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Published on: February 21, 2014
Somatostatin receptor SSTR2A and SSTR5 expression in neuroendocrine breast cancer
Robert Terlević1, Melita Perić Balja2, Davor Tomas3
1Pula General Hospital, Zagrebacka 30, 52100 Pula, Croatia; "Ljudevit Jurak" Department of Pathology and Cytology, Clinical Hospital Center "Sestre milosrdnice", Vinogradska cesta 29, 10000 Zagreb, Croatia.
Abstract:
Neuroendocrine breast cancer (NEBC) is a group of rare tumors, which could benefit from therapy targeting the somatostatin receptors (SSTRs). In particular, SSTR2A and SSTR5 are potential targets given their consistent expression in gastrointestinal and pancreatic primary and metastatic neuroendocrine cancers. Currently, there are no studies describing the expression of SSTRs in NEBC. The purpose of our study was to characterize the immunohistochemical expression of SSTR2A and SSTR5 in a cohort of NEBC. Thirty-one primary NEBC cases were analyzed, and SSTR2A and SSTR5 immunohistochemistry performed and scored using the modified immunoreactive score proposed by Remmele and Stanger. All patients were females with a mean age of 66.6 years (SD = 14). 77% of cases were histological grade 2. SSTR2A showed a weak positivity in 11 cases (35.5%), moderate positivity in 6 cases (19.4%) and strong positivity in 5 cases (16.1%). Nine cases were negative for SSTR2A (29%). SSTR5 showed a weak positivity in 16 cases (51.6%), moderate positivity in 6 cases (19.4%), while no cases showed strong positivity. Nine cases were negative for SSTR5 (29%). Five cases were negative for both SSTR2A and SSTR5. A weak to moderate SSTR2A and SSTR5 expression was observed in 50-70% of the cases. A subset of NEBCs with strong SSR2A expression may benefit from SSTRs targeted therapy. These results need further validation in a larger series including metastatic NEBC, to provide potential therapeutic targets for patients with advanced disease.
Insights
Neuroendocrine breast cancer (NEBC) shows somatostatin receptor (SSTR) expression, with SSTR2A and SSTR5 present in over half of cases. Some NEBC patients may benefit from SSTR-targeted therapies.
Area of Science:
- Oncology
- Endocrinology
- Pathology
Background:
- Neuroendocrine breast cancer (NEBC) is rare, and therapies targeting somatostatin receptors (SSTRs) are promising.
- SSTR2A and SSTR5 are known targets in other neuroendocrine tumors but their expression in NEBC is uncharacterized.
Purpose of the Study:
- To investigate the immunohistochemical expression of SSTR2A and SSTR5 in primary NEBC.
- To determine the potential of SSTR-targeted therapies for NEBC.
Main Methods:
- Analysis of 31 primary NEBC cases using immunohistochemistry for SSTR2A and SSTR5.
- Scoring of receptor expression using the modified immunoreactive score.
Main Results:
- SSTR2A was expressed (weak, moderate, or strong) in 71% of NEBC cases.
- SSTR5 was expressed (weak or moderate) in 71% of NEBC cases.
- Five cases (16.1%) showed no expression of either SSTR2A or SSTR5.
Conclusions:
- A significant proportion of NEBC cases express SSTR2A and SSTR5, suggesting potential therapeutic utility.
- Further validation in larger, metastatic NEBC cohorts is needed to confirm SSTR-targeted therapy benefits.
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