http://purl.uniprot.org/citations/28634667 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/28634667 | http://www.w3.org/2000/01/rdf-schema#comment | "BackgroundInterleukin (IL)-13 is an immunoregulatory, anti-inflammatory cytokine that is produced by numerous immune cells, and plasma membrane receptor for IL-13 (IL-13R) is known to be expressed in various human malignancies and in immune cells.MethodsThe authors evaluated the expression of IL-13R alpha 1 (IL-13Rα1, an IL-13R subtype) by immunohistochemistry in tissue microarrays of 1213 invasive breast cancer (IBC) samples to determine the prognostic value of IL-13Rα1 expression.ResultsHigh IL-13Rα1 expression was observed in 619 (51%) cases and was found to be associated with an older (≥50 years) age (p = 0.022), lymph node metastasis (p = 0.015), ductal and micropapillary histologic subtypes (p < 0.001), lymphovascular invasion (p = 0.012), HER2 positivity (p < 0.001), and a high (>20%) Ki-67 index (p = 0.039). No significant correlation was found between IL-13Rα1 expression and clinicopathological variables, including tumor size, histological grade, hormone receptor expressions, and tumor-infiltrating lymphocyte levels. Patients with high IL-13Rα1 expression showed poorer overall survival (p = 0.044) and disease-free survival (DFS, p = 0.001) than those with low/negative expression. Subgroup analysis revealed an association between IL-13Rα1 expression and survival for HER2-negative, but not for HER2-positive tumors. Multivariate analysis showed high IL-13Rα1 expression was an independent negative prognostic factor of DFS (p = 0.019).ConclusionsThe results of this study suggest the IL-13 and IL-13Rα1 interaction promotes cancer cell growth and metastasis, and IL-13Rα1 expression is a potential prognostic marker in IBC."xsd:string |
http://purl.uniprot.org/citations/28634667 | http://purl.org/dc/terms/identifier | "doi:10.1245/s10434-017-5907-2"xsd:string |
http://purl.uniprot.org/citations/28634667 | http://purl.uniprot.org/core/author | "Lee S.J."xsd:string |
http://purl.uniprot.org/citations/28634667 | http://purl.uniprot.org/core/author | "Lee B."xsd:string |
http://purl.uniprot.org/citations/28634667 | http://purl.uniprot.org/core/author | "Park M.H."xsd:string |
http://purl.uniprot.org/citations/28634667 | http://purl.uniprot.org/core/author | "Kim J.R."xsd:string |
http://purl.uniprot.org/citations/28634667 | http://purl.uniprot.org/core/author | "Kwon H.J."xsd:string |
http://purl.uniprot.org/citations/28634667 | http://purl.uniprot.org/core/author | "Bae Y.K."xsd:string |
http://purl.uniprot.org/citations/28634667 | http://purl.uniprot.org/core/date | "2017"xsd:gYear |
http://purl.uniprot.org/citations/28634667 | http://purl.uniprot.org/core/name | "Ann Surg Oncol"xsd:string |
http://purl.uniprot.org/citations/28634667 | http://purl.uniprot.org/core/pages | "3780-3787"xsd:string |
http://purl.uniprot.org/citations/28634667 | http://purl.uniprot.org/core/title | "Elevated Interleukin-13 Receptor Alpha 1 Expression in Tumor Cells Is Associated with Poor Prognosis in Patients with Invasive Breast Cancer."xsd:string |
http://purl.uniprot.org/citations/28634667 | http://purl.uniprot.org/core/volume | "24"xsd:string |
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