Malignant melanoma is a neuroendocrine tumor that contains somatostatin rec
eptors (SSTRs), Adjuvant therapy for melanoma is limited. Because melanomas
arise from neural crest cells, we sought to evaluate the distribution of S
STR subtypes found in these tumors and their functional significance by ima
ging with In-111-pentetreotide scintigraph (OctreoScan). Octreotide binds w
ith greatest affinity to SSTR? and SSTR5. Studying the expression of SSTRs
in melanoma may demonstrate a potential role for octreotide in the treatmen
t of melanoma, A series of 23 melanomas from 17 patients who underwent rese
ction of regional or distant metastases were evaluated for the presence of
SSTRs by the reverse transcriptase-polymerase chain reaction (RT-PCR) using
primers specific for SSTR1 through SSTR5, Identity of RT-PCR products was
confirmed by Southern blot analysis, Sixteen patients underwent preoperativ
e OctreoScan, SSTR1 aas expressed in 96% of tumors, SSTR2 in 83%, SSTR3 in
61%, SSTR4 in 57%, and SSTR5 in 9%. OctreoScan imaged 63% of tumors, There
was no correlation between SSTR subtype expression and OctreoScan result. M
ost of the melanomas expressed mRNA for SSTR1 and SSTR2, with approximately
half expressing SSTR3 and SSTR4. The SSTR mRNA for SSTR2 appears to be tra
nscribed into functional protein that binds In-111-pentetreotide in more th
an half of these patients. Although OctreoScan has limited sensitivity for
localizing melanomas, tumors that can be imaged by OctreoScan mar be amenab
le to adjuvant therapy with octreotide or targeted therapy with high-energy
radioisotope-labeled octreotide, These studies clearly define melanoma as
a neuroendocrine turner, which may open new avenues for tumor control.