1070 genes that were changed by 1, 2-Dimethylhydrazine can be reversed by folic acid and 172 differentially genes were identified between the groups of pre- and post- adenoma stage using microarray gene expression analysis.</p> <p>Conclusion</p> <p>Our study demonstrated that folic acid supplementary was significantly associated with the decrease risk of CRC. And the subgroup of providing folic acid without precancerous lesions was more effective than that with precancerous lesions.</p>
url http://www.jeccr.com/content/30/1/116
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