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The prognostic significance of PELP1 expression in invasive breast cancer with emphasis on the ER-positive luminal-like subtype
Breast Cancer Research and Treatment, 06/09/09
Habashy HO et al. - In a trial to explore clinical and biological relevance of proline, glutamate, and leucine rich protein 1 (PELP1) protein expression in a group of consecutive pts (1162 pts) with invasive breast cancers with particular emphasis on its role in the oestrogen receptors (ER)-positive/luminal-like class of tumours, it was shown that PELP1 protein expression is an independent prognostic predictor of shorter breast cancer specific survival (BCSS) and disease-free survival (DFI) in breast cancer and its elevated expression is positively associated with markers of poor outcome. PELP1 appears to have a potential application in assessing clinical outcome of pts with ER-positive breast cancer.
Methods- Transcription functions of ER are influenced by several coregulators such as PELP1.
- This study uses tissue microarrays and immunohistochemistry.
- Increased PELP1 expression is associated with tumours of larger size, higher histological grade, higher mitotic count, and with positive expression of basal cytokeratins (CK) (CK14 and CK5/6), P-cadherin, p53, and MIB1.
- There was an inverse association between PELP1 expression and ER, progesterone (PgR), androgen (AR) receptor, and luminal CK (CK18) expression.
- A significant association between PELP1 expression and shorter BCSS and DFI was found.
- Multivariate Cox hazard analysis showed that PELP1 expression was an independent predictor of shorter BCSS and shorter DFI.
- In the ER-positive/luminal-like group (n=768), PELP1 expression showed similar association with other clinicopathological variables and was an independent predictor of shorter DFI.
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