Skip to main content
Top
Published in: BMC Cancer 1/2021

Open Access 01-12-2021 | Acute Lymphoblastic Leukemia | Research

Intrinsic and extrinsic apoptosis responses in leukaemia cells following daunorubicin treatment

Authors: Hussain Mubarak Al-Aamri, Helen R. Irving, Christopher Bradley, Terri Meehan-Andrews

Published in: BMC Cancer | Issue 1/2021

Login to get access

Abstract

Background

Daunorubicin is used clinically in the treatment of myeloma, acute lymphatic and myelocytic leukaemia. The toxic lesions caused by daunorubicin induce various modes of cell death, including apoptosis. Apoptosis is highly regulated programmed cell death that can be initiated mainly via two pathways, through death receptors (extrinsic) or involvement of the mitochondria (intrinsic). Induction of apoptosis via these pathways has been alluded following treatment with daunorubicin, but never compared in acute lymphoblastic leukaemia over a time course.

Methods

This study investigated the mechanisms of daunorubicin induced apoptosis in the treatment of CCRF-CEM, MOLT-4 (acute T-lymphoblastic leukaemia) and SUP-B15 (acute B-lymphoblastic leukaemia) cells. Cells were treated with daunorubicin for 4 h, and then placed in recovery medium (without daunorubicin) for 4 h, 12 h and 24 h. Apoptotic response was analysing using annexin-V expression, caspase activity, mitochondrial membrane potential change and an array to detect 43 apoptotic proteins.

Results

Daunorubicin induced apoptosis in all leukemic cell lines, but with different levels and duration of response. Both apoptosis levels and caspase activity increased after four hours recovery then declined in CCRF-CEM and MOLT-4 cells. However, SUP-B15 cells displayed initially comparable levels but remained elevated over the 24 h assessment period. Changes in mitochondrial membrane potential occurred in both MOLT-4 and CCRF-CEM cells but not in SUP-B15 cells. Expression of apoptotic proteins, including Bcl-2, Bax, caspase 3 and FADD, indicated that daunorubicin potentially induced both extrinsic and intrinsic apoptosis in both CCRF-CEM and MOLT-4 cells, but only extrinsic apoptosis in SUP-B15 cells.

Conclusions

This study describes variations in sensitivities and timing of apoptotic responses in different leukaemia cell lines. These differences could be attributed to the lack of functional p53 in coordinating the cells response following cytotoxic treatment with daunorubicin, which appears to delay apoptosis and utilises alternative signalling mechanisms that need to be further explored.
Appendix
Available only for authorised users
Literature
2.
go back to reference Stojak M, Mazur L, Opydo-Chanek M, Lukawska M, Oszczapowicz I. In vitro induction of apoptosis and necrosis by new derivatives of daunorubicin. Anticancer Res. 2013;33(10):4439–43.PubMed Stojak M, Mazur L, Opydo-Chanek M, Lukawska M, Oszczapowicz I. In vitro induction of apoptosis and necrosis by new derivatives of daunorubicin. Anticancer Res. 2013;33(10):4439–43.PubMed
3.
go back to reference Chikayama S, Kimura S, Kobayashi Y, Abe T, Maekawa T, Kondo M. Effects of daunorubicin on cell growth, cell cycle and induction of apoptosis in HL-60 cells. Haematologia. 1998;29(2):115–21.PubMed Chikayama S, Kimura S, Kobayashi Y, Abe T, Maekawa T, Kondo M. Effects of daunorubicin on cell growth, cell cycle and induction of apoptosis in HL-60 cells. Haematologia. 1998;29(2):115–21.PubMed
8.
go back to reference Bouillet P, Strasser A. BH3-only proteins - evolutionarily conserved proapoptotic Bcl-2 family members essential for initiating programmed cell death. J Cell Sci. 2002;115(Pt 8):1567–74.PubMed Bouillet P, Strasser A. BH3-only proteins - evolutionarily conserved proapoptotic Bcl-2 family members essential for initiating programmed cell death. J Cell Sci. 2002;115(Pt 8):1567–74.PubMed
26.
go back to reference Chang H-Y, Huang H-C, Huang T-C, Yang P-C, Wang Y-C, Juan H-F. Flow Cytometric detection of mitochondrial membrane potential. Bio-protocol. 2013;3(8):e430. Chang H-Y, Huang H-C, Huang T-C, Yang P-C, Wang Y-C, Juan H-F. Flow Cytometric detection of mitochondrial membrane potential. Bio-protocol. 2013;3(8):e430.
30.
31.
go back to reference Brown LM, Hanna DT, Khaw SL, Ekert PG. Dysregulation of BCL-2 Family Proteins by Leukaemia Fusion Genes. J Biol Chem. 2017:jbc. R117. 799056. Brown LM, Hanna DT, Khaw SL, Ekert PG. Dysregulation of BCL-2 Family Proteins by Leukaemia Fusion Genes. J Biol Chem. 2017:jbc. R117. 799056.
39.
go back to reference Kantari C, Walczak H. Caspase-8 and bid: caught in the act between death receptors and mitochondria. Biochimica et Biophysica Acta (BBA)-molecular. Cell Res. 2011;1813(4):558–63. Kantari C, Walczak H. Caspase-8 and bid: caught in the act between death receptors and mitochondria. Biochimica et Biophysica Acta (BBA)-molecular. Cell Res. 2011;1813(4):558–63.
41.
go back to reference Pennarun B, Meijer A, de Vries EG, Kleibeuker JH, Kruyt F, de Jong S. Playing the DISC: turning on TRAIL death receptor-mediated apoptosis in cancer. Biochimica et Biophysica Acta (BBA)-Reviews on Cancer. 2010;1805(2):123–40.CrossRef Pennarun B, Meijer A, de Vries EG, Kleibeuker JH, Kruyt F, de Jong S. Playing the DISC: turning on TRAIL death receptor-mediated apoptosis in cancer. Biochimica et Biophysica Acta (BBA)-Reviews on Cancer. 2010;1805(2):123–40.CrossRef
Metadata
Title
Intrinsic and extrinsic apoptosis responses in leukaemia cells following daunorubicin treatment
Authors
Hussain Mubarak Al-Aamri
Helen R. Irving
Christopher Bradley
Terri Meehan-Andrews
Publication date
01-12-2021
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2021
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/s12885-021-08167-y

Other articles of this Issue 1/2021

BMC Cancer 1/2021 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine