Expression and structure of interleukin 4 receptor (IL-4R) complex in human invasive pituitary adenomas

Lukui Chen, Yunsheng Liu, Yonghong Hou, Yoko Kato, Hirotoshi Sano, Tetsuo Kanno

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

Pituitary adenomas are frequently invasive of surrounding tissues, which adversely affects the surgical outcome and the disease-free survival of patients. In the present study, Interleukin 4 receptor (IL-4R) complex has been investigated to figure out whether the three subunits are overexpressed in human invasive pituitary adenomas. Reverse transcription-polymerase chain reaction (RT-PCR) analysis for interleukin 4 receptor α (IL-4Rα), interleukin 13 receptor α1 (IL-13Rα1), interleukin 2 receptor γc (IL-2Rγc) were performed on total RNA extracted from 10 non-invasive pituitary adenomas, 30 invasive pituitary adenomas, one glioblastoma multiforme, one normal human pituitary tissue sample and one normal human brain tissue sample. Quantitative real-time PCR and in situ immunofluorescence assay were performed in five invasive functioning pituitary adenoma samples and five invasive nonfunctioning pituitary adenoma samples. RT-PCR analysis for IL-4Rα, IL-13Rα1 and IL-2Rγc chains were overexpressed in invasive pituitary adenomas. The transcripts for three subunits were not/weakly expressed in normal pituitary tissue and normal brain tissue. The quantitative real-time PCR and in situ immunofluorescence assay confirmed the results of the RT-PCR analysis. Our results indicate that human invasive pituitary adenomas express type III IL-4R complex. These receptors may serve as a novel target for immunotoxin therapy in patients with invasive pituitary adenomas who are not amenable to total surgical resection or for recurrent cases.

Original languageEnglish
Pages (from-to)30-35
Number of pages6
JournalNeuroscience Letters
Volume417
Issue number1
DOIs
Publication statusPublished - 24-04-2007

All Science Journal Classification (ASJC) codes

  • Neuroscience(all)

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