Herceptin resistance in HER2-moderately expressed breast cancer

<p>HER2 overexpression occurs in approximately 15-20% of all breast cancers and is associated with poor prognosis. The development of Herceptin, a monoclonal antibody against HER2, has been significant in prolonging survival of these patients. Herceptin is less efficient in patients who do not...

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Egile Nagusiak: Kerry, J, Jonathan Kerry
Beste egile batzuk: Kong, A
Formatua: Thesis
Hizkuntza:English
Argitaratua: 2012
Gaiak:
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author Kerry, J
Jonathan Kerry
author2 Kong, A
author_facet Kong, A
Kerry, J
Jonathan Kerry
author_sort Kerry, J
collection OXFORD
description <p>HER2 overexpression occurs in approximately 15-20% of all breast cancers and is associated with poor prognosis. The development of Herceptin, a monoclonal antibody against HER2, has been significant in prolonging survival of these patients. Herceptin is less efficient in patients who do not overexpress HER2, so-called HER2-negative, such that they are not eligible for treatment with this drug. An incomplete understanding of Herceptin action and HER2 classification means that these patients may unnecessarily be being denied targeted therapy. In this thesis I show that an inability of Herceptin to maintain decreased HER3 and AKT activation in a subset of HER2-negative breast cancer cell lines (those that are HER2 2+, or HER2-moderately expressed) is responsible for reduced response. Surprisingly HER3 activation may also have a role in propagating the effects of Herceptin in these cells, making this receptor a central player. This study also shows that HER2-moderately expressed cells can rely heavily on ADAM-mediated ErbB receptors for normal survival and that targeting these by means of ADAM or tyrosine kinase inhibitors may present a better therapeutic option for these patients.</p>
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spelling oxford-uuid:349db701-77e7-477c-b2ba-eee10cdb5f822024-12-07T12:53:21ZHerceptin resistance in HER2-moderately expressed breast cancerThesishttp://purl.org/coar/resource_type/c_db06uuid:349db701-77e7-477c-b2ba-eee10cdb5f82OncologyEnglish2012Kerry, JJonathan KerryKong, A<p>HER2 overexpression occurs in approximately 15-20% of all breast cancers and is associated with poor prognosis. The development of Herceptin, a monoclonal antibody against HER2, has been significant in prolonging survival of these patients. Herceptin is less efficient in patients who do not overexpress HER2, so-called HER2-negative, such that they are not eligible for treatment with this drug. An incomplete understanding of Herceptin action and HER2 classification means that these patients may unnecessarily be being denied targeted therapy. In this thesis I show that an inability of Herceptin to maintain decreased HER3 and AKT activation in a subset of HER2-negative breast cancer cell lines (those that are HER2 2+, or HER2-moderately expressed) is responsible for reduced response. Surprisingly HER3 activation may also have a role in propagating the effects of Herceptin in these cells, making this receptor a central player. This study also shows that HER2-moderately expressed cells can rely heavily on ADAM-mediated ErbB receptors for normal survival and that targeting these by means of ADAM or tyrosine kinase inhibitors may present a better therapeutic option for these patients.</p>
spellingShingle Oncology
Kerry, J
Jonathan Kerry
Herceptin resistance in HER2-moderately expressed breast cancer
title Herceptin resistance in HER2-moderately expressed breast cancer
title_full Herceptin resistance in HER2-moderately expressed breast cancer
title_fullStr Herceptin resistance in HER2-moderately expressed breast cancer
title_full_unstemmed Herceptin resistance in HER2-moderately expressed breast cancer
title_short Herceptin resistance in HER2-moderately expressed breast cancer
title_sort herceptin resistance in her2 moderately expressed breast cancer
topic Oncology
work_keys_str_mv AT kerryj herceptinresistanceinher2moderatelyexpressedbreastcancer
AT jonathankerry herceptinresistanceinher2moderatelyexpressedbreastcancer