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Acute myeloid leukaemia in its niche: the bone marrow microenvironment in acute myeloid leukaemia

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posted on 2023-06-07, 07:20 authored by E E Ladikou, H Sivaloganathan, Andrea PepperAndrea Pepper, Timothy ChevassutTimothy Chevassut
Purpose of Review Acute myeloid leukaemia (AML) is a heterogeneous malignancy for which treatment options remain suboptimal. It is clear that a greater understanding of the biology of the AML niche will enable new therapeutic strategies to be developed in order to improve treatment outcomes for patients. Recent Findings Recent evidence has highlighted the importance of the bone marrow microenvironment in protecting leukaemia cells, and in particular leukaemic stem cells from chemotherapy-induced cell death. This includes mesenchymal stem cells supporting growth and preventing apoptosis, and altered action and secretion profiles of other niche components including adipocytes, endothelial cells and T cells. Summary Here, we provide a detailed overview of the current understanding of the AML bone marrow microenvironment. Clinical trials of agents that mobilise leukaemic stem cells from the bone marrow are currently ongoing and show early promise. Future challenges will involve combining these novel therapies targeted at the AML niche with conventional chemotherapy treatment.

Funding

How does SARS CoV-2 infect blood vessels?; G3146; UK RESEARCH AND INNOVATION; MR/V036750/1

Drug-induced selective lethality in populations of DNMT3A knockdown cells; G2782; WELLCOME TRUST; 218435/Z/19/Z

Mining the Wnt signalling-responsive surfaceome for drug targets in acute myeloid leukaemia; G3090; WELLCOME TRUST

In vitro modelling and therapeutic targeting of tumour cell migration in chronic lymphocytic leukaemia.; G2544; BLOODWISE

SUSSEX CANCER FUND FOR TREATMENT AND RESEARCH; G3106; SUSSEX CANCER FUND FOR TREATMENT AND RESEARCH

History

Publication status

  • Published

File Version

  • Published version

Journal

Current Oncology Reports

ISSN

1523-3790

Publisher

Springer

Volume

22

Page range

1-9

Article number

a27

Department affiliated with

  • Clinical and Experimental Medicine Publications

Full text available

  • No

Peer reviewed?

  • Yes

Legacy Posted Date

2020-06-23

First Open Access (FOA) Date

2020-06-23

First Compliant Deposit (FCD) Date

2020-06-23

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