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Sex Differences in Colon Cancer Metabolism Reveal A Novel Subphenotype
Women have a lower incidence of colorectal cancer (CRC) than men, however, they have a higher incidence of right-sided colon cancer (RCC). This is of concern as patients with RCC have the poorest clinical outcomes among all CRC patients. Aberrant metabolism is a known hallmark and therapeutic target...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078199/ https://www.ncbi.nlm.nih.gov/pubmed/32184446 http://dx.doi.org/10.1038/s41598-020-61851-0 |
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author | Cai, Yuping Rattray, Nicholas J. W. Zhang, Qian Mironova, Varvara Santos-Neto, Alvaro Hsu, Kuo-Shun Rattray, Zahra Cross, Justin R. Zhang, Yawei Paty, Philip B. Khan, Sajid A. Johnson, Caroline H. |
author_facet | Cai, Yuping Rattray, Nicholas J. W. Zhang, Qian Mironova, Varvara Santos-Neto, Alvaro Hsu, Kuo-Shun Rattray, Zahra Cross, Justin R. Zhang, Yawei Paty, Philip B. Khan, Sajid A. Johnson, Caroline H. |
author_sort | Cai, Yuping |
collection | PubMed |
description | Women have a lower incidence of colorectal cancer (CRC) than men, however, they have a higher incidence of right-sided colon cancer (RCC). This is of concern as patients with RCC have the poorest clinical outcomes among all CRC patients. Aberrant metabolism is a known hallmark and therapeutic target for cancer. We propose that metabolic subphenotypes exist between CRCs due to intertumoral molecular and genomic variation, and differences in environmental milieu of the colon which vary between the sexes. Metabolomics analysis of patient colon tumors (n = 197) and normal tissues (n = 39) revealed sex-specific metabolic subphenotypes dependent on anatomic location. Tumors from women with RCC were nutrient-deplete, showing enhanced energy production to fuel asparagine synthesis and amino acid uptake. The clinical importance of our findings were further investigated in an independent data set from The Cancer Genomic Atlas, and demonstrated that high asparagine synthetase (ASNS) expression correlated with poorer survival for women. This is the first study to show a unique, nutrient-deplete metabolic subphenotype in women with RCC, with implications for tumor progression and outcomes in CRC patients. |
format | Online Article Text |
id | pubmed-7078199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70781992020-03-23 Sex Differences in Colon Cancer Metabolism Reveal A Novel Subphenotype Cai, Yuping Rattray, Nicholas J. W. Zhang, Qian Mironova, Varvara Santos-Neto, Alvaro Hsu, Kuo-Shun Rattray, Zahra Cross, Justin R. Zhang, Yawei Paty, Philip B. Khan, Sajid A. Johnson, Caroline H. Sci Rep Article Women have a lower incidence of colorectal cancer (CRC) than men, however, they have a higher incidence of right-sided colon cancer (RCC). This is of concern as patients with RCC have the poorest clinical outcomes among all CRC patients. Aberrant metabolism is a known hallmark and therapeutic target for cancer. We propose that metabolic subphenotypes exist between CRCs due to intertumoral molecular and genomic variation, and differences in environmental milieu of the colon which vary between the sexes. Metabolomics analysis of patient colon tumors (n = 197) and normal tissues (n = 39) revealed sex-specific metabolic subphenotypes dependent on anatomic location. Tumors from women with RCC were nutrient-deplete, showing enhanced energy production to fuel asparagine synthesis and amino acid uptake. The clinical importance of our findings were further investigated in an independent data set from The Cancer Genomic Atlas, and demonstrated that high asparagine synthetase (ASNS) expression correlated with poorer survival for women. This is the first study to show a unique, nutrient-deplete metabolic subphenotype in women with RCC, with implications for tumor progression and outcomes in CRC patients. Nature Publishing Group UK 2020-03-17 /pmc/articles/PMC7078199/ /pubmed/32184446 http://dx.doi.org/10.1038/s41598-020-61851-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cai, Yuping Rattray, Nicholas J. W. Zhang, Qian Mironova, Varvara Santos-Neto, Alvaro Hsu, Kuo-Shun Rattray, Zahra Cross, Justin R. Zhang, Yawei Paty, Philip B. Khan, Sajid A. Johnson, Caroline H. Sex Differences in Colon Cancer Metabolism Reveal A Novel Subphenotype |
title | Sex Differences in Colon Cancer Metabolism Reveal A Novel Subphenotype |
title_full | Sex Differences in Colon Cancer Metabolism Reveal A Novel Subphenotype |
title_fullStr | Sex Differences in Colon Cancer Metabolism Reveal A Novel Subphenotype |
title_full_unstemmed | Sex Differences in Colon Cancer Metabolism Reveal A Novel Subphenotype |
title_short | Sex Differences in Colon Cancer Metabolism Reveal A Novel Subphenotype |
title_sort | sex differences in colon cancer metabolism reveal a novel subphenotype |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078199/ https://www.ncbi.nlm.nih.gov/pubmed/32184446 http://dx.doi.org/10.1038/s41598-020-61851-0 |
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