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Tumor infiltrating B-cells are increased in prostate cancer tissue

Open access
Woo, Jason R, Liss, Michael A, Muldong, Michelle T, Palazzi, Kerrin, Strasner, Amy, Ammirante, Massimo, Varki, Nissi, Shabaik, Ahmed, Howell, Stephen, Kane, Christopher J, Karin, Michael, Jamieson, Christina AM·2014·Journal of Translational Medicine

Abstract

BACKGROUND: The presence of increased B-cell tumor infiltrating lymphocytes (TILs) was seen in mouse prostate cancer (PCa) but has not been fully documented in human PCa. We, therefore, investigated the density of infiltrating B cells within human PCa utilizing a quantitative computational method. METHODS: Archived radical prostatectomy specimens from 53 patients with known clinical outcome and D'Amico risk category were obtained and immunohistochemically (IHC) stained for the B cell marker, CD20. Slides were reviewed by a genitourinary pathologist who manually delineated the tumoral regions of PCa. Slides were digitally scanned and a computer algorithm quantified the area of CD20 stained B-cells as a measure of B cell density within the outlined regions of prostate cancer (intra-tumoral region), versus extra-tumoral prostate tissue. Correlations were analyzed between B-cell density and demographic and clinical variables, including D'Amico risk groups and disease recurrence. RESULTS: For the entire cohort, the mean intra-tumoral B cell density was higher (3.22 SE = 0.29) than in the extra-tumoral region of each prostatectomy section (2.24, SE = 0.19) (paired t test; P < 0.001). When analyzed according to D'Amico risk group, the intra-tumoral B cell infiltration in low risk (0.0377 vs. 0.0246; p = 0.151) and intermediate risk (0.0260 vs. 0.0214; p = 0.579) patient prostatectomy specimens did not show significantly more B-cells within the PCa tumor. However, patient specimens from the high-risk group (0.0301 vs. 0.0197; p < 0.001) and from those who eventually had PCa recurrence or progression (0.0343 vs. 0.0246; p = 0.019) did show significantly more intra-tumoral CD20+ B-cell staining. Extent of B-cell infiltration in the prostatectomy specimens did not correlate with any other clinical parameters. CONCLUSIONS: Our study shows that higher B-cell infiltration was present within the intra-tumoral PCa regions compared to the extra-tumoral benign prostate tissue regions in prostatectomy sections. For this study we developed a new method to measure B-cells using computer-assisted digitized image analysis. Accurate, consistent quantitation of B-cells in prostatectomy specimens is essential for future clinical trials evaluating the effect of B cell ablating antibodies. The interaction of B-cells and PCa may serve as the basis for new therapeutic targets.

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Metadata

Authors
Woo, J. R., Liss, M. A., Muldong, M. T., Palazzi, K., Strasner, A., Ammirante, M., Varki, N., Shabaik, A., Howell, S., Kane, C. J., Karin, M., & Jamieson, C. A.
Venue
Journal of Translational Medicine
Published
2014-01-30
Volume
12
Issue
1
Pages
30-30
ISSN
1479-5876 (ISSN-L)
OpenAlex
W2157860451
Cited by
180
References
1
FWCI
11.15
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Tumor infiltrating B-cells are increased in prostate cancer tissue. https://app.cochat.ai/papers/10.1186/1479-5876-12-30
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Woo, J. R., Liss, M. A., Muldong, M. T., Palazzi, K., Strasner, A., Ammirante, M., Varki, N., Shabaik, A., Howell, S., Kane, C. J., Karin, M., & Jamieson, C. A. (2014). Tumor infiltrating B-cells are increased in prostate cancer tissue. Journal of Translational Medicine. https://doi.org/10.1186/1479-5876-12-30

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