4.4 Article

The prohibitin-binding compound fluorizoline induces apoptosis in chronic lymphocytic leukemia cells through the upregulation of NOXA and synergizes with ibrutinib, 5-aminoimidazole-4-carboxamide riboside or venetoclax

Journal

HAEMATOLOGICA
Volume 102, Issue 9, Pages 1587-1593

Publisher

FERRATA STORTI FOUNDATION
DOI: 10.3324/haematol.2016.162958

Keywords

-

Categories

Funding

  1. Ministerio de Economia y Competitividad [SAF2013-41611-R, BQU-CTQ2015-67870-P]
  2. Instituto de Salud Carlos III [RTICC RD12/0036/0029]
  3. Fundacio Bosch i Gimpera [AVCRI-PPV022-08]
  4. AGAUR-Generalitat de Catalunya [2014SGR935, 2014SGR137]
  5. Ministerio de Economia y Competitividad
  6. Universitat de Barcelona

Ask authors/readers for more resources

Fluorizoline is a new synthetic molecule that induces apoptosis by selectively targeting prohibitins. In the study herein, the pro-apoptotic effect of fluorizoline was assessed in 34 primary samples from patients with chronic lymphocytic leukemia. Fluorizoline induced apoptosis in chronic lymphocytic leukemia cells at concentrations in the low micromolar range. All primary samples were sensitive to fluorizoline irrespective of patients' clinical or genetic features, whereas normal T lymphocytes were less sensitive. Fluorizoline increased the protein levels of the pro-apoptotic B-cell lymphoma 2 family member NOXA in chronic lymphocytic leukemia cells. Furthermore, fluorizoline synergized with ibrutinib, 5-aminoimidazole-4-carboxamide riboside or venetoclax to induce apoptosis. These results suggest that targeting prohibitins could be a new therapeutic strategy for chronic lymphocytic leukemia.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available