Point mutation at single tyrosine residue of novel oncogene NOK abrogates tumorigenesis in nude mice

Yue Chen, Ying Hua Li, Xi Ping Chen, Li Min Gong, Shu Ping Zhang, Zhi Jie Chang, Xiu Fang Zhang, Xin Yuan Fu, Li Liu

Research output: Contribution to journalArticle

27 Scopus citations

Abstract

Receptor protein-tyrosine kinases (RPTKs) are tightly regulated during normal cellular processes including cell growth, differentiation, and metabolism. Recently, a RPTK-like molecule named novel oncogene with kinase-domain (NOK) has been cloned and characterized. Overexpression of NOK caused severe cellular transformation as well as tumorigenesis and metastasis in nude mice. In the current study, we generated two tyrosine→phenylalanine (Y→F) point mutations (Y327F and Y356F) within the endodomain of NOK that are well conserved in many RPTK subfamilies and are the potential tyrosine phosphorylation sites important for major intracellular signaling. Using BaF3 cells stably expressing the ectodomain of mouse erythropoietin receptor, and the transmembrane and endodomain of NOK (BaF3-E/N), we were able to show that point mutations at either Y327 or Y356 dramatically blocked cellular transformation by NOK as examined by colony formation and cellular DNA synthesis. In addition, tumorigenesis induced by BaF3-E/N was completely abrogated upon the introduction of either single mutation. Importantly, signaling studies revealed that the activation of extracellular signal-regulated kinase was inhibited by Y356F and was significantly reduced by Y327F. Both mutations significantly impaired Akt phosphorylation. Interestingly, both mutations did not affect the kinase activity of NOK. Moreover, apoptotic analysis revealed that both mutations accelerated cell death by activating caspase-3-mediated pathways. Thus, our study shows that these potential tyrosine phosphorylation sites may play critical roles in NOK-mediated tumorigenesis both in vitro and in vivo.

Original languageEnglish (US)
Pages (from-to)10838-10846
Number of pages9
JournalCancer Research
Volume65
Issue number23
DOIs
StatePublished - Dec 1 2005

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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    Chen, Y., Li, Y. H., Chen, X. P., Gong, L. M., Zhang, S. P., Chang, Z. J., Zhang, X. F., Fu, X. Y., & Liu, L. (2005). Point mutation at single tyrosine residue of novel oncogene NOK abrogates tumorigenesis in nude mice. Cancer Research, 65(23), 10838-10846. https://doi.org/10.1158/0008-5472.CAN-05-1091