Reduced infiltration of class A scavenger receptor positive antigen-presenting cells is associated with prostate cancer progression

• Published in: Cancer research (Chicago, Ill.) Ill.), 2004-03, Vol.64 (6), p.2076-2082
• Main Authors: GUANG YANG, ADDAI, Josephine, TIAN, Wei-Hua, FROLOV, Anna, WHEELER, Thomas M, THOMPSON, Timothy C
• Format: Article
• Language: English
• Subjects: Aged; Antigen-Presenting Cells - immunology; Antigens, CD - metabolism; Antigens, Differentiation, Myelomonocytic - metabolism; Antineoplastic agents; Biological and medical sciences; CD36 Antigens - metabolism; Dendritic Cells - immunology; Dendritic Cells - metabolism; Dendritic Cells - pathology; Disease Progression; Humans; Macrophages - immunology; Macrophages - metabolism; Macrophages - pathology; Male; Medical sciences; Middle Aged; Pharmacology. Drug treatments; Prognosis; Prostatectomy; Prostatic Intraepithelial Neoplasia - metabolism; Prostatic Intraepithelial Neoplasia - pathology; Prostatic Neoplasms - metabolism; Prostatic Neoplasms - pathology; S100 Proteins - metabolism; Scavenger Receptors, Class A; Tumors
• ISSN: 0008-5472; 1538-7445
• DOI: 10.1158/0008-5472.CAN-03-4072

The class A macrophage scavenger receptor (SR-A) is expressed in antigen presenting cells and is involved in host immune responses. Germ-line mutation of this gene has been associated with increased risk of human prostate cancer. However, there is little known about its expression in normal or neoplastic human prostate tissues. Double immunofluorescent labeling with monoclonal antibodies to SR-A and specific macrophage and dendritic cell markers was used to identify cells expressing SR-A in human prostate tissues. SR-A immunohistochemical staining was performed on paraffin sections of normal prostate, prostatic intraepithelial neoplasia (PIN) lesions, and prostate cancers from radical prostatectomy specimens. SR-A was expressed in a subset of macrophages and dendritic cells that infiltrated prostatic tissues. The majority of SR-A-positive cells coexpressed CD68, and a relatively low percentage expressed S100 protein. The number of SR-A-positive cells was significantly increased in PIN as compared with normal prostatic tissue (P = 0.0176). In contrast, the number of SR-A-positive cells decreased with tumor progression. A lower SR-A-positive cell density was associated with higher clinical stage (rho = -0.26; P = 0.0234). Inverse associations were also found between SR-A density and positive lymph nodes (rho = -0.23; P = 0.0437), tumor size (rho = -0.31; P = 0.0100) and preoperative PSA levels (rho = -0.32; P = 0.0057). SR-A density is a significant predictor of disease-free survival after surgery univariately (P = 0.0003), as well as multivariately, adjusted for known clinical and pathological markers including preoperative prostate-specific antigen, clinical stage, Gleason score, surgical margin, extraprostatic extension, and seminal vesicle invasion, as well as lymph node metastasis (P = 0.0021). The preferential accumulation of SR-A-positive cells in PIN suggests a role for SR-A in the APC response to early malignancy. A reduction in the number of SR-A-positive cells demarcates tumor progression as indicated by clinical and pathological correlations. Our results additionally indicate that systematic measurement of SR-A density is a strong prognostic marker for clinical outcome after surgery.