Skip to Main Content

An official website of the United States government

Principal Investigator
Name
Demetrius Albanes
Degrees
MD
Institution
National Cancer Institute
Position Title
Senior Investigator
Email
About this CDAS Project
Study
PLCO (Learn more about this study)
Project ID
PLCO-1626
Initial CDAS Request Approval
Jul 22, 2024
Title
Associations between vitamin D-related genotypes and prostate and colorectal cancer risk and survival by race/ethnicity in PLCO
Summary
Black men in the US and elsewhere experience higher rates of prostate cancer incidence and mortality compared with White men and those of other races/ethnicities. Similarly, Black men and women experience higher colorectal cancer rates. Vitamin D biochemical status 1) is known to be lower among Black men and women owing to the influence of increased skin pigmentation leading to decreased UVB-stimulated production of 25(OH)-vitamin D in the skin, 2) is associated with risk of prostate and colorectal cancer, 3) is strongly influenced by a few genes and their related polymorphic variants, including those related to vitamin D transport, biosynthesis, and metabolism, and 4) the prevalence of variant alleles in the GC gene encoding the vitamin D-binding protein (DBP) differ in Black versus non-Black individuals. This study will examine vitamin D-related genotypes (including GC, DHCR7, CYP2R1, and CYP24A1), available from the PLCO genome-wide scan, in relation to prostate cancer risk (in men) and colorectal cancer risk (in men and women) by race/ethnicity in order to determine whether higher or lower risks/rates exist for individuals with specific genotypes.
Aims

1. To determine whether, relative to White men and men of other races/ethnicities, increased prostate cancer risk among Black men exists for specific vitamin D-related genotypes, including GC, DHCR7, CYP2R1, and CYP24A1.

2. To determine whether, relative to White men and men of other races/ethnicities, decreased prostate cancer survival among Black men exists for specific vitamin D-related genotypes, including GC, DHCR7, CYP2R1, and CYP24A1.

3. To determine whether, relative to White men and women and those of other races/ethnicities, decreased colorectal cancer risk among Black men and women exists for specific vitamin D-related genotypes, including GC, DHCR7, CYP2R1, and CYP24A1.

4. To determine whether, relative to White men and women and those of other races/ethnicities, decreased colorectal cancer survival among Black men and women exists for specific vitamin D-related genotypes, including GC, DHCR7, CYP2R1, and CYP24A1.

Collaborators

Stephanie J. Weinstein, PhD, Metabolic Epidemiology Branch, DCEG
Kai Yu, PhD, Biostatistics Branch, DCEG