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Interleukin-6 and leptin as markers of energy metabolicchanges in advanced ovarian cancer patients

The progression of the neoplastic disease is characterized by specific alterations of energy metabolism and by symptoms like fatigue, anorexia, nausea, anaemia, immunodepression and poor performance status (PS). The main cause of these symptoms and metabolic abnormalities is the chronic action of pr...

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Autores principales: Macciò, Antonio, Madeddu, Clelia, Massa, Daniela, Astara, Giorgio, Farci, Daniele, Melis, Gian Benedetto, Mantovani, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4516542/
https://www.ncbi.nlm.nih.gov/pubmed/18624749
http://dx.doi.org/10.1111/j.1582-4934.2008.00408.x
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author Macciò, Antonio
Madeddu, Clelia
Massa, Daniela
Astara, Giorgio
Farci, Daniele
Melis, Gian Benedetto
Mantovani, Giovanni
author_facet Macciò, Antonio
Madeddu, Clelia
Massa, Daniela
Astara, Giorgio
Farci, Daniele
Melis, Gian Benedetto
Mantovani, Giovanni
author_sort Macciò, Antonio
collection PubMed
description The progression of the neoplastic disease is characterized by specific alterations of energy metabolism and by symptoms like fatigue, anorexia, nausea, anaemia, immunodepression and poor performance status (PS). The main cause of these symptoms and metabolic abnormalities is the chronic action of proinflammatory cytokines released both by tumour and immune cells. The present study aimed to assess the relationship between markers of inflammation (C-Reactive Protein, Fibrinogen, proinflammatory cytokines) and energy metabolic status (BMI, leptin, oxidative stress) according to clinical parameters in 104 ovarian cancer patients at different stage and, moreover, to evaluate prospectively the changes of these parameters in accordance to tumour response in a subgroup of 70 advanced stage ovarian cancer patients. Advanced stage and poor PS were associated to high-grade inflammation and impaired energy metabolism. Among inflammatory mediators, interleukin (IL)-6 had a central role as predictive factor of leptin, reactive oxygen species and glutathione peroxidase. In turn, leptin considered the key marker of the nutritional status and energy metabolism, was independently determined from stage and IL-6, not only from BMI. Moreover, the evaluation of the changes of these parameters during the course of the neoplastic disease in the subgroup of advanced ovarian cancer patients clearly unveils the central role of IL-6 and leptin as early markers of the metabolic alterations and symptoms associated to disease progression in advanced stage ovarian cancer. Their assessment should be included in monitoring disease outcome, especially when cancer is no longer curable and quality of life becomes the primary endpoint.
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spelling pubmed-45165422015-08-03 Interleukin-6 and leptin as markers of energy metabolicchanges in advanced ovarian cancer patients Macciò, Antonio Madeddu, Clelia Massa, Daniela Astara, Giorgio Farci, Daniele Melis, Gian Benedetto Mantovani, Giovanni J Cell Mol Med Molecular Oncology The progression of the neoplastic disease is characterized by specific alterations of energy metabolism and by symptoms like fatigue, anorexia, nausea, anaemia, immunodepression and poor performance status (PS). The main cause of these symptoms and metabolic abnormalities is the chronic action of proinflammatory cytokines released both by tumour and immune cells. The present study aimed to assess the relationship between markers of inflammation (C-Reactive Protein, Fibrinogen, proinflammatory cytokines) and energy metabolic status (BMI, leptin, oxidative stress) according to clinical parameters in 104 ovarian cancer patients at different stage and, moreover, to evaluate prospectively the changes of these parameters in accordance to tumour response in a subgroup of 70 advanced stage ovarian cancer patients. Advanced stage and poor PS were associated to high-grade inflammation and impaired energy metabolism. Among inflammatory mediators, interleukin (IL)-6 had a central role as predictive factor of leptin, reactive oxygen species and glutathione peroxidase. In turn, leptin considered the key marker of the nutritional status and energy metabolism, was independently determined from stage and IL-6, not only from BMI. Moreover, the evaluation of the changes of these parameters during the course of the neoplastic disease in the subgroup of advanced ovarian cancer patients clearly unveils the central role of IL-6 and leptin as early markers of the metabolic alterations and symptoms associated to disease progression in advanced stage ovarian cancer. Their assessment should be included in monitoring disease outcome, especially when cancer is no longer curable and quality of life becomes the primary endpoint. John Wiley & Sons, Ltd 2009-09 2008-07-08 /pmc/articles/PMC4516542/ /pubmed/18624749 http://dx.doi.org/10.1111/j.1582-4934.2008.00408.x Text en © 2008 The Authors Journal compilation © 2009 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Molecular Oncology
Macciò, Antonio
Madeddu, Clelia
Massa, Daniela
Astara, Giorgio
Farci, Daniele
Melis, Gian Benedetto
Mantovani, Giovanni
Interleukin-6 and leptin as markers of energy metabolicchanges in advanced ovarian cancer patients
title Interleukin-6 and leptin as markers of energy metabolicchanges in advanced ovarian cancer patients
title_full Interleukin-6 and leptin as markers of energy metabolicchanges in advanced ovarian cancer patients
title_fullStr Interleukin-6 and leptin as markers of energy metabolicchanges in advanced ovarian cancer patients
title_full_unstemmed Interleukin-6 and leptin as markers of energy metabolicchanges in advanced ovarian cancer patients
title_short Interleukin-6 and leptin as markers of energy metabolicchanges in advanced ovarian cancer patients
title_sort interleukin-6 and leptin as markers of energy metabolicchanges in advanced ovarian cancer patients
topic Molecular Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4516542/
https://www.ncbi.nlm.nih.gov/pubmed/18624749
http://dx.doi.org/10.1111/j.1582-4934.2008.00408.x
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