Secretome Identifies Tenascin-X as a Potent Marker of Ovarian Cancer
CA-125 has been a valuable marker for the follow-up of ovarian cancer patients but it is not sensitive enough to be used as diagnostic marker. We had already used secretomic methods to identify proteins differentially secreted by serous ovarian cancer cells compared to healthy ovarian cells. Here, w...
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doaj-11d928c8a2734e43b7574740ca7c61f22020-11-24T21:06:07ZengHindawi LimitedBioMed Research International2314-61332314-61412015-01-01201510.1155/2015/208017208017Secretome Identifies Tenascin-X as a Potent Marker of Ovarian CancerMarianne Kramer0Sandra Pierredon1Pascale Ribaux2Jean-Christophe Tille3Patrick Petignat4Marie Cohen5Department of Gynaecology Obstetrics, Faculty of Medicine, 1211 Geneva 14, SwitzerlandDepartment of Gynaecology Obstetrics, Faculty of Medicine, 1211 Geneva 14, SwitzerlandDepartment of Gynaecology Obstetrics, Faculty of Medicine, 1211 Geneva 14, SwitzerlandDivision of Clinical Pathology, HUG, 1211 Geneva 14, SwitzerlandDepartment of Gynaecology Obstetrics, Faculty of Medicine, 1211 Geneva 14, SwitzerlandDepartment of Gynaecology Obstetrics, Faculty of Medicine, 1211 Geneva 14, SwitzerlandCA-125 has been a valuable marker for the follow-up of ovarian cancer patients but it is not sensitive enough to be used as diagnostic marker. We had already used secretomic methods to identify proteins differentially secreted by serous ovarian cancer cells compared to healthy ovarian cells. Here, we evaluated the secretion of these proteins by ovarian cancer cells during the follow-up of one patient. Proteins that correlated with CA-125 levels were screened using serum samples from ovarian cancer patients as well as benign and healthy controls. Tenascin-X secretion was shown to correlate with CA-125 value in the initial case study. The immunohistochemical detection of increased amount of tenascin-X in ovarian cancer tissues compared to healthy tissues confirms the potent interest in tenascin-X as marker. We then quantified the tenascin-X level in serum of patients and identified tenascin-X as potent marker for ovarian cancer, showing that secretomic analysis is suitable for the identification of protein biomarkers when combined with protein immunoassay. Using this method, we determined tenascin-X as a new potent marker for serous ovarian cancer.http://dx.doi.org/10.1155/2015/208017 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marianne Kramer Sandra Pierredon Pascale Ribaux Jean-Christophe Tille Patrick Petignat Marie Cohen |
spellingShingle |
Marianne Kramer Sandra Pierredon Pascale Ribaux Jean-Christophe Tille Patrick Petignat Marie Cohen Secretome Identifies Tenascin-X as a Potent Marker of Ovarian Cancer BioMed Research International |
author_facet |
Marianne Kramer Sandra Pierredon Pascale Ribaux Jean-Christophe Tille Patrick Petignat Marie Cohen |
author_sort |
Marianne Kramer |
title |
Secretome Identifies Tenascin-X as a Potent Marker of Ovarian Cancer |
title_short |
Secretome Identifies Tenascin-X as a Potent Marker of Ovarian Cancer |
title_full |
Secretome Identifies Tenascin-X as a Potent Marker of Ovarian Cancer |
title_fullStr |
Secretome Identifies Tenascin-X as a Potent Marker of Ovarian Cancer |
title_full_unstemmed |
Secretome Identifies Tenascin-X as a Potent Marker of Ovarian Cancer |
title_sort |
secretome identifies tenascin-x as a potent marker of ovarian cancer |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2015-01-01 |
description |
CA-125 has been a valuable marker for the follow-up of ovarian cancer patients but it is not sensitive enough to be used as diagnostic marker. We had already used secretomic methods to identify proteins differentially secreted by serous ovarian cancer cells compared to healthy ovarian cells. Here, we evaluated the secretion of these proteins by ovarian cancer cells during the follow-up of one patient. Proteins that correlated with CA-125 levels were screened using serum samples from ovarian cancer patients as well as benign and healthy controls. Tenascin-X secretion was shown to correlate with CA-125 value in the initial case study. The immunohistochemical detection of increased amount of tenascin-X in ovarian cancer tissues compared to healthy tissues confirms the potent interest in tenascin-X as marker. We then quantified the tenascin-X level in serum of patients and identified tenascin-X as potent marker for ovarian cancer, showing that secretomic analysis is suitable for the identification of protein biomarkers when combined with protein immunoassay. Using this method, we determined tenascin-X as a new potent marker for serous ovarian cancer. |
url |
http://dx.doi.org/10.1155/2015/208017 |
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