Abstract

Mycosis fungoides (MF) and its leukemic variant Sézary syndrome (SS) comprise the majority of CTCL, a heterogenous group of non-Hodgkins lymphomas involving the skin. The CTCL’s resistance to chemotherapy and the lack of full understanding of their pathogenesis request further investigation. With the view of a more targeted therapy, we evaluated in vitro the effectiveness of bortezomib and methotrexate, as well as their combination in CTCL cell lines, regarding apoptosis induction. Our data are of clinical value and indicate that the bortezomib/methotrexate combinational therapy has an inferior impact on the apoptosis of CTCL compared to monotherapy, with bortezomib presenting as the most efficient treatment option for SS and methotrexate for MF. Using PCR arrays technology, we also investigated the alterations in the expression profile of genes related to DNA repair pathways in CTCL cell lines after treatment with bortezomib or methotrexate. We found that both agents, but mostly bortezomib, significantly deregulate a large number of genes in SS and MF cell lines, suggesting another pathway through which these agents could induce apoptosis in CTCL. Finally, we show that SS and MF respond differently to treatment, verifying their distinct nature and further emphasizing the need for discrete treatment approaches.

Highlights

  • Cutaneous T-cell lymphomas (CTCLs) are rare skin malignancies, comprising a heterogeneous group of non-Hodgkin lymphomas derived from skin-homing mature T-cells [1]

  • The higher apoptotic effect was observed after treatment with bortezomib, followed by the two drugs’ combination (11.76% and 7.61% vs 1.53% respectively, p = 0.000) and methotrexate (3.98% vs 1.53%, p = 0.000) (Fig 1A and 1D)

  • Many chemotherapeutic agents have been used in the treatment of Mycosis fungoides (MF)/Sezary syndrome (SS), no single therapy has shown superior or efficient effect in the long term, especially for refractory, extensive and/or advanced disease, which are mostly approached through systemic treatments that fail to provide a permanent therapeutic solution [33]

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Summary

Introduction

Cutaneous T-cell lymphomas (CTCLs) are rare skin malignancies, comprising a heterogeneous group of non-Hodgkin lymphomas derived from skin-homing mature T-cells [1]. Mycosis fungoides (MF) and Sezary syndrome (SS) are considered as the commonest CTCL. Bortezomib and Methotrexate Interfere with the DNA Repair Mechanisms in Cutaneous T-Cell Lymphoma breast cancer stem cells: applications in prognosis, diagnosis & treatment’, MIS: 377177

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