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Dietary restriction protects against diethylnitrosamine-induced hepatocellular tumorigenesis by restoring the disturbed gene expression profile

Hepatocellular carcinoma (HCC) is one of the most lethal and prevalent malignancies, worse still, there are very limited therapeutic measures with poor clinical outcomes. Dietary restriction (DR) has been known to inhibit spontaneous and induced tumors in several species, but the mechanisms are litt...

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Autores principales: Duan, Ting, Sun, Wenjie, Zhang, Mohan, Ge, Juan, He, Yansu, Zhang, Jun, Zheng, Yifan, Yang, Wei, Shen, Han-ming, Yang, Jun, Zhu, Xinqiang, Yu, Peilin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338348/
https://www.ncbi.nlm.nih.gov/pubmed/28262799
http://dx.doi.org/10.1038/srep43745
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author Duan, Ting
Sun, Wenjie
Zhang, Mohan
Ge, Juan
He, Yansu
Zhang, Jun
Zheng, Yifan
Yang, Wei
Shen, Han-ming
Yang, Jun
Zhu, Xinqiang
Yu, Peilin
author_facet Duan, Ting
Sun, Wenjie
Zhang, Mohan
Ge, Juan
He, Yansu
Zhang, Jun
Zheng, Yifan
Yang, Wei
Shen, Han-ming
Yang, Jun
Zhu, Xinqiang
Yu, Peilin
author_sort Duan, Ting
collection PubMed
description Hepatocellular carcinoma (HCC) is one of the most lethal and prevalent malignancies, worse still, there are very limited therapeutic measures with poor clinical outcomes. Dietary restriction (DR) has been known to inhibit spontaneous and induced tumors in several species, but the mechanisms are little known. In the current study, by using a diethylnitrosamine (DEN)-induced HCC mice model, we found that DR significantly reduced the hepatic tumor number and size, delayed tumor development, suppressed proliferation and promoted apoptosis. Further transcriptome sequencing of liver tissues from the DEN and the DEN accompanied with DR (DEN+DR) mice showed that DEN induced profound changes in the gene expression profile, especially in cancer-related pathways while DR treatment reversed most of the disturbed gene expression induced by DEN. Finally, transcription factor enrichment analysis uncovered the transcription factor specificity protein 1 (SP1) probably functioned as the main regulator of gene changes, orchestrating the protective effects of DR on DEN induced HCC. Taken together, by the first comprehensive transcriptome analysis, we elucidate that DR protects aginst DEN-induced HCC by restoring the disturbed gene expression profile, which holds the promise to provide effective molecular targets for cancer therapies.
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spelling pubmed-53383482017-03-08 Dietary restriction protects against diethylnitrosamine-induced hepatocellular tumorigenesis by restoring the disturbed gene expression profile Duan, Ting Sun, Wenjie Zhang, Mohan Ge, Juan He, Yansu Zhang, Jun Zheng, Yifan Yang, Wei Shen, Han-ming Yang, Jun Zhu, Xinqiang Yu, Peilin Sci Rep Article Hepatocellular carcinoma (HCC) is one of the most lethal and prevalent malignancies, worse still, there are very limited therapeutic measures with poor clinical outcomes. Dietary restriction (DR) has been known to inhibit spontaneous and induced tumors in several species, but the mechanisms are little known. In the current study, by using a diethylnitrosamine (DEN)-induced HCC mice model, we found that DR significantly reduced the hepatic tumor number and size, delayed tumor development, suppressed proliferation and promoted apoptosis. Further transcriptome sequencing of liver tissues from the DEN and the DEN accompanied with DR (DEN+DR) mice showed that DEN induced profound changes in the gene expression profile, especially in cancer-related pathways while DR treatment reversed most of the disturbed gene expression induced by DEN. Finally, transcription factor enrichment analysis uncovered the transcription factor specificity protein 1 (SP1) probably functioned as the main regulator of gene changes, orchestrating the protective effects of DR on DEN induced HCC. Taken together, by the first comprehensive transcriptome analysis, we elucidate that DR protects aginst DEN-induced HCC by restoring the disturbed gene expression profile, which holds the promise to provide effective molecular targets for cancer therapies. Nature Publishing Group 2017-03-06 /pmc/articles/PMC5338348/ /pubmed/28262799 http://dx.doi.org/10.1038/srep43745 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Duan, Ting
Sun, Wenjie
Zhang, Mohan
Ge, Juan
He, Yansu
Zhang, Jun
Zheng, Yifan
Yang, Wei
Shen, Han-ming
Yang, Jun
Zhu, Xinqiang
Yu, Peilin
Dietary restriction protects against diethylnitrosamine-induced hepatocellular tumorigenesis by restoring the disturbed gene expression profile
title Dietary restriction protects against diethylnitrosamine-induced hepatocellular tumorigenesis by restoring the disturbed gene expression profile
title_full Dietary restriction protects against diethylnitrosamine-induced hepatocellular tumorigenesis by restoring the disturbed gene expression profile
title_fullStr Dietary restriction protects against diethylnitrosamine-induced hepatocellular tumorigenesis by restoring the disturbed gene expression profile
title_full_unstemmed Dietary restriction protects against diethylnitrosamine-induced hepatocellular tumorigenesis by restoring the disturbed gene expression profile
title_short Dietary restriction protects against diethylnitrosamine-induced hepatocellular tumorigenesis by restoring the disturbed gene expression profile
title_sort dietary restriction protects against diethylnitrosamine-induced hepatocellular tumorigenesis by restoring the disturbed gene expression profile
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338348/
https://www.ncbi.nlm.nih.gov/pubmed/28262799
http://dx.doi.org/10.1038/srep43745
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