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Tumor expression of adiponectin receptor 2 and lethal prostate cancer.

Authors :
Rider, Jennifer R.
Fiorentino, Michelangelo
Kelly, Rachel
Gerke, Travis
Jordahlz, Kristina
Sinnott, Jennifer A.
Giovannucci, Edward L.
Loda, Massimo
Mucci, Lorelei A.
Finn, Stephen
Source :
Carcinogenesis; Jun2015, Vol. 36 Issue 6, p639-647, 9p, 1 Diagram, 3 Charts, 1 Graph
Publication Year :
2015

Abstract

To investigate the role of adiponectin receptor 2 (AdipoR2) in aggressive prostate cancer we used immunohistochemistry to characterize AdipoR2 protein expression in tumor tissue for 866 men with prostate cancer from the Physicians’ Health Study and the Health Professionals Follow-up Study. AdipoR2 tumor expression was not associated with measures of obesity, pathological tumor stage or prostate-specific antigen (PSA) at diagnosis. However, AdipoR2 expression was positively associated with proliferation as measured by Ki-67 expression quartiles (P-trend < 0.0001), with expression of fatty acid synthase (P-trend = 0.001), and with two measures of angiogenesis (P-trend < 0.1). An inverse association was observed with apoptosis as assessed by the TUNEL assay (P-trend = 0.006). Using Cox proportional hazards regression and controlling for age at diagnosis, Gleason score, year of diagnosis category, cohort and baseline BMI, we identified a statistically significant trend for the association between quartile of AdipoR2 expression and lethal prostate cancer (P-trend = 0.02). The hazard ratio for lethal prostate cancer for the two highest quartiles, as compared to the two lowest quartiles, of AdipoR2 expression was 1.9 (95% confidence interval [CI]: 1.2–3.0). Results were similar when additionally controlling for categories of PSA at diagnosis and Ki-67 expression quartiles. These results strengthen the evidence for the role of AdipoR2 in prostate cancer progression. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01433334
Volume :
36
Issue :
6
Database :
Complementary Index
Journal :
Carcinogenesis
Publication Type :
Academic Journal
Accession number :
115974356
Full Text :
https://doi.org/10.1093/carcin/bgv048