Leptin, a hormone mainly secreted from adipose tissue, communicates a metabolic signal
to the adrenal gland. Ob-Receptor (Ob-R) expression was reported in rat, mice and
human adrenal glands. This study intended to investigate possible differences in the
Ob-R expression and distribution of Ob-R protein in human adrenal tumors as compared
to normal adrenal tissue. Proliferative effects of leptin were analyzed in the human
adrenocortical carcinoma cell line (NCI-H295). The full length Ob-R mRNA and the isoforms
B219.1 and B219.3 could be demonstrated by RT-PCR in all adrenal tumors (n = 8), the
tumor cell line (NCI-H295) and normal tissue. In contrast the Ob-R isoform B219.2
was absent in the carcinoma cell line and in most of the adrenal tumors (n = 5), whereas
it was present in normal adrenals. The Ob-R protein could be demonstrated in benign
and malignant adrenocortical tumors. Pheochromocytomas showed only a weak immunostaining
with the human Ob-R antibody. Human leptin did not affect the proliferation or variability
of adrenal tumor cells as demonstrated by [3H]-thymidine assay and WST-1 test. In conclusion, although functional leptin receptors
are expressed in human adrenal tumors, leptin does not regulate tumor cell proliferation.
Key words
Immunostaining - Leptin Receptor - Adrenal Pathologies