Calcium-Binding Proteins S100A8 and S100A9 as Novel Diagnostic Markers in Human Prostate Cancer
Open Access
- 15 July 2005
- journal article
- Published by American Association for Cancer Research (AACR) in Clinical Cancer Research
- Vol. 11 (14), 5146-5152
- https://doi.org/10.1158/1078-0432.ccr-05-0352
Abstract
Purpose: S100 proteins comprise a family of calcium-modulated proteins that have recently been associated with epithelial tumors. We examined the expression of two members of this family, S100A8 and S100A9, together with the S100 receptor RAGE (receptor for advanced glycation end products) in human prostate adenocarcinomas and in prostatic intraepithelial neoplasia.Keywords
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This publication has 43 references indexed in Scilit:
- S100 proteins in mouse and man: from evolution to function and pathology (including an update of the nomenclature)Biochemical and Biophysical Research Communications, 2004
- S100A9 expression in invasive ductal carcinoma of the breast: S100A9 expression in adenocarcinoma is closely associated with poor tumour differentiationEuropean Journal of Cancer, 2004
- Gleason grading and prognostic factors in carcinoma of the prostateLaboratory Investigation, 2004
- S100P Stimulates Cell Proliferation and Survival via Receptor for Activated Glycation End Products (RAGE)Online Journal of Public Health Informatics, 2004
- Expression of MRP14 gene is frequently down-regulated in Chinese human esophageal cancerCell Research, 2004
- Gene Expression Signature of Fibroblast Serum Response Predicts Human Cancer Progression: Similarities between Tumors and WoundsPLoS Biology, 2004
- Cancer Statistics, 2003CA: A Cancer Journal for Clinicians, 2003
- Keratinocyte-Specific Onset of Serine Protease BSSP Expression in Experimental CarcinogenesisJournal of Investigative Dermatology, 2001
- Report of the sixth international workshop on human chromosome 1 mapping 2000Cytogenetic and Genome Research, 2001
- Epidermal and dermal distribution of a myelomonocytic antigen (L1) shared by epithelial cells in various inflammatory skin diseasesJournal of the American Academy of Dermatology, 1986