Comprehensive analysis of PTEN status in Sezary syndrome.

Cristina Cristofoletti, Maria Cristina Picchio, Cristina Lazzeri, Valeria Tocco, Elena Pagani, Antonella Bresin, Barbara Mancini, Francesca Passarelli, Antonio Facchiano, Enrico Scala, Giuseppe Alfonso Lombardo, Maria Cantonetti, Elisabetta Caprini, Giandomenico Russo, Maria Grazia Narducci

Research output: Contribution to journalArticlepeer-review


Sézary syndrome (SS) is an incurable leukemic variant of cutaneous T-cell lymphoma characterized by recurrent chromosomal alterations, among which, chromosome 10q deletion is very frequent. In this study, we investigated the PTEN status, on locus 10q23, in 44 SS patients; our findings show that PTEN is deleted in 36% of SS cases, whereas PTEN downregulation is observed in almost all of the samples evaluated by quantitative reverse-transcriptase polymerase chain reaction and Western blotting analysis. Neither DNA sequence mutation nor promoter hypermethylation were found at the PTEN locus, but we demonstrate that PTEN level can be also reduced by a group of miRs previously found upregulated and of prognostic relevance in SS; particularly, miR-21, miR-106b, and miR-486 were able to control PTEN abundance either in vitro or in vivo. Finally, because reduced PTEN activates the PI3/AKT-mediated pathway of cell growth and survival, we demonstrate that PTEN deficiency is associated with activated AKT in skin resident but not circulating SS cells, suggesting that the cutaneous milieu may strongly contribute to the SS cell growth. To our knowledge, this is the first study fully exploring the PTEN status in a large cohort of SS patients, unveiling potential elements of clinical utility in this malignancy.

Original languageEnglish
Pages (from-to)3511-3520
Number of pages10
Issue number20
Publication statusPublished - Nov 14 2013

ASJC Scopus subject areas

  • Hematology
  • Biochemistry
  • Cell Biology
  • Immunology
  • Medicine(all)


Dive into the research topics of 'Comprehensive analysis of PTEN status in Sezary syndrome.'. Together they form a unique fingerprint.

Cite this