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The potential of somatostatin receptor 2 as a novel therapeutic target in salivary gland malignant tumors

  • Original Article – Cancer Research
  • Published:
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Abstract

Background

Treatment regimens for patients with metastatic or recurrent post-radiation, locoregional, unresectable salivary cancer are limited. An inverse correlation between somatostatin receptor 2 (SSTR2) and the proliferating marker Ki-67 in neuroendocrine tumors has enabled a treatment plan for metastatic disease, utilizing peptide receptor radionuclide therapy. Interestingly, healthy salivary glands express high levels of SSTR2. In this study, the presence of SSTR2, its correlation with Ki-67 in glandular salivary carcinomas and the clinical applicability thereof was determined.

Methods

In the retrospective part of this study, 76 adequate tumor tissue specimens obtained from patients diagnosed with primary or metastatic salivary carcinomas between 1988 and 2016, were collected for tissue array and histologically classified. Immunohistochemistry was performed to determine the presence, relative expression and potential correlation of SSTR2 and Ki-67. The clinical significance of SSTR2 expression was determined by prospectively assessing 68Ga-DOTATATE uptake using PET-CT imaging, in patients diagnosed with metastatic salivary gland malignant tumors between 2015 and 2016.

Results

Sixty-three primary cancer tumors and 14 metastatic tumors were tested. All tumor subtypes were found to express SSTR2 to some extent. The highest expression was seen in Mucoepidermoid carcinoma (MEC) tissues where the majority of specimens (86.4%) expressed SSTR2. A relatively strong immunohistochemical staining score for SSTR2 was observed in MEC, adenoid cystic carcinoma and polymorphous adenocarcinoma. Interestingly, an inverse correlation between SSTR2 and Ki-67 expressions was observed (44%) in MEC tissue. Uptake of 68Ga-DOTATATE was visualized using PET-CT imaging in 40% of patients, across metastatic MEC and ACC. All observations were found to be statistically significant.

Conclusion

This study confirms the expression of SSTR2 in glandular salivary carcinomas and an inverse correlation in expression levels between SSTR2 and Ki-67. This lays a foundation for novel treatment options in salivary metastatic cancers where SSTR2 may be a potential novel therapeutic target.

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Availability of data and material

The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.

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Funding

This study has not been externally funded.

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Authors and Affiliations

Authors

Contributions

Amichay Meirovitz: study design, conduction, data analysis and manuscript preparation. Karny Shouchane-Blum: pathological and histological analysis and manuscript preparation. Alexander Maly: pathological and histological analysis. Evgeniya Bersudski: sample collection. Nir Hirshoren: sample collection. Ross Abrams: data analysis and manuscript preparation. Aron Popovtzer: data analysis and manuscript preparation. Marina Orevi: nuclear medicine analysis. Jeffrey Weinberger: study design and manuscript preparation.

Corresponding author

Correspondence to Amichay Meirovitz.

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None of the authors have any conflicts of interest to declare.

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Declaration of Helsinki approval: approval no. 0421-15-HMO.

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Informed consent was obtained from all individual participants included in the study.

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Only non-identifying participant data will be published.

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Meirovitz, A., Shouchane-Blum, K., Maly, A. et al. The potential of somatostatin receptor 2 as a novel therapeutic target in salivary gland malignant tumors. J Cancer Res Clin Oncol 147, 1335–1340 (2021). https://doi.org/10.1007/s00432-021-03538-1

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  • DOI: https://doi.org/10.1007/s00432-021-03538-1

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