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The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.

Genetics of diffuse large B-cell lymphoma

Open access
Pasqualucci, Laura, Dalla-Favera, Riccardo·2018·Blood

Abstract

Diffuse large B-cell lymphoma (DLBCL), the most frequent subtype of lymphoid malignancy, remains a significant clinical challenge, as ∼30% of patients are not cured. Over the past decade, remarkable progress has been made in the understanding of the pathogenesis of this disease, spurred by the implementation of powerful genomic technologies that enabled the definition of its genetic and epigenetic landscape. These studies have uncovered a multitude of genomic alterations that contribute to the initiation and maintenance of the tumor clone by disrupting biological functions known to be critical for the normal biology of its cells of origin, germinal center B cells. The identified alterations involve epigenetic remodeling, block of differentiation, escape from immune surveillance, and the constitutive activation of several signal transduction pathways. This wealth of new information offers unique opportunities for the development of improved diagnostic and prognostic tools that could help guide the clinical management of DLBCL patients. Furthermore, a number of the mutated genes identified are potentially actionable targets that are currently being explored for the development of novel therapeutic strategies. This review summarizes current knowledge of the most common genetic alterations associated with DLBCL in relation to their functional impact on the malignant transformation process, and discusses their clinical implications for mechanism-based therapeutics.

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Crossref · 10.1182/blood-2017-11-764332

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Metadata

Authors
Pasqualucci, L., & Dalla-Favera, R.
Venue
Blood
Published
2018-05-24
Volume
131
Issue
21
Pages
2307-2319
ISSN
  • 0006-4971 (ISSN-L)
  • 1528-0020
OpenAlex
W2800080453
Cited by
282
References
11
FWCI
20.41
Type
journal article
Language
en
Open access
green

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