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• W2617355237 endingPage "89969" @default.
• W2617355237 startingPage "89958" @default.
• W2617355237 abstract "Paragangliomas are predominantly benign tumors, but in some cases invasive growth and also metastasis are observed. Given the limited number of nonsurgical treatment options, novel target structures for diagnostics and therapy of this tumor entity are urgently needed. In the present study, expression of all five somatostatin receptor (SST) subtypes, chemokine receptor CXCR4 and endothelin receptor type A (ETA) was assessed by means of immunohistochemistry in a total of 66 paraffin-embedded paraganglioma samples from 55 patients. The stainings were rated by means of the Immunoreactive Score and correlated to clinical data and to succinate dehydrogenase subunit B (SDHB) expression. SST2A was by far the most prominent receptor in the paragangliomas investigated. It was present in 89% of the tumors at a high intensity, followed by SST5, SST3, SST1 and SST4, which were detected in 47%, 35%, 35% and 13% of the samples, respectively. SDHB positive tumors exhibited significantly higher SST2A and SST3 expression as compared to SDHB negative cases. There was no correlation between SST and Ki-67 expression or grading of the tumors and no difference in SST expression between primary tumors and metastases. Cell surface expression of CXCR4 and ETA was detected only in few samples. On tumor capillaries, however, exceptionally strong staining for these two receptors was noticed in the vast majority of the tumors. In conclusion, paragangliomas are well suited for SST2A-based diagnostics and treatment modalities. An indirect targeting of these highly vascularized tumors via CXCR4 or ETA may also represent a promising future strategy." @default.
• W2617355237 created "2017-06-05" @default.
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• W2617355237 date "2017-09-23" @default.
• W2617355237 modified "2023-10-18" @default.
• W2617355237 title "Evaluation of somatostatin, CXCR4 chemokine and endothelin A receptor expression in a large set of paragangliomas" @default.
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• W2617355237 doi "https://doi.org/10.18632/oncotarget.21194" @default.
• W2617355237 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5685723" @default.
• W2617355237 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29163802" @default.
• W2617355237 hasPublicationYear "2017" @default.
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