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Activation of NF-E2 p45-related factor-2 transcription and inhibition of intestinal tumor development by AHCC, a standardized extract of cultured Lentinula edodes mycelia

It has been reported that activation of NF-E2 p45-related factor-2 (NRF2), a transcription factor, induces a variety of antioxidant enzymes, and plays an important role in preventing carcinogenesis. AHCC is a standardized extract of cultured Lentinula edodes mycelia and it has been demonstrated to i...

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Autores principales: Takahashi, Maiko, Fujii, Gen, Hamoya, Takahiro, Kurokawa, Yurie, Matsuzawa, Yui, Miki, Kohei, Komiya, Masami, Narita, Takumi, Mutoh, Michihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: the Society for Free Radical Research Japan 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877408/
https://www.ncbi.nlm.nih.gov/pubmed/31777421
http://dx.doi.org/10.3164/jcbn.19-36
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author Takahashi, Maiko
Fujii, Gen
Hamoya, Takahiro
Kurokawa, Yurie
Matsuzawa, Yui
Miki, Kohei
Komiya, Masami
Narita, Takumi
Mutoh, Michihiro
author_facet Takahashi, Maiko
Fujii, Gen
Hamoya, Takahiro
Kurokawa, Yurie
Matsuzawa, Yui
Miki, Kohei
Komiya, Masami
Narita, Takumi
Mutoh, Michihiro
author_sort Takahashi, Maiko
collection PubMed
description It has been reported that activation of NF-E2 p45-related factor-2 (NRF2), a transcription factor, induces a variety of antioxidant enzymes, and plays an important role in preventing carcinogenesis. AHCC is a standardized extract of cultured Lentinula edodes mycelia and it has been demonstrated to improve cancer. However, the effects of AHCC on NRF2 have not been examined, and the effects on intestinal adenoma development are not yet fully understood. We first investigated the effects of AHCC (1–5 mg/ml) on NRF2 activity in human colon cancer cell lines by a luciferase reporter gene assay, and found NRF2 transcriptional activities were increased ~12.6-fold. In addition, AHCC dose-dependently increased HO-1 and NQO-1 mRNA levels, and decreased interleukine-6 mRNA levels. Next, we administered 1,000 ppm AHCC for 8 weeks in the diet of Apc mutant Min mice, and found that AHCC significantly reduced the total number of intestinal polyps to 57.7% and to 67.6% of the control value in male and female Min mice, respectively, with suppression of interleukine-6 in the polyp part. These data suggest that AHCC possesses an ability to suppress cellular oxidative stress through activation of NRF2, thereby lowering intestinal polyp development in Min mice.
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spelling pubmed-68774082019-11-27 Activation of NF-E2 p45-related factor-2 transcription and inhibition of intestinal tumor development by AHCC, a standardized extract of cultured Lentinula edodes mycelia Takahashi, Maiko Fujii, Gen Hamoya, Takahiro Kurokawa, Yurie Matsuzawa, Yui Miki, Kohei Komiya, Masami Narita, Takumi Mutoh, Michihiro J Clin Biochem Nutr Original Article It has been reported that activation of NF-E2 p45-related factor-2 (NRF2), a transcription factor, induces a variety of antioxidant enzymes, and plays an important role in preventing carcinogenesis. AHCC is a standardized extract of cultured Lentinula edodes mycelia and it has been demonstrated to improve cancer. However, the effects of AHCC on NRF2 have not been examined, and the effects on intestinal adenoma development are not yet fully understood. We first investigated the effects of AHCC (1–5 mg/ml) on NRF2 activity in human colon cancer cell lines by a luciferase reporter gene assay, and found NRF2 transcriptional activities were increased ~12.6-fold. In addition, AHCC dose-dependently increased HO-1 and NQO-1 mRNA levels, and decreased interleukine-6 mRNA levels. Next, we administered 1,000 ppm AHCC for 8 weeks in the diet of Apc mutant Min mice, and found that AHCC significantly reduced the total number of intestinal polyps to 57.7% and to 67.6% of the control value in male and female Min mice, respectively, with suppression of interleukine-6 in the polyp part. These data suggest that AHCC possesses an ability to suppress cellular oxidative stress through activation of NRF2, thereby lowering intestinal polyp development in Min mice. the Society for Free Radical Research Japan 2019-11 2019-09-27 /pmc/articles/PMC6877408/ /pubmed/31777421 http://dx.doi.org/10.3164/jcbn.19-36 Text en Copyright © 2019 JCBN http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Takahashi, Maiko
Fujii, Gen
Hamoya, Takahiro
Kurokawa, Yurie
Matsuzawa, Yui
Miki, Kohei
Komiya, Masami
Narita, Takumi
Mutoh, Michihiro
Activation of NF-E2 p45-related factor-2 transcription and inhibition of intestinal tumor development by AHCC, a standardized extract of cultured Lentinula edodes mycelia
title Activation of NF-E2 p45-related factor-2 transcription and inhibition of intestinal tumor development by AHCC, a standardized extract of cultured Lentinula edodes mycelia
title_full Activation of NF-E2 p45-related factor-2 transcription and inhibition of intestinal tumor development by AHCC, a standardized extract of cultured Lentinula edodes mycelia
title_fullStr Activation of NF-E2 p45-related factor-2 transcription and inhibition of intestinal tumor development by AHCC, a standardized extract of cultured Lentinula edodes mycelia
title_full_unstemmed Activation of NF-E2 p45-related factor-2 transcription and inhibition of intestinal tumor development by AHCC, a standardized extract of cultured Lentinula edodes mycelia
title_short Activation of NF-E2 p45-related factor-2 transcription and inhibition of intestinal tumor development by AHCC, a standardized extract of cultured Lentinula edodes mycelia
title_sort activation of nf-e2 p45-related factor-2 transcription and inhibition of intestinal tumor development by ahcc, a standardized extract of cultured lentinula edodes mycelia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877408/
https://www.ncbi.nlm.nih.gov/pubmed/31777421
http://dx.doi.org/10.3164/jcbn.19-36
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