Genetic Modeling of B-cell State Transitions for Rational Design of Lymphoma Therapies

Author:

Leveille Etienne12ORCID,Kothari Shalin12ORCID,Müschen Markus123ORCID

Affiliation:

1. 1Center of Molecular and Cellular Oncology, Yale University, New Haven, Connecticut.

2. 2Department of Internal Medicine, Yale University, New Haven, Connecticut.

3. 3Department of Immunobiology, Yale University, New Haven, Connecticut.

Abstract

Summary:The use of genomic data to analyze primary endpoints for clinical trials in diffuse large B-cell lymphomas (DLBCL) significantly improved the development of rational drug combinations for genetically defined patient subsets. Recent genetic mouse models and their ability to recapitulate transitions between germinal center exit and memory B-cell characteristics in DLBCL will accelerate the development of rationale-based clinical trials.See related article by Flümann et al., p. 78 (3).See related article by Venturutti et al., (5).

Publisher

American Association for Cancer Research (AACR)

Subject

General Medicine

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