U. Latza et al., CD30 ANTIGEN IN EMBRYONAL CARCINOMA AND EMBRYOGENESIS AND RELEASE OF THE SOLUBLE MOLECULE, The American journal of pathology, 146(2), 1995, pp. 463-471
The expression, serological detection, and possible functional role of
the CD30 antigen in Hodgkin's disease and anaplastic large cell lymph
oma is well documented. In embryonal carcinoma (EC), the expression of
this cytokine receptor has been demonstrated only by immunohistology.
Because the CD30 monoclonal antibody Ki-1 was found to cross-react wi
th an unrelated molecule, we examined by in situ hybridization testicu
lar germ cell neoplasms for the presence of CD30-specific transcripts.
CD30 mRNA was detectable in the tumor cells of 9 of 9 cases of EC or
mixed germ cell tumors with an EC component but in no other nonlymphoi
d tumors. Thus, the CD30 transcript expression pattern proved to be id
entical to the immunostaining pattern seen with the CD30-specific mono
clonal antibody Ber-H2. By Northern blot analysis, CD30 transcripts co
uld be demonstrated in the EC cell line Tera-2. Employing a highly sen
sitive second generation sandwich enzyme-linked immunosorbent assay, w
e could detect the soluble CD30 molecule in 8 of 8 sera from patients
with a diagnosis of EC but not in 8 of 10 sera from patients with othe
r testicular germ cell tumors. In fetal tissue, no CD30-expressing ger
m cells or epithelial cells could be observed. Thus, the cellularly ex
pressed CD30 molecule appears to represent a real tumor marker for tes
ticular neoplasms of EC type. Moreover, the serum levels of soluble CD
30 antigen seem to be a promising parameter for monitoring patients wi
th EC.