Grant Details
Grant Number: |
5R01CA133891-05 Interpret this number |
Primary Investigator: |
Giovannucci, Edward |
Organization: |
Harvard School Of Public Health |
Project Title: |
Energy Balance-Related Hormones & Prostate Cancer Incidence & Progression |
Fiscal Year: |
2012 |
Abstract
Abstract
Recent evidence has confirmed that positive energy balance, as estimated by obesity, strongly influences
prostate carcinogenesis. However, the complexity of how energy balance influences, and is influenced, by
various metabolic hormones and sympathetic nervous system activity (SNS) adds considerable complexity to
the role of energy balance for this cancer. Further, the influences of energy balance may differ for prostate
cancer incidence and progression. A third complicating factor is that there may be distinct etiologies for early-
onset and late-onset prostate cancers. We propose three distinct patterns, suggested by our preliminary data
and other studies, whereby energy balance related variables influence prostate cancer:
Pattern 1: Metabolic alterations associated with obesity and lack of physical activity, including high insulin and
leptin, and low adiponectin levels, increase risk of prostate cancer progression. Further, the low testosterone
levels associated with obesity may contribute to more poorly differentiated cancers and thus a worse
prognosis.
Pattern 2: Higher insulin-like growth factor (IGF-1) levels influence progression of well- to moderately-well
differentiated prostate cancers, whereas cancers that have molecular alterations in the IGF-1 signaling
pathway and hence upregulated IGF-1 signaling are relatively unresponsive to circulating IGF-1 levels.
Pattern 3: Younger men with an inherent metabolic phenotype related to SNS activity that disassociates high
energy intake from weight gain and which is associated with chronic prostatitis/chronic pelvic pain syndrome
prostatitis are at increased risk of prostate cancer.
We will address these three patterns whereby energy balance may influence prostate cancer risk in the Health
Professionals Follow-up Study (HPFS), a cohort of the 47,000 men free of cancer at baseline in 1986. We
project 6,085 new cases of prostate cancer by 2010, including 668 fatal cases, with tumor blocks from over
1,900 prostatectomy cases. The sources of the exposure data in the HPFS are questionnaire, including diet,
anthropometric measures, activity, medication use, and plasma samples. The outcome data will be based on
(1) medical record and pathology report review, and (2) tissue block markers that correlate with disease
progression. Stratified analysis and multivariate analysis will be used to control for confounding factors. Our
ultimate goal is to better understand how body weight, and related dietary and other modifiable factors,
influence prostate carginogenesis at various stages.
Publications
None