The neuroendocrine nature of a subset of Leydig cells has already been
established. The present investigation deals with neuroendocrine char
acteristics of Leydig tumour cells. A number of neuroendocrine and neu
ronal markers were demonstrated in Leydig cell tumours of 7 men aged 2
5-41 years. The following substances were immunocytochemically tested
in Leydig tumour cells: the mo no amine-syn the sizing enzymes tyrosin
e hydroxylase and aromatic L-amino acid decarboxylase, the indoleamine
serotonin, the calcium-binding protein parvalbumin, the microtubule a
ssociated protein-2, neurofilament protein 200, synaptophysin, neuron
specific enolase, substance P and neuronal nitric oxide synthase (NOS)
. Compared to the normal interstitial cells beyond the tumours, all ne
oplastic cells showed a significantly weaker immunoreactivity for nerv
e cell markers as well as for testosterone and cyclic guanosine monoph
osphate (cGMP), which is usually accumulated by nitric oxide (NO). Thi
s provides evidence for a certain dedifferentiation of Leydig tumour c
ells. However, these results suggest that tumourous development of Ley
dig cells does not include loss of neuronal phenotype. Moreover, on th
e assumption that 'neuronal' Leydig cells exist beside 'non-neuronal'
ones in normal testicular tissue, we propose the hypothesis that 'neur
onal' Leydig cells can transform to tumour cells.