Alternative splicing and the progresterone receptor in breast cancer

  1. Lookup NU author(s)
  2. Dr David Cork
  3. Professor Thomas Lennard
  4. Dr Alison Tyson-Capper
Author(s)Cork DMW, Lennard TWJ, Tyson-Capper AJ
Publication type Review
JournalBreast Cancer Research
Year2008
Volume10
Issue3
Pages207
ISSN (print)1465-5411
ISSN (electronic)1465-542X
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Progesterone receptor status is a marker for hormone responsiveness and disease prognosis in breast cancer. Progesterone receptor negative tumours have generally been shown to have a poorer prognosis than progesterone receptor positive tumours. The observed loss of progesterone receptor could be through a range of mechanisms, including the generation of alternatively spliced progesterone receptor variants that are not detectable by current screening methods. Many progesterone receptor mRNA variants have been described with deletions of various whole, multiple or partial exons that encode differing protein functional domains. These variants may alter the progestin responsiveness of a tissue and contribute to the abnormal growth associated with breast cancer. Absence of specific functional domains from these spliced variants may also make them undetectable or indistinguishable from full length progesterone receptor by conventional antibodies. A comprehensive investigation into the expression profile and activity of progesterone receptor spliced variants in breast cancer is required to advance our understanding of tumour hormone receptor status. This, in turn, may aid the development of new biomarkers of disease prognosis and improve adjuvant treatment decisions.
Current Medicine Group Ltd.
URLhttp://dx.doi.org/10.1186/bcr2097
DOI10.1186/bcr2097
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