EXPRESSION OF THE CEA GENE FAMILY MEMBERS NCA-50 90 AND NCA-160 (CD66) IN CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIAS (ALLS) AND IN CELL-LINES OF B-CELL ORIGIN/
H. Hanenberg et al., EXPRESSION OF THE CEA GENE FAMILY MEMBERS NCA-50 90 AND NCA-160 (CD66) IN CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIAS (ALLS) AND IN CELL-LINES OF B-CELL ORIGIN/, Leukemia, 8(12), 1994, pp. 2127-2133
The carcinoembryonic antigen (CEA) and the classical nonspecific cross
-reacting antigens (NCAs) belong to the CEA gene family which is part
of the immunoglobulin superfamily. In normal hematopoiesis, CEA gene f
amily members (CGMs) have only been reported on cells of myeloid and m
onocytic origin. In the present study, we analyzed 62 childhood acute
lymphoblastic leukemias (ALLs) and seven surface immunoglogulin positi
ve (sig+) B-cell lines for the expression of the CEA family members CE
A, NCA-50/90, NCA-95, NCA-160, CGM1 and CGM7. We demonstrated that mem
bers of the CEA family were present in 76% of childhood ALLs of B- and
T-cell origin. In ALLs of B-cell origin, 82% of the samples expressed
at least one CEA subgroup member: 38% NCA-50/90 (CD66c), 31% NCA-160
(CD66a), and 13% both. Six of seven B-cell lines solely expressed NCA-
160. In seven ALL of T-cell origin, sole NCA-160 expression was presen
t in 29% of the cases. CEA and CGM1 were not expressed in childhood AL
Ls or in the sIg+ B-cell lines. In 15 ALLs and seven B-cell lines whic
h could be analyzed for CGM7 expression, the antigen was not detected.
NCA-95 was not expressed in 91% of the B-lineage ALLs, in T-lineage A
LLs and in the B-cell lines. However, five B-lineage ALLs showed confl
icting data on the binding patterns of two, on leukocytes specifically
NCA-95 recognizing antibodies suggesting either expression of unknown
forms of NCA-95 or NCA-50/90 or of a yet unknown member of the CEA fa
mily in these ALL cells. The expression of CEA subgroup members in chi
ldhood ALL cells might have prognostic impacts, as an inverse correlat
ion exists between NCA expression on leukemic blasts and the risk fact
or white blood count at diagnosis.