Xf. Wu et al., D-2 dopamine receptor gene polymorphisms among African-Americans and Mexican-Americans: A lung cancer case-control study, CANC EPID B, 9(10), 2000, pp. 1021-1026
Recent research suggests that variant alleles (A1 and B1) of the DRD2 gene
play a role in determining smoking status. However, no studies have evaluat
ed these variant alleles in African-Americans and Mexican-Americans. The pr
imary objective of this study, therefore, was to test the hypothesis that e
ver smokers in these ethnic groups are more likely than never smokers to ha
ve the DRD2 alleles associated with tobacco use (A1 and B1), Furthermore, b
ecause of a predicted higher prevalence of smokers in a family because of t
he patterns of inheritance of the genotypes associated with tobacco use, we
also anticipated that individuals with these at-risk DRD2 alleles would be
more likely to have a family history of smoking-related cancers. Because o
ther inherited genetic variants may interact with smoking on cancer risk, w
e also hypothesized that this association might differ between cancer patie
nts and control subjects. PCR was used to perform genotyping on peripheral
WBC DNA from 140 lung cancer patients (43 Mexican-Americans and 97 African-
Americans) and 222 age-, sex-, and ethnicity-matched controls (111 Mexican-
Americans and 111 African-Americans). A personal family history was obtaine
d from each participant. There were no statistically significant difference
s in the distribution of the DRD2 genotypes between cases and controls, alt
hough the frequency of the B1 genotype significantly differed by ethnicity
(P = 0.002 for controls and P = 0.001 for cases). The DRD2 genotypes and sm
oking status showed a correlation among Mexican-American controls, although
not among African-American controls. The cigarette pack-years in control s
ubjects for the two ethnic groups combined were 30.8, 21.9, and 18.6 for th
e A1A1, A1A2, and A2A2 genotypes and 36.5, 20.8, and 18.5 for the B1B1, B1B
2, and B2B2 genotypes, respectively. Similar trends were found for the numb
er of cigarettes smoked per day among control subjects. From the standpoint
of polymorphisms, however, there was a borderline significantly increased
(3.6 times greater) frequency of smoking-related cancers among the first-de
gree relatives of case subjects with an A1 allele than among those without
an A1 allele, There was also an elevated (1.8 times greater) frequency of s
moking-related cancer among first-degree relatives of case subjects with a
B1 allele compared with patients without a B1 allele, but this finding was
not statistically significant. This phenomenon was not observed among contr
ol subjects. We noted a trend toward interaction of DRD2 A1 genotypes and c
ase status for increased risk of smoking-related cancer among first-degree
relatives. These findings suggest that the variant DRD2 genotypes are assoc
iated with a greater likelihood to smoke and a greater smoking intensity, a
s well as with a familial aggregation of smoking-related cancers. However,
a large study is needed to confirm this finding.