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Metabolome analysis reveals a diversity of cancer tissues in advanced epithelial ovarian cancer

BACKGROUND: Epithelial ovarian cancer remains one of the leading causes of cancer deaths among women worldwide, and advanced epithelial ovarian cancer frequently metastasizes to the omentum. The characteristics of metastatic cancer may differ from those of primary ovarian cancer and reflect the uniq...

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Autores principales: Yoshida, Kosuke, Yoshikawa, Nobuhisa, Kitami, Kazuhisa, Tamauchi, Satoshi, Ikeda, Yoshiki, Yokoi, Akira, Nishino, Kimihiro, Niimi, Kaoru, Kajiyama, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207638/
https://www.ncbi.nlm.nih.gov/pubmed/34134729
http://dx.doi.org/10.1186/s12935-021-02014-7
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author Yoshida, Kosuke
Yoshikawa, Nobuhisa
Kitami, Kazuhisa
Tamauchi, Satoshi
Ikeda, Yoshiki
Yokoi, Akira
Nishino, Kimihiro
Niimi, Kaoru
Kajiyama, Hiroaki
author_facet Yoshida, Kosuke
Yoshikawa, Nobuhisa
Kitami, Kazuhisa
Tamauchi, Satoshi
Ikeda, Yoshiki
Yokoi, Akira
Nishino, Kimihiro
Niimi, Kaoru
Kajiyama, Hiroaki
author_sort Yoshida, Kosuke
collection PubMed
description BACKGROUND: Epithelial ovarian cancer remains one of the leading causes of cancer deaths among women worldwide, and advanced epithelial ovarian cancer frequently metastasizes to the omentum. The characteristics of metastatic cancer may differ from those of primary ovarian cancer and reflect the unique omental microenvironment. This study investigated metabolomic differences in epithelial ovarian cancers. METHODS: Patients with advanced epithelial ovarian cancer were eligible for this study. Five patients underwent surgery and resection of paired primary ovarian and omental metastatic cancer at Nagoya University. Metabolome analysis was performed in these paired cancer and metastatic cancer tissues through a facility service (C-SCOPE) at Human Metabolome Technologies, Inc. The concentrations of 116 compounds were measured by CE-TOFMS and CE-QqQMS, and 30 metabolic parameters were calculated. For statistical analyses, Welch’s t-test was used for comparisons between two independent groups. RESULTS: Metabolite profiles were all different, which reflects diversity among these cancer tissues. Of the measured compounds, urea was the only metabolite that was significantly decreased in omental metastatic cancers compared with the primary cancers (p = 0.031). Moreover, in omental metastatic cancers, the pentose phosphate pathway was more dominant than glycolysis. Furthermore, in some cases, lactic acids in omental metastatic cancers were markedly decreased compared with primary cancers. With regard to histological subtype, the total levels of amino acids, especially the percentage of glutamine, were significantly enriched in serous carcinomas compared with nonserous carcinomas (p = 0.004 and p = 0.001). Moreover, the reduced forms of glutathione and polyamines were also more abundant in serous carcinomas than in nonserous carcinomas (p = 0.025 and 0.048). CONCLUSIONS: The metabolite profiles differed depending on tumor location and histological subtype. Metabolome analysis may be a useful tool for identifying cancer diagnostic and prognostic markers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-02014-7.
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spelling pubmed-82076382021-06-16 Metabolome analysis reveals a diversity of cancer tissues in advanced epithelial ovarian cancer Yoshida, Kosuke Yoshikawa, Nobuhisa Kitami, Kazuhisa Tamauchi, Satoshi Ikeda, Yoshiki Yokoi, Akira Nishino, Kimihiro Niimi, Kaoru Kajiyama, Hiroaki Cancer Cell Int Primary Research BACKGROUND: Epithelial ovarian cancer remains one of the leading causes of cancer deaths among women worldwide, and advanced epithelial ovarian cancer frequently metastasizes to the omentum. The characteristics of metastatic cancer may differ from those of primary ovarian cancer and reflect the unique omental microenvironment. This study investigated metabolomic differences in epithelial ovarian cancers. METHODS: Patients with advanced epithelial ovarian cancer were eligible for this study. Five patients underwent surgery and resection of paired primary ovarian and omental metastatic cancer at Nagoya University. Metabolome analysis was performed in these paired cancer and metastatic cancer tissues through a facility service (C-SCOPE) at Human Metabolome Technologies, Inc. The concentrations of 116 compounds were measured by CE-TOFMS and CE-QqQMS, and 30 metabolic parameters were calculated. For statistical analyses, Welch’s t-test was used for comparisons between two independent groups. RESULTS: Metabolite profiles were all different, which reflects diversity among these cancer tissues. Of the measured compounds, urea was the only metabolite that was significantly decreased in omental metastatic cancers compared with the primary cancers (p = 0.031). Moreover, in omental metastatic cancers, the pentose phosphate pathway was more dominant than glycolysis. Furthermore, in some cases, lactic acids in omental metastatic cancers were markedly decreased compared with primary cancers. With regard to histological subtype, the total levels of amino acids, especially the percentage of glutamine, were significantly enriched in serous carcinomas compared with nonserous carcinomas (p = 0.004 and p = 0.001). Moreover, the reduced forms of glutathione and polyamines were also more abundant in serous carcinomas than in nonserous carcinomas (p = 0.025 and 0.048). CONCLUSIONS: The metabolite profiles differed depending on tumor location and histological subtype. Metabolome analysis may be a useful tool for identifying cancer diagnostic and prognostic markers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-02014-7. BioMed Central 2021-06-16 /pmc/articles/PMC8207638/ /pubmed/34134729 http://dx.doi.org/10.1186/s12935-021-02014-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Primary Research
Yoshida, Kosuke
Yoshikawa, Nobuhisa
Kitami, Kazuhisa
Tamauchi, Satoshi
Ikeda, Yoshiki
Yokoi, Akira
Nishino, Kimihiro
Niimi, Kaoru
Kajiyama, Hiroaki
Metabolome analysis reveals a diversity of cancer tissues in advanced epithelial ovarian cancer
title Metabolome analysis reveals a diversity of cancer tissues in advanced epithelial ovarian cancer
title_full Metabolome analysis reveals a diversity of cancer tissues in advanced epithelial ovarian cancer
title_fullStr Metabolome analysis reveals a diversity of cancer tissues in advanced epithelial ovarian cancer
title_full_unstemmed Metabolome analysis reveals a diversity of cancer tissues in advanced epithelial ovarian cancer
title_short Metabolome analysis reveals a diversity of cancer tissues in advanced epithelial ovarian cancer
title_sort metabolome analysis reveals a diversity of cancer tissues in advanced epithelial ovarian cancer
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207638/
https://www.ncbi.nlm.nih.gov/pubmed/34134729
http://dx.doi.org/10.1186/s12935-021-02014-7
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