key: cord-0002022-765ufb5i
authors: SAKAI, Kosei; YONEZAWA, Tomohiro; YAMAWAKI, Hideyuki; OYAMADA, Toshifumi
title: Alteration of somatostatin receptor 2 expression in canine mammary gland tumor
date: 2015-05-18
journal: J Vet Med Sci
DOI: 10.1292/jvms.15-0002
sha: 75fbdec55c05102f8337e48dda0c8b6cf27dac52
doc_id: 2022
cord_uid: 765ufb5i

Somatostatin receptor 2 (SSTR2) is a negative regulator of cell proliferation in human breast cancer. Since there is little information about SSTR2 in canine mammary gland tumor (MGT), we clarified its distribution and expression level in normal mammary gland, benign MGT and malignant MGT. SSTR2 expression determined by immunohistochemical staining was observed in the cytoplasm of luminal epithelial cells. The intensity was negatively correlated with malignancy: normal tissues and some of the benign tumors had the highest levels, while the malignant tumors had little or no SSTR2 expression. As for the Western blotting, SSTR2 protein level in benign tumors was significantly lower than the normal mammary gland. On the other hand, SSTR2 protein levels in two of three malignant tumors were higher than the other groups. These results suggest that SSTR2 expression alters according to the malignancy of canine MGT.

Somatostatin (SST) is a peptide hormone produced in the hypothalamus, pancreas and intestine; it regulates both endocrine and exocrine gland function [17] , and downregulates cell proliferation in various tissues of many species including dogs [1, 3, 4, 10, 14] . Among the SST receptor (SSTR) superfamily, SSTR2 is the most dominant receptor, with the highest affinity to the ligand and the strongest antiproliferative effect [3] . In human breast cancer, tumor tissues that express SSTRs are less aggressive and more differentiated than tumors with little SSTRs expression, which are massive and highly malignant [5] . These findings lead to the speculation that SSTR signal transduction is closely related to the malignancy of human breast cancer.

In dogs, all subtypes of SSTRs, except SSTR4, have been already identified, and their expression was confirmed in just several tissues, such as pituitary and pancreas [2, 16] . Although SSTRs are predicted to be a molecular target of breast cancer therapy, there is little information about SSTRs in dogs. Hence, in this study, we examined and compared the distribution and expression of SSTR2 in normal canine mammary tissues, benign mammary gland tumor (MGT) and malignant MGT. Immunohistochemistry and Western blotting methods were utilized.

All experiments were approved by the Committees on the Ethics of Animal Experiments of Kitasato University and the University of Tokyo. For immunohistochemistry, 48 samples of canine mammary gland tissue embedded in paraffin blocks were obtained from the histopathological files in the Veterinary Pathology Laboratory, Kitasato University. Although the classification method about simple carcinoma is under controversy [18] , the diagnosis of all specimens was based on the WHO classification [11] . Immunohistochemical staining was performed using the rabbit polyclonal antibodies against human SSTR2 (1:300 dilution, bs-1138R, Bioss, Boston, MA, U.S.A.). Peroxidase-conjugated anti-rabbit immunoglobulin G (Histofine Simple Stain MAX-PO (R), Nichirei, Tokyo, Japan) was used as the secondary antibody. After immunoreaction, sections were colorized with diaminobenzidine and counterstained with hematoxylin. Canine pancreas tissues were used as positive controls. Negative controls were carried out by replacing the primary antibodies with antibody diluents.

For Western blotting, 12 canine mammary gland tissues (4 normal, 4 simple adenomas, one complex adenoma and 3 simple carcinomas), harvested and flash frozen in liquid nitrogen, were obtained either from experimental animals or from patients undergoing surgery for mammary gland tumors at the Kitasato University Veterinary Teaching Hospital. We performed Western blotting analysis according to a previously reported protocol [12] . Twelve micrograms of protein were loaded in each well. The human SSTR2 antibody used in immunohistochemistry analysis (1:300 dilution) was also used in Western blotting. Samples were visualized using horseradish peroxidase-conjugated secondary antibodies and the EZ-ECL system (Biological Industries, Kibbutz Beit Hesmek, Israel). The expression level of SSTR2 in each sample was normalized to total actin (1:500 dilution, MAB1501, Sigma-Aldrich, St. Louis, MO, U.S.A.) expression on the same membrane as an internal control.

