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The Distinctive Serum Metabolomes of Gastric, Esophageal and Colorectal Cancers
SIMPLE SUMMARY: Cancer of the stomach, esophagus and colon are often fatal. Ways are being sought to establish patient-friendly screening tests that would allow these cancers to be detected earlier. Examination of the metabolomics results of cancer patient’s serum for certain metabolites unique for...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916516/ https://www.ncbi.nlm.nih.gov/pubmed/33578739 http://dx.doi.org/10.3390/cancers13040720 |
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author | Ren, Zhenxing Rajani, Cynthia Jia, Wei |
author_facet | Ren, Zhenxing Rajani, Cynthia Jia, Wei |
author_sort | Ren, Zhenxing |
collection | PubMed |
description | SIMPLE SUMMARY: Cancer of the stomach, esophagus and colon are often fatal. Ways are being sought to establish patient-friendly screening tests that would allow these cancers to be detected earlier. Examination of the metabolomics results of cancer patient’s serum for certain metabolites unique for a particular cancer was the goal of this review. From studies conducted within the past five years several metabolites were found to be changed in cancer compared to non-cancer patients for each of the three cancers. Further confirmation of what was discovered in this review coupled with establishment of standard protocols may allow for cancer screening on patient blood samples to become routine clinical tests. ABSTRACT: Three of the most lethal cancers in the world are the gastrointestinal cancers—gastric (GC), esophageal (EC) and colorectal cancer (CRC)—which are ranked as third, sixth and fourth in cancer deaths globally. Early detection of these cancers is difficult, and a quest is currently on to find non-invasive screening tests to detect these cancers. The reprogramming of energy metabolism is a hallmark of cancer, notably, an increased dependence on aerobic glycolysis which is often referred to as the Warburg effect. This metabolic change results in a unique metabolic profile that distinguishes cancer cells from normal cells. Serum metabolomics analyses allow one to measure the end products of both host and microbiota metabolism present at the time of sample collection. It is a non-invasive procedure requiring only blood collection which encourages greater patient compliance to have more frequent screenings for cancer. In the following review we will examine some of the most current serum metabolomics studies in order to compare their results and test a hypothesis that different tumors, notably, from EC, GC and CRC, have distinguishing serum metabolite profiles. |
format | Online Article Text |
id | pubmed-7916516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79165162021-03-01 The Distinctive Serum Metabolomes of Gastric, Esophageal and Colorectal Cancers Ren, Zhenxing Rajani, Cynthia Jia, Wei Cancers (Basel) Review SIMPLE SUMMARY: Cancer of the stomach, esophagus and colon are often fatal. Ways are being sought to establish patient-friendly screening tests that would allow these cancers to be detected earlier. Examination of the metabolomics results of cancer patient’s serum for certain metabolites unique for a particular cancer was the goal of this review. From studies conducted within the past five years several metabolites were found to be changed in cancer compared to non-cancer patients for each of the three cancers. Further confirmation of what was discovered in this review coupled with establishment of standard protocols may allow for cancer screening on patient blood samples to become routine clinical tests. ABSTRACT: Three of the most lethal cancers in the world are the gastrointestinal cancers—gastric (GC), esophageal (EC) and colorectal cancer (CRC)—which are ranked as third, sixth and fourth in cancer deaths globally. Early detection of these cancers is difficult, and a quest is currently on to find non-invasive screening tests to detect these cancers. The reprogramming of energy metabolism is a hallmark of cancer, notably, an increased dependence on aerobic glycolysis which is often referred to as the Warburg effect. This metabolic change results in a unique metabolic profile that distinguishes cancer cells from normal cells. Serum metabolomics analyses allow one to measure the end products of both host and microbiota metabolism present at the time of sample collection. It is a non-invasive procedure requiring only blood collection which encourages greater patient compliance to have more frequent screenings for cancer. In the following review we will examine some of the most current serum metabolomics studies in order to compare their results and test a hypothesis that different tumors, notably, from EC, GC and CRC, have distinguishing serum metabolite profiles. MDPI 2021-02-10 /pmc/articles/PMC7916516/ /pubmed/33578739 http://dx.doi.org/10.3390/cancers13040720 Text en © 2021 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 | Review Ren, Zhenxing Rajani, Cynthia Jia, Wei The Distinctive Serum Metabolomes of Gastric, Esophageal and Colorectal Cancers |
title | The Distinctive Serum Metabolomes of Gastric, Esophageal and Colorectal Cancers |
title_full | The Distinctive Serum Metabolomes of Gastric, Esophageal and Colorectal Cancers |
title_fullStr | The Distinctive Serum Metabolomes of Gastric, Esophageal and Colorectal Cancers |
title_full_unstemmed | The Distinctive Serum Metabolomes of Gastric, Esophageal and Colorectal Cancers |
title_short | The Distinctive Serum Metabolomes of Gastric, Esophageal and Colorectal Cancers |
title_sort | distinctive serum metabolomes of gastric, esophageal and colorectal cancers |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916516/ https://www.ncbi.nlm.nih.gov/pubmed/33578739 http://dx.doi.org/10.3390/cancers13040720 |
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