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The Molecular Effects of a High Fat Diet on Endometrial Tumour Biology

We sought to validate the BDII/Han rat model as a model for diet-induced obesity in endometrial cancer (EC) and determine if transcriptomic changes induced by a high fat diet (HFD) in an EC rat model can be used to identify novel biomarkers in human EC. Nineteen BDII/Han rats were included. Group A...

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Autores principales: Wilkinson, Michael, Sinclair, Piriyah, Dellatorre-Teixeira, Ludmilla, Swan, Patrick, Brennan, Eoin, Moran, Bruce, Wedekind, Dirk, Downey, Paul, Sheahan, Kieran, Conroy, Emer, Gallagher, William M., Docherty, Neil, le Roux, Carel, Brennan, Donal J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554710/
https://www.ncbi.nlm.nih.gov/pubmed/32927694
http://dx.doi.org/10.3390/life10090188
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author Wilkinson, Michael
Sinclair, Piriyah
Dellatorre-Teixeira, Ludmilla
Swan, Patrick
Brennan, Eoin
Moran, Bruce
Wedekind, Dirk
Downey, Paul
Sheahan, Kieran
Conroy, Emer
Gallagher, William M.
Docherty, Neil
le Roux, Carel
Brennan, Donal J.
author_facet Wilkinson, Michael
Sinclair, Piriyah
Dellatorre-Teixeira, Ludmilla
Swan, Patrick
Brennan, Eoin
Moran, Bruce
Wedekind, Dirk
Downey, Paul
Sheahan, Kieran
Conroy, Emer
Gallagher, William M.
Docherty, Neil
le Roux, Carel
Brennan, Donal J.
author_sort Wilkinson, Michael
collection PubMed
description We sought to validate the BDII/Han rat model as a model for diet-induced obesity in endometrial cancer (EC) and determine if transcriptomic changes induced by a high fat diet (HFD) in an EC rat model can be used to identify novel biomarkers in human EC. Nineteen BDII/Han rats were included. Group A (n = 7) were given ad lib access to a normal calorie, normal chow diet (NCD) while Group B (n = 12) were given ad lib access to a calorie rich HFD for 15 months. RNAseq was performed on endometrial tumours from both groups. The top-ranking differentially expressed genes (DEGs) were examined in the human EC using The Cancer Genome Atlas (TCGA) to assess if the BDII/Han rat model is an appropriate model for human obesity-induced carcinogenesis. Weight gain in HFD rats was double the weight gain of NCD rats (50 g vs. 25 g). The incidence of cancer was similar in both groups (4/7—57% vs. 4/12—33%; p = 0.37). All tumours were equivalent to a Stage 1A, Grade 2 human endometrioid carcinoma. A total of 368 DEGs were identified between the tumours in the HFD group compared to the NCD group. We identified two upstream regulators of the DEGs, mir-33 and Brd4, and a pathway analysis identified downstream enrichment of the colorectal cancer metastasis and ovarian cancer metastasis pathways. Top-ranking DEGs included Tex14, A2M, Hmgcs2, Adamts5, Pdk4, Crabp2, Capn12, Npw, Idi1 and Gpt. A2M expression was decreased in HFD tumours. Consistent with these findings, we found a significant negative correlation between A2M mRNA expression levels and BMI in the TCGA cohort (Spearman’s Rho = −0.263, p < 0.001). A2M expression was associated with improved overall survival (HR = 0.45, 95% CI 0.23–0.9, p = 0.024). Crabp2 expression was increased in HFD tumours. In human EC, CRABP2 expression was associated with reduced overall survival (HR = 3.554, 95% CI 1.875–6.753, p < 0.001). Diet-induced obesity can alter EC transcriptomic profiles. The BDII/Han rat model is a suitable model of diet-induced obesity in endometrial cancer and can be used to identify clinically relevant biomarkers in human EC.
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spelling pubmed-75547102020-10-19 The Molecular Effects of a High Fat Diet on Endometrial Tumour Biology Wilkinson, Michael Sinclair, Piriyah Dellatorre-Teixeira, Ludmilla Swan, Patrick Brennan, Eoin Moran, Bruce Wedekind, Dirk Downey, Paul Sheahan, Kieran Conroy, Emer Gallagher, William M. Docherty, Neil le Roux, Carel Brennan, Donal J. Life (Basel) Article We sought to validate the BDII/Han rat model as a model for diet-induced obesity in endometrial cancer (EC) and determine if transcriptomic changes induced by a high fat diet (HFD) in an EC rat model can be used to identify novel biomarkers in human EC. Nineteen BDII/Han rats were included. Group A (n = 7) were given ad lib access to a normal calorie, normal chow diet (NCD) while Group B (n = 12) were given ad lib access to a calorie rich HFD for 15 months. RNAseq was performed on endometrial tumours from both groups. The top-ranking differentially expressed genes (DEGs) were examined in the human EC using The Cancer Genome Atlas (TCGA) to assess if the BDII/Han rat model is an appropriate model for human obesity-induced carcinogenesis. Weight gain in HFD rats was double the weight gain of NCD rats (50 g vs. 25 g). The incidence of cancer was similar in both groups (4/7—57% vs. 4/12—33%; p = 0.37). All tumours were equivalent to a Stage 1A, Grade 2 human endometrioid carcinoma. A total of 368 DEGs were identified between the tumours in the HFD group compared to the NCD group. We identified two upstream regulators of the DEGs, mir-33 and Brd4, and a pathway analysis identified downstream enrichment of the colorectal cancer metastasis and ovarian cancer metastasis pathways. Top-ranking DEGs included Tex14, A2M, Hmgcs2, Adamts5, Pdk4, Crabp2, Capn12, Npw, Idi1 and Gpt. A2M expression was decreased in HFD tumours. Consistent with these findings, we found a significant negative correlation between A2M mRNA expression levels and BMI in the TCGA cohort (Spearman’s Rho = −0.263, p < 0.001). A2M expression was associated with improved overall survival (HR = 0.45, 95% CI 0.23–0.9, p = 0.024). Crabp2 expression was increased in HFD tumours. In human EC, CRABP2 expression was associated with reduced overall survival (HR = 3.554, 95% CI 1.875–6.753, p < 0.001). Diet-induced obesity can alter EC transcriptomic profiles. The BDII/Han rat model is a suitable model of diet-induced obesity in endometrial cancer and can be used to identify clinically relevant biomarkers in human EC. MDPI 2020-09-10 /pmc/articles/PMC7554710/ /pubmed/32927694 http://dx.doi.org/10.3390/life10090188 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wilkinson, Michael
Sinclair, Piriyah
Dellatorre-Teixeira, Ludmilla
Swan, Patrick
Brennan, Eoin
Moran, Bruce
Wedekind, Dirk
Downey, Paul
Sheahan, Kieran
Conroy, Emer
Gallagher, William M.
Docherty, Neil
le Roux, Carel
Brennan, Donal J.
The Molecular Effects of a High Fat Diet on Endometrial Tumour Biology
title The Molecular Effects of a High Fat Diet on Endometrial Tumour Biology
title_full The Molecular Effects of a High Fat Diet on Endometrial Tumour Biology
title_fullStr The Molecular Effects of a High Fat Diet on Endometrial Tumour Biology
title_full_unstemmed The Molecular Effects of a High Fat Diet on Endometrial Tumour Biology
title_short The Molecular Effects of a High Fat Diet on Endometrial Tumour Biology
title_sort molecular effects of a high fat diet on endometrial tumour biology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554710/
https://www.ncbi.nlm.nih.gov/pubmed/32927694
http://dx.doi.org/10.3390/life10090188
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