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Clinical Significance of Plasma Levels of Gluconeogenic Amino Acids in Esophageal Cancer Patients

OBJECTIVE: Metabolic processes in the body of people with and without esophageal cancer (EC) are significantly different. Therefore, changes in the metabolism of amino acids in the body of EC patients can lead to metabolic disorders, such as increased gluconeogenesis. The aim of this study was the c...

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Autores principales: Taherizadeh, Mahsa, Khoshnia, Masoud, Shams, Sedigheh, Hesari, Zahra, Joshaghani, Hamidreza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771918/
https://www.ncbi.nlm.nih.gov/pubmed/32856879
http://dx.doi.org/10.31557/APJCP.2020.21.8.2463
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author Taherizadeh, Mahsa
Khoshnia, Masoud
Shams, Sedigheh
Hesari, Zahra
Joshaghani, Hamidreza
author_facet Taherizadeh, Mahsa
Khoshnia, Masoud
Shams, Sedigheh
Hesari, Zahra
Joshaghani, Hamidreza
author_sort Taherizadeh, Mahsa
collection PubMed
description OBJECTIVE: Metabolic processes in the body of people with and without esophageal cancer (EC) are significantly different. Therefore, changes in the metabolism of amino acids in the body of EC patients can lead to metabolic disorders, such as increased gluconeogenesis. The aim of this study was the comparison of the plasma levels of gluconeogenic amino acids between patients with EC and the control group. METHODS: Plasma samples of 37 patients with EC who were selected before any treatment or surgery, and 37 healthy adults who did not have history of family cancer and malignant diseases were taken. Analysis of the plasma levels of amino acids including, alanine, asparagine, aspartate, glutamate, glutamine, glycine, serine, arginine, histidine, methionine, threonine, valine, tyrosine, isoleucine, phenylalanine, tryptophan was done by High Performance Liquid Chromatography (HPLC) based on reverse-phase-chromatography. Data analysis was done by SPSS-16 software. RESULTS: In the patient group the mean age ± SD was 63±13.64 and 21 (56.8%) were male.The plasma levels of the alanine, asparagine, histidine, methionine, threonine, valine amino acids in the patients with esophageal cancer was significantly reduced and glycine was increased (p-value<0.05). CONCLUSION: Gluconeogenic amino acids are the main precursor of glucose synthesis in the gluconeogenesis pathway. Cancer cells need more energy to grow and multiply, and glucose is used as the main fuel for cells. Given the importance of metabolic pathways in cancer cells, more detailed studies at the molecular level can provide new insights into early detection and appropriate treatment strategies for cancer.
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spelling pubmed-77719182021-02-06 Clinical Significance of Plasma Levels of Gluconeogenic Amino Acids in Esophageal Cancer Patients Taherizadeh, Mahsa Khoshnia, Masoud Shams, Sedigheh Hesari, Zahra Joshaghani, Hamidreza Asian Pac J Cancer Prev Research Article OBJECTIVE: Metabolic processes in the body of people with and without esophageal cancer (EC) are significantly different. Therefore, changes in the metabolism of amino acids in the body of EC patients can lead to metabolic disorders, such as increased gluconeogenesis. The aim of this study was the comparison of the plasma levels of gluconeogenic amino acids between patients with EC and the control group. METHODS: Plasma samples of 37 patients with EC who were selected before any treatment or surgery, and 37 healthy adults who did not have history of family cancer and malignant diseases were taken. Analysis of the plasma levels of amino acids including, alanine, asparagine, aspartate, glutamate, glutamine, glycine, serine, arginine, histidine, methionine, threonine, valine, tyrosine, isoleucine, phenylalanine, tryptophan was done by High Performance Liquid Chromatography (HPLC) based on reverse-phase-chromatography. Data analysis was done by SPSS-16 software. RESULTS: In the patient group the mean age ± SD was 63±13.64 and 21 (56.8%) were male.The plasma levels of the alanine, asparagine, histidine, methionine, threonine, valine amino acids in the patients with esophageal cancer was significantly reduced and glycine was increased (p-value<0.05). CONCLUSION: Gluconeogenic amino acids are the main precursor of glucose synthesis in the gluconeogenesis pathway. Cancer cells need more energy to grow and multiply, and glucose is used as the main fuel for cells. Given the importance of metabolic pathways in cancer cells, more detailed studies at the molecular level can provide new insights into early detection and appropriate treatment strategies for cancer. West Asia Organization for Cancer Prevention 2020-08 /pmc/articles/PMC7771918/ /pubmed/32856879 http://dx.doi.org/10.31557/APJCP.2020.21.8.2463 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Taherizadeh, Mahsa
Khoshnia, Masoud
Shams, Sedigheh
Hesari, Zahra
Joshaghani, Hamidreza
Clinical Significance of Plasma Levels of Gluconeogenic Amino Acids in Esophageal Cancer Patients
title Clinical Significance of Plasma Levels of Gluconeogenic Amino Acids in Esophageal Cancer Patients
title_full Clinical Significance of Plasma Levels of Gluconeogenic Amino Acids in Esophageal Cancer Patients
title_fullStr Clinical Significance of Plasma Levels of Gluconeogenic Amino Acids in Esophageal Cancer Patients
title_full_unstemmed Clinical Significance of Plasma Levels of Gluconeogenic Amino Acids in Esophageal Cancer Patients
title_short Clinical Significance of Plasma Levels of Gluconeogenic Amino Acids in Esophageal Cancer Patients
title_sort clinical significance of plasma levels of gluconeogenic amino acids in esophageal cancer patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771918/
https://www.ncbi.nlm.nih.gov/pubmed/32856879
http://dx.doi.org/10.31557/APJCP.2020.21.8.2463
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