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Proliferating cell nuclear antigen (PCNA) immunostaining--a prognostic factor in ovarian cancer?

The measurement of tumour cell proliferation is becoming increasingly recognised in defining prognostic groups. Proliferating cell nuclear antigen (PCNA) immunolocalisation can be used as an index of cell proliferation and may define the extent of departure from normal growth control. The monoclonal...

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Autores principales: Thomas, H., Nasim, M. M., Sarraf, C. E., Alison, M. R., Love, S., Lambert, H. E., Price, P.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033602/
https://www.ncbi.nlm.nih.gov/pubmed/7841053
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author Thomas, H.
Nasim, M. M.
Sarraf, C. E.
Alison, M. R.
Love, S.
Lambert, H. E.
Price, P.
author_facet Thomas, H.
Nasim, M. M.
Sarraf, C. E.
Alison, M. R.
Love, S.
Lambert, H. E.
Price, P.
author_sort Thomas, H.
collection PubMed
description The measurement of tumour cell proliferation is becoming increasingly recognised in defining prognostic groups. Proliferating cell nuclear antigen (PCNA) immunolocalisation can be used as an index of cell proliferation and may define the extent of departure from normal growth control. The monoclonal antibody PC10 stains PCNA in archival paraffin-embedded tissue. This study investigates its potential as a prognostic marker in early and advanced ovarian cancer. A three-stage immunoperoxidase technique was developed to detect the monoclonal antibody PC10. Archival paraffin-embedded tissue from 19 stage I ovarian tumours (13 malignant and six borderline) and 79 advanced (stage IIb-IV) ovarian tumours (patients entered into the Third North-West Thames Ovarian Cancer Trial) was immunostained with PC10. PC10 immunostaining was performed successfully in 91.8% of cases. The PC10 labelling index (PC10 LI) ranged from 1.5% to 88% with a mean value of 47.4%. Stage I borderline tumours had significantly lower PCNA labelling indexes than stage I malignant tumours (P < 0.048). In advanced disease there was an inverse correlation between PC10 and overall survival, and in those patients who underwent good debulking surgery (37 patients with disease < 2 cm diameter) a low PC10 value (< 36.5%) correlated with improved survival (log-rank trend test for survival, chi 2 = 5.75, P = 0.017). PCNA immunostaining defines a good prognostic subgroup in adequately debulked patients with ovarian cancer. IMAGES:
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spelling pubmed-20336022009-09-10 Proliferating cell nuclear antigen (PCNA) immunostaining--a prognostic factor in ovarian cancer? Thomas, H. Nasim, M. M. Sarraf, C. E. Alison, M. R. Love, S. Lambert, H. E. Price, P. Br J Cancer Research Article The measurement of tumour cell proliferation is becoming increasingly recognised in defining prognostic groups. Proliferating cell nuclear antigen (PCNA) immunolocalisation can be used as an index of cell proliferation and may define the extent of departure from normal growth control. The monoclonal antibody PC10 stains PCNA in archival paraffin-embedded tissue. This study investigates its potential as a prognostic marker in early and advanced ovarian cancer. A three-stage immunoperoxidase technique was developed to detect the monoclonal antibody PC10. Archival paraffin-embedded tissue from 19 stage I ovarian tumours (13 malignant and six borderline) and 79 advanced (stage IIb-IV) ovarian tumours (patients entered into the Third North-West Thames Ovarian Cancer Trial) was immunostained with PC10. PC10 immunostaining was performed successfully in 91.8% of cases. The PC10 labelling index (PC10 LI) ranged from 1.5% to 88% with a mean value of 47.4%. Stage I borderline tumours had significantly lower PCNA labelling indexes than stage I malignant tumours (P < 0.048). In advanced disease there was an inverse correlation between PC10 and overall survival, and in those patients who underwent good debulking surgery (37 patients with disease < 2 cm diameter) a low PC10 value (< 36.5%) correlated with improved survival (log-rank trend test for survival, chi 2 = 5.75, P = 0.017). PCNA immunostaining defines a good prognostic subgroup in adequately debulked patients with ovarian cancer. IMAGES: Nature Publishing Group 1995-02 /pmc/articles/PMC2033602/ /pubmed/7841053 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Thomas, H.
Nasim, M. M.
Sarraf, C. E.
Alison, M. R.
Love, S.
Lambert, H. E.
Price, P.
Proliferating cell nuclear antigen (PCNA) immunostaining--a prognostic factor in ovarian cancer?
title Proliferating cell nuclear antigen (PCNA) immunostaining--a prognostic factor in ovarian cancer?
title_full Proliferating cell nuclear antigen (PCNA) immunostaining--a prognostic factor in ovarian cancer?
title_fullStr Proliferating cell nuclear antigen (PCNA) immunostaining--a prognostic factor in ovarian cancer?
title_full_unstemmed Proliferating cell nuclear antigen (PCNA) immunostaining--a prognostic factor in ovarian cancer?
title_short Proliferating cell nuclear antigen (PCNA) immunostaining--a prognostic factor in ovarian cancer?
title_sort proliferating cell nuclear antigen (pcna) immunostaining--a prognostic factor in ovarian cancer?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033602/
https://www.ncbi.nlm.nih.gov/pubmed/7841053
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