HACE1 Is a Tumor Suppressor Gene Candidate in Natural Killer Cell Neoplasms


Kuecuek C., Hu X., Iqbal J., Gaulard P., Klinkebiel D., Cornish A., ...More

AMERICAN JOURNAL OF PATHOLOGY, vol.182, no.1, pp.49-55, 2013 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 182 Issue: 1
  • Publication Date: 2013
  • Doi Number: 10.1016/j.ajpath.2012.09.012
  • Journal Name: AMERICAN JOURNAL OF PATHOLOGY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.49-55
  • Dokuz Eylül University Affiliated: No

Abstract

HACE1 is an E3 ubiquitin ligase located in 6q21, the genomic region frequently deleted in natural killer (NK) cell malignancies. Here, we report HACE1 as a candidate tumor suppressor gene silenced through a combination of deletion and cytosine phosphate guanine island hypermethylation. We detected deletion of HACE1 in malignant NK cell lines (6 of 9, 67%) and primary biopsies (5 of 15, 33%) by quantitative PCR, with most of the specimen showing cytosine phosphate guanine island hypermethylation in the remaining allele, Leading to Low mRNA transcription. The ectopic expression of HACE1 in an HACE1-null NK cell Line led to apoptosis and G(2)/M cell cycle arrest. Moreover, HACE1 expression was up-regulated in IL-2-activated normal NK cells and NK cells cocultured with an engineered NK cell target, K562 Clone 9.mbIL21, suggesting its rote in the regulation of NK cell homeostasis. In conclusion, HACE1 is another potent tumor suppressor gene located within the 6q21 region, and loss of function of multiple tumor suppressor genes within 6q21 may be a critical determinant of NK cell Lymphomagenesis. (Am J Pathol 2013, 182: 49-55; http://dx.doi.org/10.1016/j.ajpath.2012.09.012)