NLRR1 enhances EGF-mediated MYCN induction in neuroblastoma and accelerates tumor growth in vivo

Shamim Hossain, Atsushi Takatori, Yohko Nakamura, Yusuke Suenaga, Takehiko Kamijo, Akira Nakagawara

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

Neuronal leucine-rich repeat protein-1 (NLRR1), a type-1 transmembrane protein highly expressed in unfavorable neuroblastoma, is a target gene of MYCNthat is predominately expressed in primary neuroblastomas with MYCN amplification. However, the precise biolog ical role of NLRR1 in cell proliferation and tumor progression remains unknown. To investigate its functional importance, we examined the role of NLRR1 in EGF and insulin growth factor-1 (IGF-1)-mediated cell viability. We found that NLRR1 positively regulated cell proliferation through activation of extracellular signal-regulated kinase mediated by EGF and IGF-1. Interestingly, EGF stimulation induced endogenous MYCN expression through Sp1 recruitment to the MYCN promoter region, which was accelerated in NLRR1-expressing cells. The Sp1-binding site was identified on the promoter region for MYCN induction, and phosphorylation of Sp1 was important for EGF-mediated MYCN regulation. In vivo studies confirmed the proliferation-promoting activity of NLRR1 and established an association between NLRR1 expression and poor prognosis in neuroblastoma. Together, our findings indicate that NLRR1 plays an important role in the development of neuroblastoma and therefore may represent an attractive therapeutic target for cancer treatment.

Original languageEnglish
Pages (from-to)4587-4596
Number of pages10
JournalCancer Research
Volume72
Issue number17
DOIs
Publication statusPublished - Sep 1 2012
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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