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Prognostic significance of specific anti-WT1 IgG antibody level in plasma in patients with ovarian carcinoma
Ovarian carcinoma (OC) has a poor prognosis and lack early effective screening markers. Wilm's tumor gene 1 (WT1) is overexpressed in OCs. Therefore, it is of great interest to investigate whether WT1-specific antibody (Ab) measurements in plasma can serve as a biomarker of anti-OC response, an...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303158/ https://www.ncbi.nlm.nih.gov/pubmed/24715586 http://dx.doi.org/10.1002/cam4.244 |
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author | Andersson, Charlotta Oji, Yusuke Ohlson, Nina Wang, Sihan Li, Xingru Ottander, Ulrika Lundin, Eva Sugiyama, Haruo Li, Aihong |
author_facet | Andersson, Charlotta Oji, Yusuke Ohlson, Nina Wang, Sihan Li, Xingru Ottander, Ulrika Lundin, Eva Sugiyama, Haruo Li, Aihong |
author_sort | Andersson, Charlotta |
collection | PubMed |
description | Ovarian carcinoma (OC) has a poor prognosis and lack early effective screening markers. Wilm's tumor gene 1 (WT1) is overexpressed in OCs. Therefore, it is of great interest to investigate whether WT1-specific antibody (Ab) measurements in plasma can serve as a biomarker of anti-OC response, and is of importance in relation to patient prognosis. Peripheral blood samples were obtained from a total of 103 women with ovarian tumors with median being 1 day (range 0–48 days) before operation. WT1 IgG Ab levels were evaluated using enzyme-linked immunosorbent assay (ELISA). Immunohistochemical analysis of WT1 protein expression was performed on OC tissue samples. We found that low-WT1 Ab level in plasma was related to improved survival in patients diagnosed at stages III–IV and grade 3 carcinomas. Positive WT1 protein staining on OC tissue samples had a negative impact on survival in the entire cohort, both overall survival (OS) (P = 0.046) and progression-free survival (PFS) (P = 0.006), but not in the serous OC subtype. Combining WT1 IgG Ab levels and WT1 staining, patients with high-WT1 IgG Ab levels in plasma and positive WT1 protein staining in cancer tissues had shorter survival, with a significant association in PFS (P = 0.016). These results indicated that WT1 Ab measurements in plasma and WT1 staining in tissue specimens could be useful as biomarkers for patient outcome in the high-risk subtypes of OCs for postoperative individualized therapy. |
format | Online Article Text |
id | pubmed-4303158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43031582015-01-22 Prognostic significance of specific anti-WT1 IgG antibody level in plasma in patients with ovarian carcinoma Andersson, Charlotta Oji, Yusuke Ohlson, Nina Wang, Sihan Li, Xingru Ottander, Ulrika Lundin, Eva Sugiyama, Haruo Li, Aihong Cancer Med Clinical Cancer Research Ovarian carcinoma (OC) has a poor prognosis and lack early effective screening markers. Wilm's tumor gene 1 (WT1) is overexpressed in OCs. Therefore, it is of great interest to investigate whether WT1-specific antibody (Ab) measurements in plasma can serve as a biomarker of anti-OC response, and is of importance in relation to patient prognosis. Peripheral blood samples were obtained from a total of 103 women with ovarian tumors with median being 1 day (range 0–48 days) before operation. WT1 IgG Ab levels were evaluated using enzyme-linked immunosorbent assay (ELISA). Immunohistochemical analysis of WT1 protein expression was performed on OC tissue samples. We found that low-WT1 Ab level in plasma was related to improved survival in patients diagnosed at stages III–IV and grade 3 carcinomas. Positive WT1 protein staining on OC tissue samples had a negative impact on survival in the entire cohort, both overall survival (OS) (P = 0.046) and progression-free survival (PFS) (P = 0.006), but not in the serous OC subtype. Combining WT1 IgG Ab levels and WT1 staining, patients with high-WT1 IgG Ab levels in plasma and positive WT1 protein staining in cancer tissues had shorter survival, with a significant association in PFS (P = 0.016). These results indicated that WT1 Ab measurements in plasma and WT1 staining in tissue specimens could be useful as biomarkers for patient outcome in the high-risk subtypes of OCs for postoperative individualized therapy. BlackWell Publishing Ltd 2014-08 2014-04-08 /pmc/articles/PMC4303158/ /pubmed/24715586 http://dx.doi.org/10.1002/cam4.244 Text en © 2014 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Cancer Research Andersson, Charlotta Oji, Yusuke Ohlson, Nina Wang, Sihan Li, Xingru Ottander, Ulrika Lundin, Eva Sugiyama, Haruo Li, Aihong Prognostic significance of specific anti-WT1 IgG antibody level in plasma in patients with ovarian carcinoma |
title | Prognostic significance of specific anti-WT1 IgG antibody level in plasma in patients with ovarian carcinoma |
title_full | Prognostic significance of specific anti-WT1 IgG antibody level in plasma in patients with ovarian carcinoma |
title_fullStr | Prognostic significance of specific anti-WT1 IgG antibody level in plasma in patients with ovarian carcinoma |
title_full_unstemmed | Prognostic significance of specific anti-WT1 IgG antibody level in plasma in patients with ovarian carcinoma |
title_short | Prognostic significance of specific anti-WT1 IgG antibody level in plasma in patients with ovarian carcinoma |
title_sort | prognostic significance of specific anti-wt1 igg antibody level in plasma in patients with ovarian carcinoma |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303158/ https://www.ncbi.nlm.nih.gov/pubmed/24715586 http://dx.doi.org/10.1002/cam4.244 |
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