The Timing and Duration of Folate Restriction Differentially Impacts Colon Carcinogenesis

Diet plays a crucial role in the development of colorectal cancer (CRC). Of particular importance, folate, present in foods and supplements, is a crucial modulator of CRC risk. The role of folate, and, specifically, the synthetic variant, folic acid, in the primary prevention of CRC has not been ful...

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Main Authors: Ali M. Fardous, Safa Beydoun, Andrew A. James, Hongzhi Ma, Diane C. Cabelof, Archana Unnikrishnan, Ahmad R. Heydari
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/14/1/16
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author Ali M. Fardous
Safa Beydoun
Andrew A. James
Hongzhi Ma
Diane C. Cabelof
Archana Unnikrishnan
Ahmad R. Heydari
author_facet Ali M. Fardous
Safa Beydoun
Andrew A. James
Hongzhi Ma
Diane C. Cabelof
Archana Unnikrishnan
Ahmad R. Heydari
author_sort Ali M. Fardous
collection DOAJ
description Diet plays a crucial role in the development of colorectal cancer (CRC). Of particular importance, folate, present in foods and supplements, is a crucial modulator of CRC risk. The role of folate, and, specifically, the synthetic variant, folic acid, in the primary prevention of CRC has not been fully elucidated. Animal studies varied considerably in the timing, duration, and supplementation of folates, leading to equivocal results. Our work attempts to isolate these variables to ascertain the role of folic acid in CRC initiation, as we previously demonstrated that folate restriction conferred protection against CRC initiation in a β-pol haploinsufficient mouse model. Here we demonstrated that prior adaptation to folate restriction altered the response to carcinogen exposure in wild-type C57BL/6 mice. Mice adapted to folate restriction for 8 weeks were protected from CRC initiation compared to mice placed on folate restriction for 1 week, irrespective of antibiotic supplementation. Through analyses of mTOR signaling, DNA methyltransferase, and DNA repair, we have identified factors that may play a critical role in the differential responses to folate restriction. Furthermore, the timing and duration of folate restriction altered these pathways differently in the absence of carcinogenic insult. These results represent novel findings, as we were able to show that, in the same model and under controlled conditions, folate restriction produced contrasting results depending on the timing and duration of the intervention.
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spelling doaj.art-a3152446136f45b6aadb0da670a53ff72023-11-23T12:02:52ZengMDPI AGNutrients2072-66432021-12-011411610.3390/nu14010016The Timing and Duration of Folate Restriction Differentially Impacts Colon CarcinogenesisAli M. Fardous0Safa Beydoun1Andrew A. James2Hongzhi Ma3Diane C. Cabelof4Archana Unnikrishnan5Ahmad R. Heydari6Department of Nutrition and Food Science, Wayne State University, Detroit, MI 48202, USADepartment of Nutrition and Food Science, Wayne State University, Detroit, MI 48202, USADepartment of Nutrition and Food Science, Wayne State University, Detroit, MI 48202, USADepartment of Nutrition and Food Science, Wayne State University, Detroit, MI 48202, USADepartment of Nutrition and Food Science, Wayne State University, Detroit, MI 48202, USADepartment of Biochemistry and Molecular Biology, University of Oklahoma Health and Science Center, Oklahoma City, OK 73104, USADepartment of Nutrition and Food Science, Wayne State University, Detroit, MI 48202, USADiet plays a crucial role in the development of colorectal cancer (CRC). Of particular importance, folate, present in foods and supplements, is a crucial modulator of CRC risk. The role of folate, and, specifically, the synthetic variant, folic acid, in the primary prevention of CRC has not been fully elucidated. Animal studies varied considerably in the timing, duration, and supplementation of folates, leading to equivocal results. Our work attempts to isolate these variables to ascertain the role of folic acid in CRC initiation, as we previously demonstrated that folate restriction conferred protection against CRC initiation in a β-pol haploinsufficient mouse model. Here we demonstrated that prior adaptation to folate restriction altered the response to carcinogen exposure in wild-type C57BL/6 mice. Mice adapted to folate restriction for 8 weeks were protected from CRC initiation compared to mice placed on folate restriction for 1 week, irrespective of antibiotic supplementation. Through analyses of mTOR signaling, DNA methyltransferase, and DNA repair, we have identified factors that may play a critical role in the differential responses to folate restriction. Furthermore, the timing and duration of folate restriction altered these pathways differently in the absence of carcinogenic insult. These results represent novel findings, as we were able to show that, in the same model and under controlled conditions, folate restriction produced contrasting results depending on the timing and duration of the intervention.https://www.mdpi.com/2072-6643/14/1/16folatefolic acidrestrictiondepletioncoloncancer
spellingShingle Ali M. Fardous
Safa Beydoun
Andrew A. James
Hongzhi Ma
Diane C. Cabelof
Archana Unnikrishnan
Ahmad R. Heydari
The Timing and Duration of Folate Restriction Differentially Impacts Colon Carcinogenesis
Nutrients
folate
folic acid
restriction
depletion
colon
cancer
title The Timing and Duration of Folate Restriction Differentially Impacts Colon Carcinogenesis
title_full The Timing and Duration of Folate Restriction Differentially Impacts Colon Carcinogenesis
title_fullStr The Timing and Duration of Folate Restriction Differentially Impacts Colon Carcinogenesis
title_full_unstemmed The Timing and Duration of Folate Restriction Differentially Impacts Colon Carcinogenesis
title_short The Timing and Duration of Folate Restriction Differentially Impacts Colon Carcinogenesis
title_sort timing and duration of folate restriction differentially impacts colon carcinogenesis
topic folate
folic acid
restriction
depletion
colon
cancer
url https://www.mdpi.com/2072-6643/14/1/16
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