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Cited by 302

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

Genetic lesions associated with chronic lymphocytic leukemia transformation to Richter syndrome

Open access
Fabbri, Giulia, Khiabanian, Hossein, Holmes, Antony B., Wang, Jiguang, Messina, Monica, Mullighan, Charles G., Pasqualucci, Laura, Rabadan, Raul, Dalla-Favera, Riccardo·2013·Journal of Experimental Medicine

Abstract

Richter syndrome (RS) derives from the rare transformation of chronic lymphocytic leukemia (CLL) into an aggressive lymphoma, most commonly of the diffuse large B cell lymphoma (DLBCL) type. The molecular pathogenesis of RS is only partially understood. By combining whole-exome sequencing and copy-number analysis of 9 CLL-RS pairs and of an extended panel of 43 RS cases, we show that this aggressive disease typically arises from the predominant CLL clone by acquiring an average of ∼20 genetic lesions/case. RS lesions are heterogeneous in terms of load and spectrum among patients, and include those involved in CLL progression and chemorefractoriness (TP53 disruption and NOTCH1 activation) as well as some not previously implicated in CLL or RS pathogenesis. In particular, disruption of the CDKN2A/B cell cycle regulator is associated with ∼30% of RS cases. Finally, we report that the genomic landscape of RS is significantly different from that of de novo DLBCL, suggesting that they represent distinct disease entities. These results provide insights into RS pathogenesis, and identify dysregulated pathways of potential diagnostic and therapeutic relevance.

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Metadata

Authors
Fabbri, G., Khiabanian, H., Holmes, A. B., Wang, J., Messina, M., Mullighan, C. G., Pasqualucci, L., Rabadan, R., & Dalla-Favera, R.
Venue
Journal of Experimental Medicine
Published
2013-10-14
Volume
210
Issue
11
Pages
2273-2288
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2129650489
Cited by
302
References
11
FWCI
9.47
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Genetic lesions associated with chronic lymphocytic leukemia transformation to Richter syndrome. https://app.cochat.ai/papers/10.1084/jem.20131448
The paper
Fabbri, G., Khiabanian, H., Holmes, A. B., Wang, J., Messina, M., Mullighan, C. G., Pasqualucci, L., Rabadan, R., & Dalla-Favera, R. (2013). Genetic lesions associated with chronic lymphocytic leukemia transformation to Richter syndrome. Journal of Experimental Medicine. https://doi.org/10.1084/jem.20131448

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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