Cargando…

Multi-Omic Profiling of Multi-Biosamples Reveals the Role of Amino Acid and Nucleotide Metabolism in Endometrial Cancer

BACKGROUND: Endometrial cancer (EC) is one of the most common gynecological cancers. The traditional diagnosis of EC relies on histopathology, which, however, is invasive and may arouse tumor spread. There have been many studies aiming to find the metabolomic biomarkers of EC to improve the early di...

Descripción completa

Detalles Bibliográficos
Autores principales: Yi, Runqiu, Xie, Liying, Wang, Xiaoqing, Shen, Chengpin, Chen, Xiaojun, Qiao, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099206/
https://www.ncbi.nlm.nih.gov/pubmed/35574395
http://dx.doi.org/10.3389/fonc.2022.861142
_version_ 1784706552779767808
author Yi, Runqiu
Xie, Liying
Wang, Xiaoqing
Shen, Chengpin
Chen, Xiaojun
Qiao, Liang
author_facet Yi, Runqiu
Xie, Liying
Wang, Xiaoqing
Shen, Chengpin
Chen, Xiaojun
Qiao, Liang
author_sort Yi, Runqiu
collection PubMed
description BACKGROUND: Endometrial cancer (EC) is one of the most common gynecological cancers. The traditional diagnosis of EC relies on histopathology, which, however, is invasive and may arouse tumor spread. There have been many studies aiming to find the metabolomic biomarkers of EC to improve the early diagnosis of cancer in a non-invasive or minimally invasive way, which can also provide valuable information for understanding the disease. However, most of these studies only analyze a single type of sample by metabolomics, and cannot provide a comprehensive view of the altered metabolism in EC patients. Our study tries to gain a pathway-based view of multiple types of samples for understanding metabolomic disorders in EC by combining metabolomics and proteomics. METHODS: Forty-four EC patients and forty-three controls were recruited for the research. We collected endometrial tissue, urine, and intrauterine brushing samples. Untargeted metabolomics and untargeted proteomics were both performed on the endometrial tissue samples, while only untargeted metabolomics was performed on the urine and intrauterine brushing samples. RESULTS: By integrating the differential metabolites and proteins between EC patients and controls detected in the endometrial tissue samples, we identified several EC-related significant pathways, such as amino acid metabolism and nucleotide metabolism. The significance of these pathways and the potential of metabolite biomarker-based diagnosis were then further verified by using urine and intrauterine brushing samples. It was found that the regulation of metabolites involved in the significant pathways showed similar trends in the intrauterine brushings and the endometrial tissue samples, while opposite trends in the urine and the endometrial tissue samples. CONCLUSIONS: With multi-omics characterization of multi-biosamples, the metabolomic changes related to EC are illustrated in a pathway-based way. The network of altered metabolites and related proteins provides a comprehensive view of altered metabolism in the endometrial tissue samples. The verification of these critical pathways by using urine and intrauterine brushing samples provides evidence for the possible non-invasive or minimally invasive biopsy for EC diagnosis in the future.
format Online
Article
Text
id pubmed-9099206
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-90992062022-05-14 Multi-Omic Profiling of Multi-Biosamples Reveals the Role of Amino Acid and Nucleotide Metabolism in Endometrial Cancer Yi, Runqiu Xie, Liying Wang, Xiaoqing Shen, Chengpin Chen, Xiaojun Qiao, Liang Front Oncol Oncology BACKGROUND: Endometrial cancer (EC) is one of the most common gynecological cancers. The traditional diagnosis of EC relies on histopathology, which, however, is invasive and may arouse tumor spread. There have been many studies aiming to find the metabolomic biomarkers of EC to improve the early diagnosis of cancer in a non-invasive or minimally invasive way, which can also provide valuable information for understanding the disease. However, most of these studies only analyze a single type of sample by metabolomics, and cannot provide a comprehensive view of the altered metabolism in EC patients. Our study tries to gain a pathway-based view of multiple types of samples for understanding metabolomic disorders in EC by combining metabolomics and proteomics. METHODS: Forty-four EC patients and forty-three controls were recruited for the research. We collected endometrial tissue, urine, and intrauterine brushing samples. Untargeted metabolomics and untargeted proteomics were both performed on the endometrial tissue samples, while only untargeted metabolomics was performed on the urine and intrauterine brushing samples. RESULTS: By integrating the differential metabolites and proteins between EC patients and controls detected in the endometrial tissue samples, we identified several EC-related significant pathways, such as amino acid metabolism and nucleotide metabolism. The significance of these pathways and the potential of metabolite biomarker-based diagnosis were then further verified by using urine and intrauterine brushing samples. It was found that the regulation of metabolites involved in the significant pathways showed similar trends in the intrauterine brushings and the endometrial tissue samples, while opposite trends in the urine and the endometrial tissue samples. CONCLUSIONS: With multi-omics characterization of multi-biosamples, the metabolomic changes related to EC are illustrated in a pathway-based way. The network of altered metabolites and related proteins provides a comprehensive view of altered metabolism in the endometrial tissue samples. The verification of these critical pathways by using urine and intrauterine brushing samples provides evidence for the possible non-invasive or minimally invasive biopsy for EC diagnosis in the future. Frontiers Media S.A. 2022-04-29 /pmc/articles/PMC9099206/ /pubmed/35574395 http://dx.doi.org/10.3389/fonc.2022.861142 Text en Copyright © 2022 Yi, Xie, Wang, Shen, Chen and Qiao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Yi, Runqiu
Xie, Liying
Wang, Xiaoqing
Shen, Chengpin
Chen, Xiaojun
Qiao, Liang
Multi-Omic Profiling of Multi-Biosamples Reveals the Role of Amino Acid and Nucleotide Metabolism in Endometrial Cancer
title Multi-Omic Profiling of Multi-Biosamples Reveals the Role of Amino Acid and Nucleotide Metabolism in Endometrial Cancer
title_full Multi-Omic Profiling of Multi-Biosamples Reveals the Role of Amino Acid and Nucleotide Metabolism in Endometrial Cancer
title_fullStr Multi-Omic Profiling of Multi-Biosamples Reveals the Role of Amino Acid and Nucleotide Metabolism in Endometrial Cancer
title_full_unstemmed Multi-Omic Profiling of Multi-Biosamples Reveals the Role of Amino Acid and Nucleotide Metabolism in Endometrial Cancer
title_short Multi-Omic Profiling of Multi-Biosamples Reveals the Role of Amino Acid and Nucleotide Metabolism in Endometrial Cancer
title_sort multi-omic profiling of multi-biosamples reveals the role of amino acid and nucleotide metabolism in endometrial cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099206/
https://www.ncbi.nlm.nih.gov/pubmed/35574395
http://dx.doi.org/10.3389/fonc.2022.861142
work_keys_str_mv AT yirunqiu multiomicprofilingofmultibiosamplesrevealstheroleofaminoacidandnucleotidemetabolisminendometrialcancer
AT xieliying multiomicprofilingofmultibiosamplesrevealstheroleofaminoacidandnucleotidemetabolisminendometrialcancer
AT wangxiaoqing multiomicprofilingofmultibiosamplesrevealstheroleofaminoacidandnucleotidemetabolisminendometrialcancer
AT shenchengpin multiomicprofilingofmultibiosamplesrevealstheroleofaminoacidandnucleotidemetabolisminendometrialcancer
AT chenxiaojun multiomicprofilingofmultibiosamplesrevealstheroleofaminoacidandnucleotidemetabolisminendometrialcancer
AT qiaoliang multiomicprofilingofmultibiosamplesrevealstheroleofaminoacidandnucleotidemetabolisminendometrialcancer