The expression of HLA class I molecules and complement regulatory proteins in ovarian cancer

Over recent decades, translational ovarian cancer research has been impeded by its underappreciated molecular heterogeneity and five-year survival has remained poor. One strategy for addressing this problem is to search for molecular biomarkers that can better inform the development and targeting of...

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Main Author: Rolland, Philip
Format: Thesis (University of Nottingham only)
Language:English
Published: 2008
Subjects:
Online Access:https://eprints.nottingham.ac.uk/10600/
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author Rolland, Philip
author_facet Rolland, Philip
author_sort Rolland, Philip
building Nottingham Research Data Repository
collection Online Access
description Over recent decades, translational ovarian cancer research has been impeded by its underappreciated molecular heterogeneity and five-year survival has remained poor. One strategy for addressing this problem is to search for molecular biomarkers that can better inform the development and targeting of novel treatments. The aim of this thesis was to construct and validate a tissue microarray of ovarian cancer cases and to survey the expression and prognostic capabilities of immunological molecular markers: specifically HLA class I and the membrane bound complement regulatory proteins CD46, CD55 and CD59. These are central to the efficacy of certain immunotherapies and while they have been shown to have prognostic power in breast and colorectal cancer, they have been investigated less in ovarian cancer. Five copies of a tissue microarray representing 339 cases of ovarian cancer which presented to Derby City General Hospital between 1982 and 1997 were made. The array was stained for CK7, CK20, CA125, CEA, p53 and Bcl-2 following a standard immunohistochemical protocol. A linked clinical database was adapted and assessed for data consistency and subsequently used to analyse the prognostic and clinicopathological associations of the expression data. The array was then stained for HLA class I, B2microglobulin and CD59 using commercial antibodies and for CD55 and CD46 using in-house antibodies. Retained expression of HLA class I molecules independently predicted improved prognosis. High expression of CD55 and CD59 were associated with worse prognosis, though not independently of other factors. CD55 expression was more widespread than previously appreciated. This thesis describes the discovery of a new independent marker of prognosis which suggests that immunoediting occurs in ovarian cancer, describes the distribution of markers known to have a negative impact on immunotherapy in ovarian cancer in a large series for the first time and documents the production of a valuable resource for future studies.
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spelling nottingham-106002025-02-28T11:08:53Z https://eprints.nottingham.ac.uk/10600/ The expression of HLA class I molecules and complement regulatory proteins in ovarian cancer Rolland, Philip Over recent decades, translational ovarian cancer research has been impeded by its underappreciated molecular heterogeneity and five-year survival has remained poor. One strategy for addressing this problem is to search for molecular biomarkers that can better inform the development and targeting of novel treatments. The aim of this thesis was to construct and validate a tissue microarray of ovarian cancer cases and to survey the expression and prognostic capabilities of immunological molecular markers: specifically HLA class I and the membrane bound complement regulatory proteins CD46, CD55 and CD59. These are central to the efficacy of certain immunotherapies and while they have been shown to have prognostic power in breast and colorectal cancer, they have been investigated less in ovarian cancer. Five copies of a tissue microarray representing 339 cases of ovarian cancer which presented to Derby City General Hospital between 1982 and 1997 were made. The array was stained for CK7, CK20, CA125, CEA, p53 and Bcl-2 following a standard immunohistochemical protocol. A linked clinical database was adapted and assessed for data consistency and subsequently used to analyse the prognostic and clinicopathological associations of the expression data. The array was then stained for HLA class I, B2microglobulin and CD59 using commercial antibodies and for CD55 and CD46 using in-house antibodies. Retained expression of HLA class I molecules independently predicted improved prognosis. High expression of CD55 and CD59 were associated with worse prognosis, though not independently of other factors. CD55 expression was more widespread than previously appreciated. This thesis describes the discovery of a new independent marker of prognosis which suggests that immunoediting occurs in ovarian cancer, describes the distribution of markers known to have a negative impact on immunotherapy in ovarian cancer in a large series for the first time and documents the production of a valuable resource for future studies. 2008 Thesis (University of Nottingham only) NonPeerReviewed application/pdf en arr https://eprints.nottingham.ac.uk/10600/1/THESIS_ROLLAND_%28ET2%29.pdf Rolland, Philip (2008) The expression of HLA class I molecules and complement regulatory proteins in ovarian cancer. DM thesis, University of Nottingham. Human Leukocyte Antigen Immune editing Immunotherapy Tissue Microarray TMA
spellingShingle Human Leukocyte Antigen
Immune editing
Immunotherapy
Tissue Microarray
TMA
Rolland, Philip
The expression of HLA class I molecules and complement regulatory proteins in ovarian cancer
title The expression of HLA class I molecules and complement regulatory proteins in ovarian cancer
title_full The expression of HLA class I molecules and complement regulatory proteins in ovarian cancer
title_fullStr The expression of HLA class I molecules and complement regulatory proteins in ovarian cancer
title_full_unstemmed The expression of HLA class I molecules and complement regulatory proteins in ovarian cancer
title_short The expression of HLA class I molecules and complement regulatory proteins in ovarian cancer
title_sort expression of hla class i molecules and complement regulatory proteins in ovarian cancer
topic Human Leukocyte Antigen
Immune editing
Immunotherapy
Tissue Microarray
TMA
url https://eprints.nottingham.ac.uk/10600/