Cancers (Feb 2021)

Apoptotic Blocks in Primary Non-Hodgkin B Cell Lymphomas Identified by BH3 Profiling

  • Ryan N. Rys,
  • Claudia M. Wever,
  • Dominique Geoffrion,
  • Christophe Goncalves,
  • Artin Ghassemian,
  • Eugene Brailovski,
  • Jeremy Ryan,
  • Liliana Stoica,
  • Josée Hébert,
  • Tina Petrogiannis-Haliotis,
  • Svetlana Dmitrienko,
  • Saul Frenkiel,
  • Annette Staiger,
  • German Ott,
  • Christian Steidl,
  • David W. Scott,
  • Pierre Sesques,
  • Sonia del Rincon,
  • Koren K. Mann,
  • Anthony Letai,
  • Nathalie A. Johnson

DOI
https://doi.org/10.3390/cancers13051002
Journal volume & issue
Vol. 13, no. 5
p. 1002

Abstract

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To determine causes of apoptotic resistance, we analyzed 124 primary B cell NHL samples using BH3 profiling, a technique that measures the mitochondrial permeabilization upon exposure to synthetic BH3 peptides. Our cohort included samples from chronic lymphocytic leukemia (CLL), follicular lymphoma (FL), diffuse large B-cell lymphoma (DLBCL), high-grade B cell lymphoma with translocations in MYC and BCL2 (HGBL-DH), mantle cell lymphoma (MCL) and marginal zone lymphoma (MZL). While a large number of our samples displayed appropriate responses to apoptosis-inducing peptides, pro-apoptotic functional defects, implicating BAX, BAK, BIM or BID, were seen in 32.4% of high-grade NHLs (12/37) and in 3.4% of low-grade NHLs (3/87, p p < 0.05). Overall, in primary NHLs expressing BCL2 that have no defects in pro-apoptotic signaling, a poor response to venetoclax is primarily due to the presence of MCL1, which may be overcome by combining venetoclax with doxorubicin and vincristine-based chemotherapy or with other anti-microtubule inhibitors.

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