Gene expression profiling of prostate tissue identifies chromatin regulation as a potential link between obesity and lethal prostate cancer Journal Article


Authors: Ebot, E. M.; Gerke, T.; Labbé, D. P.; Sinnott, J. A.; Zadra, G.; Rider, J. R.; Tyekucheva, S.; Wilson, K. M.; Kelly, R. S.; Shui, I. M.; Loda, M.; Kantoff, P. W.; Finn, S.; Vander Heiden, M. G.; Brown, M.; Giovannucci, E. L.; Mucci, L. A.
Article Title: Gene expression profiling of prostate tissue identifies chromatin regulation as a potential link between obesity and lethal prostate cancer
Abstract: BACKGROUND: Obese men are at higher risk of advanced prostate cancer and cancer-specific mortality; however, the biology underlying this association remains unclear. This study examined gene expression profiles of prostate tissue to identify biological processes differentially expressed by obesity status and lethal prostate cancer. METHODS: Gene expression profiling was performed on tumor (n = 402) and adjacent normal (n = 200) prostate tissue from participants in 2 prospective cohorts who had been diagnosed with prostate cancer from 1982 to 2005. Body mass index (BMI) was calculated from the questionnaire immediately preceding cancer diagnosis. Men were followed for metastases or prostate cancer–specific death (lethal disease) through 2011. Gene Ontology biological processes differentially expressed by BMI were identified using gene set enrichment analysis. Pathway scores were computed by averaging the signal intensities of member genes. Odds ratios (ORs) for lethal prostate cancer were estimated with logistic regression. RESULTS: Among 402 men, 48% were healthy weight, 31% were overweight, and 21% were very overweight/obese. Fifteen gene sets were enriched in tumor tissue, but not normal tissue, of very overweight/obese men versus healthy-weight men; 5 of these were related to chromatin modification and remodeling (false-discovery rate < 0.25). Patients with high tumor expression of chromatin-related genes had worse clinical characteristics (Gleason grade > 7, 41% vs 17%; P = 2 × 10–4) and an increased risk of lethal disease that was independent of grade and stage (OR, 5.26; 95% confidence interval, 2.37-12.25). CONCLUSIONS: This study improves our understanding of the biology of aggressive prostate cancer and identifies a potential mechanistic link between obesity and prostate cancer death that warrants further study. Cancer 2017;123:4130–4138. © 2017 American Cancer Society. © 2017 American Cancer Society
Keywords: gene expression; obesity; prostate cancer; body mass index; chromatin modification; chromatin remodeling; prostate cancer–specific mortality
Journal Title: Cancer
Volume: 123
Issue: 21
ISSN: 0008-543X
Publisher: Wiley Blackwell  
Date Published: 2017-11-01
Start Page: 4130
End Page: 4138
Language: English
DOI: 10.1002/cncr.30831
PROVIDER: scopus
PUBMED: 28700821
PMCID: PMC5802874
DOI/URL:
Notes: Article -- Export Date: 1 November 2017 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Philip Wayne Kantoff
    197 Kantoff