Abstract

Cutaneous T-cell lymphoma (CTCL) represents a heterogeneous group of potentially devastating primary skin malignancies. Despite decades of intense research efforts, the pathogenesis is still not fully understood. In the early stages, both clinical and histopathological diagnosis is often difficult due to the ability of CTCL to masquerade as benign skin inflammatory dermatoses. Due to a lack of reliable biomarkers, it is also difficult to predict which patients will respond to therapy or progress towards severe recalcitrant disease. In this review, we discuss recent discoveries concerning dysregulated microRNA (miR) expression and putative pathological roles of oncogenic and tumor suppressive miRs in CTCL. We also focus on the interplay between miRs, histone deacetylase inhibitors, and oncogenic signaling pathways in malignant T cells as well as the impact of miRs in shaping the inflammatory tumor microenvironment. We highlight the potential use of miRs as diagnostic and prognostic markers, as well as their potential as therapeutic targets. Finally, we propose that the combined use of miR-modulating compounds with epigenetic drugs may provide a novel avenue for boosting the clinical efficacy of existing anti-cancer therapies in CTCL.

Highlights

  • Etiology of of Cutaneous Cutaneous T T Cell Cell Lymphoma LymphomaCutaneous T-cell lymphoma lymphoma (CTCL) comprises a heterogeneous heterogeneous group of of non-Hodgkin non-Hodgkin lymphomas characterized by the proliferation of neoplastic T cells in a chronic chronic inflammatory inflammatory environment

  • The oncogenic activity of bromodomain-containing protein 4 (BRD4) was inhibited by restoring the miR-29b activity by bortezomib treatment or directly by a bromodomain inhibitor (JQ1), both interventions leading to the prevention of disease progression in CTCL [111]

  • Preclinical studies demonstrated that antagomiR-214 treatment significantly decreased disease severity in a CTCL mouse model, and miR-21 seems to be highly involved in promoting malignant growth [83]

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Summary

Etiology

Cutaneous T-cell lymphoma lymphoma (CTCL) comprises a heterogeneous heterogeneous group of of non-Hodgkin non-Hodgkin lymphomas characterized by the proliferation of neoplastic T cells in a chronic chronic inflammatory inflammatory environment. Despite diagnosisimpossible [1,2] It iswhich generally impossible predict which patients suffer an intense research efforts in recent years,intense the pathogenesis of CTCL still remains poorly understood. Despite research efforts in recent years, the pathogenesis of Genetic, epigenetic, and environmental factors have all been proposed to be implicated in [1,4,5]. Lines of NFκB evidence have pointed a key role for epigenetic dysregulation in the potentiateseveral constitutive signaling [8,9,10,11,12,13].towards This is a notion further byofthe efficacy of therapeutic drugs towards a keyofrole for [14,15,16]. Stages of mycosis fungoides (MF). (D) A patient suffering from Sézary syndrome (SS)

MicroRNAs in Health and Disease
Dysregulation of miRs in CTCL
OncomiRs in CTCL Pathogenesis
Role of miR-155 in Disease Progression
Key Tumor Suppressive miRs Playing a Role in CTCL Pathogenesis
Non-Canonical Functions of miRs
Dual Interplay between miRs and Therapeutics Targeting the Epigenome
Findings
10. Conclusions
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