Ra. Lothe et al., THE APC GENE I1307K VARIANT IS RARE IN NORWEGIAN PATIENTS WITH FAMILIAL AND SPORADIC COLORECTAL OR BREAST-CANCER, Cancer research, 58(14), 1998, pp. 2923-2924
Recently, a T-to-A transversion creating an 8-base mononucleotide trac
t in the APC gene, resulting in substitution of lysine for isoleucine
at codon 1307 (11307K), was found in a subset of Ashkenazi Jews. This
sequence variant was most frequent in colorectal cancer patients with
a positive family history of colorectal cancer. To determine whether t
he 11307K variant plays a role in colorectal or breast cancer predispo
sition in the Norwegian population, we have analyzed blood samples fro
m 210 colorectal cancer patients and 183 breast cancer patients by PCR
and direct sequencing. Thirty-seven of the colorectal cancer patients
had a positive family history of cancer. Among the breast cancer pati
ents, 24 had a family history of colorectal cancer and 75 a family his
tory of breast and/or ovarian cancer. Only one colorectal cancer patie
nt who belonged to a Jewish family was found to carry the A variant. O
ur data show that the 11307K variant is rare in the Norwegian populati
on and should not be viewed as a candidate for susceptibility testing
for colorectal cancer.