A summary of immunohistochemical data is shown in Fig.  1 was restricted to the luminal epithelial cells, although myoepithelial and stromal cells were present in the specimens. The samples are grouped into three groups in Table 1 based on their diagnoses. The first group contains tissues from normal or hyperplastic mammary glands. SSTR2 immunoreactivity in this group was readily observed in the cytoplasm of the luminal epithelial cells. The second group of tissues was from animals diagnosed with benign tumors. These were simple or complex mammary adenoma or mixed tumors. SSTR2

expression in approximately half of the tissues of this group was similar to the first group, with a similar immunoreactive pattern that was detected in the luminal epithelial cells; the other half of this group had little to no immunoreactivity. Samples from the third group were from animals diagnosed with malignant tumors: simple or complex mammary carcinoma or malignant mixed tumors. These tissues had negative or weakly positive immunoreactivity.

To evaluate the quantitative expression levels of SSTR2, we performed Western blotting (Fig. 2) . In Western blotting, a specific band corresponding to approximately 50-kDa molecular weight was detected. In the benign MGT, the SSTR2 protein level was lower than in normal tissues. The levels of SSTR2 protein in two of three malignant MGTs were higher than in the other groups, while the level in one of three was around normal. In these malignant samples, there were also no clear signals of SSTR2 in immunohistochemistry (see the Supplementary Fig. 1) , which is coincident with the immunohistochemical results in our other samples (Fig. 1) . Further, there was no difference among tissue types: simple, complex and mixed tumors (data not shown).

SSTR2 is expressed in the luminal epithelial cells of the mammary tissues and breast cancers in humans [8] . In our study, SSTR2 expression in canine tumors was also limited to the luminal epithelial cells, specifically to the cytoplasm. SSTR expression in humans has also been reported to be (2) 1 (50%) 1 (50%) 0 (0%) Simple adenoma (12) 2 (16.7%) 5 (41.7%) 5 (41.7%) Complex adenoma (7) 1 (14.3%) 2 (28.6%) 4 (57.1%) Benign mixed tumor (5) 1 (20%) 2 (40%) 2 (40%) Simple carcinoma (10) 0 (0%) 5 (50%) 5 (50%) Complex carcinoma (5) 0 (0%) 3 (60%) 2 (40%) Malignant mixed tumor (2) 0 (0%) 1 (50%) 1 (50%) +: Strongly positive; ±: Weakly positive; −: Negative.

down-regulated in more aggressive and less differentiated benign breast tumors [5] . The results of immunohistological staining agree with these human studies [5, 8] . Protein levels of the benign tumors were also less than the normal or hyperplastic tissue, as shown by Western blotting. These findings suggest that SSTR2 deficiency in canines may contribute to the development of benign tumors. Alteration of SSTR2 expression in the MGT is not fully understood. Some studies in human breast cancer report that the SSTR2 immunohistochemical reaction was less in malignant tumors than in normal tissue, but others report the opposite relationship for SSTR2 mRNA. For instance, Reubi et al. detected SSTR2-positive immunoreactivity in only 3/39 (8%) of human malignant breast tumors [15] , while Orlando et al. performed q-PCR of 169 human breast cancers and concluded that the SSTR2 mRNA level was tremendously higher in human breast cancers than in unaffected tissues [13] . Evans et al. found SSTR2 mRNA expression in almost all breast carcinoma, but in only approximately half of benign tumors or normal breast tissues [7] . In the present study, all of SSTR2 immunohistochemical intensity in malignant tumors was lower or negative compared to normal tissues, whereas SSTR2 protein levels in two of three malignant tumors were higher than the other groups in the Western blotting analysis. Although mRNA levels were not determined in these specimens, our standings tended to be compatible with the previous results and this is the first report presenting the paradoxical results within one study.

We had conflicting results between immunohistochemical reactivity and protein level of SSTR2 in malignant tumors. In this study, the same primary antibody to SSTR2 was used for both immunohistochemistry and Western blotting. However, very little reactivity was observed in immunohistochemistry, while Western blotting detected a large amount of protein. Indeed, it is not so rare that there is some discrepancy between the results of immunohistochemistry and Western blotting [6, 9] . Although further studies are needed to understand the reasons for these results, there are several hypotheses that could account for them. 1) In immunohistochemistry, the tissue is fixed in 10% neutral buffered formalin, and the epitope may be obscured or cross-linked due to experimental conditions. 2) Because Western blotting was performed after the reduction treatment, a conformational change in the protein may alter the intensity of immunoreactivity.

In conclusion, we examined the distribution and expression of SSTR2 in canine mammary gland tissues. SSTR2 was mainly observed in the cytoplasm of luminal epithelial cells. There was less expression of SSTR2 in benign MGTs than in normal tissues. In malignant MGT, immunohistochemical intensity of SSTR2 was low, although SSTR2 protein levels were high. It is suggested that SSTR2 expression changes with malignancy of canine MGT. 

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