Literature DB >> 28275912

Mechanisms of Resistance to Targeted Therapies in Chronic Lymphocytic Leukemia.

Francesca Arruga1, Silvia Deaglio2,3.   

Abstract

Even if treatment options for Chronic Lymphocytic Leukemia (CLL) patients have changed dramatically in the past few years, with the approval of targeted therapeutic agents, the disease remains incurable. Beside intrinsic genetic features characterizing the leukemic cell, signals coming from the microenvironment have a key role in promoting cell survival and in protecting CLL cells from the action of drugs. Consequently, the identification of previously unrecognized genetic lesions is important in risk-stratification of CLL patients and is progressively becoming a critical tool for choosing the best therapeutic strategy. Significant efforts have also been dedicated to define microenvironment-dependent mechanisms that sustain leukemic cells favoring survival, proliferation, and accumulation of additional genetic lesions. Furthermore, understanding the molecular and biological mechanisms, potentially driving disease progression and chemoresistance, is the first step to design therapies that could be effective in high-risk patients. Significant progress has been made in the identification of the different mechanisms through which patients relapse after "new" and "old" therapies. These studies have led to the development of targeted strategies to overcome, or even prevent, resistance through the design of novel agents or their combination.In this chapter we will give an overview of the main therapeutic options for CLL patients and review the mechanisms of resistance responsible for treatment failure. Potential strategies to overcome or prevent resistance will be also discussed.

Entities:  

Keywords:  Chronic lymphocytic leukemia; Resistance; Target therapy

Mesh:

Substances:

Year:  2018        PMID: 28275912     DOI: 10.1007/164_2017_12

Source DB:  PubMed          Journal:  Handb Exp Pharmacol        ISSN: 0171-2004


  4 in total

Review 1.  Ectonucleotidases in Blood Malignancies: A Tale of Surface Markers and Therapeutic Targets.

Authors:  Tiziana Vaisitti; Francesca Arruga; Giulia Guerra; Silvia Deaglio
Journal:  Front Immunol       Date:  2019-10-04       Impact factor: 7.561

2.  Pharmacological modulation of Kv1.3 potassium channel selectively triggers pathological B lymphocyte apoptosis in vivo in a genetic CLL model.

Authors:  Filippo Severin; Andrea Urbani; Tatiana Varanita; Magdalena Bachmann; Michele Azzolini; Veronica Martini; Marco Pizzi; Angelo Paolo Dei Tos; Federica Frezzato; Andrea Mattarei; Paolo Ghia; Maria Teresa Sabrina Bertilaccio; Erich Gulbins; Cristina Paradisi; Mario Zoratti; Gianpietro Carlo Semenzato; Luigi Leanza; Livio Trentin; Ildiko Szabò
Journal:  J Exp Clin Cancer Res       Date:  2022-02-16

Review 3.  Targeting the Adenosinergic Axis in Chronic Lymphocytic Leukemia: A Way to Disrupt the Tumor Niche?

Authors:  Tiziana Vaisitti; Francesca Arruga; Silvia Deaglio
Journal:  Int J Mol Sci       Date:  2018-04-12       Impact factor: 5.923

4.  Targeting of the A2A adenosine receptor counteracts immunosuppression in vivo in a mouse model of chronic lymphocytic leukemia.

Authors:  Francesca Arruga; Sara Serra; Nicoletta Vitale; Giulia Guerra; Andrea Papait; Benjamin Baffour Gyau; Francesco Tito; Dimitar Efremov; Tiziana Vaisitti; Silvia Deaglio
Journal:  Haematologica       Date:  2021-05-01       Impact factor: 9.941

  4 in total

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