Abstract | BACKGROUND: METHODS: We utilised a tissue microarray (TMA) of 530 CaP cores from 168 individual patients and stained for both mir143 and ERK5. These TMAs were scored by a combination of observer and automated methods. RESULTS: We observed a strong inverse relation between ERK5 and mir143, which manifested itself most strongly in the subgroup of 417 cores with non-zero mir143 and ERK5 immunoreactivity, or with only one of mir143 or ERK5 being zero (cc=0.2558 and P<0.0001). Mir143 neither correlate with Gleason scores or prostate-specific antigen levels, nor was it a predictor of disease-specific survival on univariate analysis. CONCLUSION: Although the mechanism for ERK5 activation in CaP remains to be fully elucidated, we have further validated the potential role of mir143 in regulating ERK5 levels in the clinical context. In addition, we demonstrate that the automated counting method for nuclear ERK5 is a clinically useful alterative to observer counting method in patient stratification in the context of ERK5 targeting therapy.
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Authors | I Ahmad, L B Singh, Z H Yang, G Kalna, J Fleming, G Fisher, C Cooper, J Cuzick, D M Berney, H Møller, P Scardino, H Y Leung |
Journal | British journal of cancer
(Br J Cancer)
Vol. 108
Issue 1
Pg. 149-54
(Jan 15 2013)
ISSN: 1532-1827 [Electronic] England |
PMID | 23321517
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Validation Study)
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Chemical References |
- MIRN143 microRNA, human
- MicroRNAs
- Mitogen-Activated Protein Kinase 7
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Topics |
- Gene Expression Regulation
- Humans
- Male
- MicroRNAs
(metabolism)
- Mitogen-Activated Protein Kinase 7
(metabolism)
- Prostatic Neoplasms
(genetics, metabolism)
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