S. Schulz et al., IMMUNOCYTOCHEMICAL DETECTION OF SOMATOSTATIN RECEPTORS SST(1), SST(2A), SST(2B), AND SST(3) IN PARAFFIN-EMBEDDED BREAST-CANCER TISSUE USINGSUBTYPE-SPECIFIC ANTIBODIES, Clinical cancer research, 4(9), 1998, pp. 2047-2052
The long-acting somatostatin analogue octreotide (SMS 201-995) inhibit
s growth of certain breast cancer cell lines ipl vivo and in vitro. Be
cause the antiproliferative action of octreotide depends on at Least t
he presence of somatostatin receptors, it is crucial to determine the
pattern of somatostatin receptor protein expression on the tumor cells
, In the present study, we have raised polyclonal antibodies to somato
statin receptor subtypes (ssts) sst(1), sst(2A), sst(2B), and sst(3) u
sing peptides corresponding to their COOH-terminal sequences. These an
tisera were used for immunocytochemical staining of paraffin sections
of 33 primary breast cancers. Somatostatin receptor-like immunoreactiv
ity (Li) was predominantly localized to the plasma membrane of the tum
or cells, In the vest majority of positively stained tumors, somatosta
tin receptor-ii was uniformly present on nearly all tumor cells, Both
the level and the pattern of expression of ssts varied greatly between
individual carcinomas. sst(2A)-li and/or sst(2B)-Li was detectable in
28 tumors (85%); among these, 14 tumors (42%) showed particularly hig
h levels of sst(2)-Li, sst(1)-Li was found in 17 (52%) cases and sst(3
)-Li in 16 (48%) cases. The expression of ssts was independent of pati
ent age, menopausal status, diagnosis, histological grade, and levels
of estrogen and progesterone receptors, The immunocytochemical determi
nation of somatostatin receptor status allows direct detection of rece
ptor protein on the tumor cells and, hence, may provide more precise i
nformation than reverse transcription-PCR for predicting response to o
ctreotide therapy in breast cancer.