| Literature DB >> 29205518 |
David Lemchak1, Swati Banerjee1, Shaunak S Digambar1, Brian L Hood2, Thomas P Conrads2, Jaroslaw Jedrych1, Larisa Geskin1,3, Oleg E Akilov1.
Abstract
While mycosis fungoides (MF) is typically an indolent malignancy, it may infrequently undertake an aggressive course. We used proteomic analyses to identify a biomarker of the aggressive course of MF. Results of this investigation demonstrated that PARP-1, heat-shock protein family A (Hsp70) member 1 like (HSAP1L), Hsp70 member 1A (HSPA1A), ATP-depending RNA helicase (DDX17) and the α-isoform of lamina-associated polypeptide 2 (TMPO) had higher expression in aggressive disease versus non-aggressive. Moreover, PARP-1 was overexpressed in patients with early stage of MF who developed later an aggressive disease. PARP-1 was evaluated as a new target for therapy, demonstrating the selective dose-dependent cytotoxic effect of PARP inhibitors on Sézary cells in comparison with non-malignant lymphocytes. In conclusion, we believe that PARP-1 may serve not only as a biomarker at initial biopsies for a disease that may become aggressive but also as a new therapeutic target of advanced MF and Sézary syndrome.Entities:
Keywords: PARP-1; Sezary syndrome; biomarkers; cutaneous lymphoma; mycosis fungoides
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Year: 2017 PMID: 29205518 PMCID: PMC5790623 DOI: 10.1111/exd.13477
Source DB: PubMed Journal: Exp Dermatol ISSN: 0906-6705 Impact factor: 3.960