N. Baou et al., Evidence for a selective loss of somatostatin receptor subtype expression in male germ cell tumors of seminoma type, CARCINOGENE, 21(4), 2000, pp. 805-810
Somatostatin (SRIF) is a potent antiproliferative signal for both normal an
d tumoral mammalian cells and an alteration in the SRIF receptor expression
pattern has been associated with carcinogenesis. In the present study, the
relevance of SRIF signaling to human male germ cell tumors was assessed at
the receptor level. The expression of five SRIF receptor (sst1-sst5) mRNAs
was estimated by RT-PCR and compared between normal and tumoral testes. Al
l 12 normal testicular tissues studied contained sst3 and sst5 receptor tra
nscripts whereas sst4 was present in almost all (11 of 12), sst1 transcript
s mere consistently absent while the majority (11/12) of normal samples stu
died did not contain sst2 mRNA, Parallel assessment of SRIF receptor mRNAs
in 10 seminoma testicular germ cell tumors showed expression of a single re
ceptor type, sst5, in all samples analyzed. All seminoma samples were deple
ted in transcripts corresponding to sst1 and sst2 receptors while either ss
t3 or sst4 mRNAs were absent in almost all (9 of 10) tumoral samples studie
d, The comparison of SRIF receptor expression between normal tissue and sem
inoma tumors thus points to a selective loss of sst3 and sst4 mRNA expressi
on in seminomas, Altogether these data indicate that: (i) normal human test
es are putative SRIF targets; (ii) loss of sst3 and sst4 SRIF receptor expr
ession might be associated with seminoma carcinogenesis.