Sa. Chappell et al., A mutation in the c-myc-IRES leads to enhanced internal ribosome entry in multiple myeloma: A novel mechanism of oncogene de-regulation, ONCOGENE, 19(38), 2000, pp. 4437-4440
The 5' untranslated region of the proto-oncogene c-myc contains an internal
ribosome entry segment (IRES) (Nanbru ct nl,, 1997; Stoneley ct al., 1998)
and thus c-myc protein synthesis can be initiated by a cap-independent as
well as a cap-dependent mechanism (Stoneley ct al., 2000), In cell lines de
rived from patients with multiple myeloma (RIM) there is aberrant translati
onal regulation of c-myc and this correlates with a C-T mutation in the c-m
yc-IRES (Paulin ct nl,, 1996), RNA derived from the mutant IRES displays en
hanced binding of protein factors (Paulin ct nl,, 1998), Here we show that
the same mutation is present in 42% of bone marrow samples obtained from pa
tients with MM, but was not present in any of 21 controls demonstrating a s
trong correlation between this mutation and the disease. In a tissue cultur
e based assay, the mutant version of the c-myc-IRES was more active in all
cell types tested, but showed the greatest activity in a cell line derived
from a patient with MM. Our data demonstrate that a single mutation in the
c-myc-IRES is sufficient to cause enhanced initiation of translation via in
ternal ribosome entry and represents a novel mechanism of oncogenesis.