Cargando…
Serum metabolomic profile as a means to distinguish stage of colorectal cancer
BACKGROUND: Presently, colorectal cancer (CRC) is staged preoperatively by radiographic tests, and postoperatively by pathological evaluation of available surgical specimens. However, present staging methods do not accurately identify occult metastases. This has a direct effect on clinical managemen...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506908/ https://www.ncbi.nlm.nih.gov/pubmed/22583555 http://dx.doi.org/10.1186/gm341 |
_version_ | 1782250977394425856 |
---|---|
author | Farshidfar, Farshad Weljie, Aalim M Kopciuk, Karen Buie, W Don MacLean, Anthony Dixon, Elijah Sutherland, Francis R Molckovsky, Andrea Vogel, Hans J Bathe, Oliver F |
author_facet | Farshidfar, Farshad Weljie, Aalim M Kopciuk, Karen Buie, W Don MacLean, Anthony Dixon, Elijah Sutherland, Francis R Molckovsky, Andrea Vogel, Hans J Bathe, Oliver F |
author_sort | Farshidfar, Farshad |
collection | PubMed |
description | BACKGROUND: Presently, colorectal cancer (CRC) is staged preoperatively by radiographic tests, and postoperatively by pathological evaluation of available surgical specimens. However, present staging methods do not accurately identify occult metastases. This has a direct effect on clinical management. Early identification of metastases isolated to the liver may enable surgical resection, whereas more disseminated disease may be best treated with palliative chemotherapy. METHODS: Sera from 103 patients with colorectal adenocarcinoma treated at the same tertiary cancer center were analyzed by proton nuclear magnetic resonance ((1)H NMR) spectroscopy and gas chromatography-mass spectroscopy (GC-MS). Metabolic profiling was done using both supervised pattern recognition and orthogonal partial least squares-discriminant analysis (O-PLS-DA) of the most significant metabolites, which enables comparison of the whole sample spectrum between groups. The metabolomic profiles generated from each platform were compared between the following groups: locoregional CRC (N = 42); liver-only metastases (N = 45); and extrahepatic metastases (N = 25). RESULTS: The serum metabolomic profile associated with locoregional CRC was distinct from that associated with liver-only metastases, based on (1)H NMR spectroscopy (P = 5.10 × 10(-7)) and GC-MS (P = 1.79 × 10(-7)). Similarly, the serum metabolomic profile differed significantly between patients with liver-only metastases and with extrahepatic metastases. The change in metabolomic profile was most markedly demonstrated on GC-MS (P = 4.75 × 10(-5)). CONCLUSIONS: In CRC, the serum metabolomic profile changes markedly with metastasis, and site of disease also appears to affect the pattern of circulating metabolites. This novel observation may have clinical utility in enhancing staging accuracy and selecting patients for surgical or medical management. Additional studies are required to determine the sensitivity of this approach to detect subtle or occult metastatic disease. |
format | Online Article Text |
id | pubmed-3506908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35069082012-11-28 Serum metabolomic profile as a means to distinguish stage of colorectal cancer Farshidfar, Farshad Weljie, Aalim M Kopciuk, Karen Buie, W Don MacLean, Anthony Dixon, Elijah Sutherland, Francis R Molckovsky, Andrea Vogel, Hans J Bathe, Oliver F Genome Med Research BACKGROUND: Presently, colorectal cancer (CRC) is staged preoperatively by radiographic tests, and postoperatively by pathological evaluation of available surgical specimens. However, present staging methods do not accurately identify occult metastases. This has a direct effect on clinical management. Early identification of metastases isolated to the liver may enable surgical resection, whereas more disseminated disease may be best treated with palliative chemotherapy. METHODS: Sera from 103 patients with colorectal adenocarcinoma treated at the same tertiary cancer center were analyzed by proton nuclear magnetic resonance ((1)H NMR) spectroscopy and gas chromatography-mass spectroscopy (GC-MS). Metabolic profiling was done using both supervised pattern recognition and orthogonal partial least squares-discriminant analysis (O-PLS-DA) of the most significant metabolites, which enables comparison of the whole sample spectrum between groups. The metabolomic profiles generated from each platform were compared between the following groups: locoregional CRC (N = 42); liver-only metastases (N = 45); and extrahepatic metastases (N = 25). RESULTS: The serum metabolomic profile associated with locoregional CRC was distinct from that associated with liver-only metastases, based on (1)H NMR spectroscopy (P = 5.10 × 10(-7)) and GC-MS (P = 1.79 × 10(-7)). Similarly, the serum metabolomic profile differed significantly between patients with liver-only metastases and with extrahepatic metastases. The change in metabolomic profile was most markedly demonstrated on GC-MS (P = 4.75 × 10(-5)). CONCLUSIONS: In CRC, the serum metabolomic profile changes markedly with metastasis, and site of disease also appears to affect the pattern of circulating metabolites. This novel observation may have clinical utility in enhancing staging accuracy and selecting patients for surgical or medical management. Additional studies are required to determine the sensitivity of this approach to detect subtle or occult metastatic disease. BioMed Central 2012-05-14 /pmc/articles/PMC3506908/ /pubmed/22583555 http://dx.doi.org/10.1186/gm341 Text en Copyright ©2012 Farshidfar et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Farshidfar, Farshad Weljie, Aalim M Kopciuk, Karen Buie, W Don MacLean, Anthony Dixon, Elijah Sutherland, Francis R Molckovsky, Andrea Vogel, Hans J Bathe, Oliver F Serum metabolomic profile as a means to distinguish stage of colorectal cancer |
title | Serum metabolomic profile as a means to distinguish stage of colorectal cancer |
title_full | Serum metabolomic profile as a means to distinguish stage of colorectal cancer |
title_fullStr | Serum metabolomic profile as a means to distinguish stage of colorectal cancer |
title_full_unstemmed | Serum metabolomic profile as a means to distinguish stage of colorectal cancer |
title_short | Serum metabolomic profile as a means to distinguish stage of colorectal cancer |
title_sort | serum metabolomic profile as a means to distinguish stage of colorectal cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506908/ https://www.ncbi.nlm.nih.gov/pubmed/22583555 http://dx.doi.org/10.1186/gm341 |
work_keys_str_mv | AT farshidfarfarshad serummetabolomicprofileasameanstodistinguishstageofcolorectalcancer AT weljieaalimm serummetabolomicprofileasameanstodistinguishstageofcolorectalcancer AT kopciukkaren serummetabolomicprofileasameanstodistinguishstageofcolorectalcancer AT buiewdon serummetabolomicprofileasameanstodistinguishstageofcolorectalcancer AT macleananthony serummetabolomicprofileasameanstodistinguishstageofcolorectalcancer AT dixonelijah serummetabolomicprofileasameanstodistinguishstageofcolorectalcancer AT sutherlandfrancisr serummetabolomicprofileasameanstodistinguishstageofcolorectalcancer AT molckovskyandrea serummetabolomicprofileasameanstodistinguishstageofcolorectalcancer AT vogelhansj serummetabolomicprofileasameanstodistinguishstageofcolorectalcancer AT batheoliverf serummetabolomicprofileasameanstodistinguishstageofcolorectalcancer |