Constitutive degradation of PML/RARα through the proteasome pathway mediates retinoic acid resistance

Mirco Fanelli, Saverio Minucci, Vania Gelmetti, Clara Nervi, Carlo Gambacorti-Passerini, Pier Giuseppe Pelicci

Research output: Contribution to journalArticlepeer-review

Abstract

PML/RARα is the leukemogenetic protein of acute promyelocytic leukemia (APL). Treatment with retinoic acid (RA) induces degradation of PML/RARα, differentiation of leukaemic blasts, and disease remission. However, RA resistance arises during RA treatment of APL patients. To investigate the phenomenon of RA resistance in APL, we generated RA-resistant sublines from APL-derived NB4 cells. The NB4.007/6 RA-resistant subline does not express the PML/RARα protein, although its mRNA is detectable at levels comparable to those of the parental cell line. In vitro degradation assays showed that the half-life of PML/RARα is less than 30 minutes in NB4.007/6 and longer than 3 hours in NB4. Treatment of NB4.007/6 cells with the proteasome inhibitors LLnL and lactacystin partially restored PML/RARα protein expression and resulted in a partial release of the RA-resistant phenotype. Similarly, forced expression of PML/RARα, but not RARα, into the NB4/007.6 cells restored sensitivity to RA treatment to levels comparable to those of the NB4 cells. These results indicate that constitutive degradation of PML/RARα protein may lead to RA resistance and that PML/RARα expression is crucial to convey RA sensitivity to APL cells.

Original languageEnglish
Pages (from-to)1477-1481
Number of pages5
JournalBlood
Volume93
Issue number5
Publication statusPublished - Mar 1 1999

ASJC Scopus subject areas

  • Hematology

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