The mRNA Expression of Inhibitors of DNA Binding-1 and -2 Is Associated with Advanced Tumour Stage and Adverse Clinical Outcome in Human Breast Cancer
- 1The London Breast Institute, Princess Grace Hospital, London, UK
- 2Department of Breast Surgery, St. George's Hospital and Medical School, University of London, London, U.K
- 3Metastasis and Angiogenesis Research Group, Department of Surgery, School of Medicine, Cardiff University, Cardiff, Wales, U.K.
- Correspondence to: Professor Kefah Mokbel, London Breast Institute, the Princess Grace Hospital, 45 Nottingham Place, London W1U 5NY, U.K. E-mail: kefahmokbel{at}hotmail.com
Abstract
Inhibitors of DNA binding (ID) are known to have a role in embryogenesis and oncogenesis. In this study, we analyzed the role of ID1 and ID2 in breast cancer, by assessing associations of mRNA expression with clinicopathological parameters. Materials and Methods: Breast cancer tissues (n=152) and adjacent normal tissues (n=31) underwent reverse transcription and quantitative- polymerase chain reaction (qPCR). Transcript levels were correlated with clinicopathological data. Results: Patients who were disease–free had significantly lower ID1 mRNA expression than all other patients (p=0.0033). Higher expression was associated with worse disease-free (p=0.001) and overall survival (p=0.02). ID2 expression was directly associated with the Nottingham Prognostic Index (NPI) (NPI 2 vs. 3; p=0.0062) and worsening clinical outcome (disease-free vs. mortality: p=0.0004), and with worse disease-free (p=0.01) and overall survival (p=0.005). Conclusion: Our findings are suggestive of a role for ID1 and ID2 in human breast cancer as possible prognostic markers and therapeutic targets meriting further validating investigations, by immunohistochemistry and mechanistic studies.
- Inhibitor of differentiation
- inhibitor of DNA binding
- ID1
- ID2
- qPCR
- breast cancer
- helix-loop-helix
- cell cycle
- Received January 15, 2013.
- Revision received April 4, 2013.
- Accepted April 5, 2013.
- Copyright© 2013 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved







