Biology of Childhood Leukaemia Group

Professor Mel Greaves’ Biology of Childhood Leukaemia Group is funded by The Kay Kendall Leukaemia Fund and Leukaemia & Lymphoma Research and seeks to uncover the causes of childhood acute lymphoblastic leukaemia (ALL).

Our group seeks to uncover the pre-clinical natural history, clonal evolution and aetiology of childhood acute lymphoblastic leukaemia (ALL).

Professor Sir Mel Greaves, Biology of Childhood Leukaemia Group

  • Our specialist programme funded by Cancer Research UK is focussed on mouse modelling of the role of the gut microbiome in susceptibility to infection triggered leukaemia.
  • Continued investigation of the genetics of leukaemia in pairs of identical twins (world wide).


Biology of Childhood Leukaemia

Our specialist programme of research (funded by The Kay Kendall Leukaemia Fund and Leukaemia & Lymphoma Research) seeks to uncover the pre-clinical natural history, clonal evolution and aetiology of the major subtype of paediatric leukaemia: childhood acute lymphoblastic leukaemia (ALL).

Individual projects in the portfolio are designed to endorse developmental models for these leukaemias involving pre-natal initiation and a trigger for overt clinical disease involving abnormal immune responses to infection.

We have an extensive network of UK-based and international collaborators providing access to patient samples. Our epidemiological interests are pursued via the UK Children’s Cancer Study Group (UKCCS) and via international cooperation (e.g. Brazil, Hong Kong, Japan and Italy). Our genetic studies on inherited susceptibility to ALL are pursued in collaboration with Professor Richard Houlston and colleagues in the Genetics Section of the Institute of Cancer Research (ICR).

Key review references to group’s work:

  • Greaves MF (2006) Infection, immune responses and the aetiology of childhood leukaemia. Nature Reviews Cancer, 6: 193-203.
  • Greaves MF, Maia AT, Wiemels JL, Ford AM (2003) Leukemia in twins: lessons in natural history. Blood, 102: 2321-2333.
  • Greaves MF, Wiemels J (2003) Origins of chromosome translocations in childhood leukaemia. Nature Reviews Cancer, 3: 639-649.
  • Greaves M (2007) Darwinian medicine: a case for cancer. Nat Rev Cancer, 7: 213-221.
  • Anderson K, Lutz C, van Delft FW, Bateman CM, Guo Y, Colman SM, Kempski H, Moorman AV, Titley I, Swansbury J, Kearney L, Enver T, and Greaves M (2011) Genetic variegation of clonal architecture and propagating cells in leukaemia. Nature, 469: 356-361.
  • Greaves M and Maley C (2012) Clonal evolution in cancer. Nature, 481: 306-313.
  • Greaves M (2015) Evolutionary determinants of cancer. Cancer Discovery, 5: 806-820
  • Pappaemannuil et al (2014). Nature Genetics, 46: 115-125. (See my full list of papers for details)

Greaves M (2018) A causal mechanism for childhood acute lymphoblastic leukaemia. Nature Reviews Cancer, 18: 471-484.

Sir Mel Greaves

Group Leader:

Biology of Childhood Leukaemia Mel Greaves

Professor Sir Mel Greaves is the Founding Director of the ICR Centre for Evolution and Cancer. Professor Greaves is investigating what triggers leukaemia in children. He has received many awards for his work and is a Fellow of the Royal Society, an Honorary Member of the Royal College of Physicians, and a Fellow of the United Kingdom Academy of Medical Sciences.

Researchers in this group

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Phone: +44 20 3437 6074

Email: [email protected]

Location: Sutton

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Phone: +44 20 8722 4066

Email: [email protected]

Location: Sutton

Dr Sureyya Kose .

Phone: +44 20 8722 4674

Email: [email protected]

Location: Sutton

Dr Sureyya Kose recently earned her PhD in Chemistry, investigating the interaction between microbial gene expression and host innate immunity to reveal processes that may lead to cholelithiasis. Presently, her work involves the identification of genetic susceptibility to childhood cancer.

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Phone: +44 20 3437 6387

Email: [email protected]

Location: Sutton

Sir Mel Greaves's group have written 50 publications

Most recent new publication 18/3/2008

See all their publications

Recent discoveries from this group

07/04/21

Deformed cells in the bone marrow, typical of chronic leukaemia (photo: Difu Wu/CC BY-SA 3.0)

Image: Deformed cells in the bone marrow, typical of chronic leukaemia. Photo: Difu Wu

Death from infection – the leading cause of death for patients with a common type of leukaemia – is linked to specific gene mutations, a new study has found.

Testing for these mutations could be used to identify patients at a higher risk of dying from infection and inform disease management strategies.

The study, published in the journal Leukemia and led by scientists at The Institute of Cancer Research, London, found that patients with chronic lymphocytic leukaemia (CLL) who carried one or more mutations in the BRAF, FBXW7, NRAS or XPO1 genes were more likely to die from contracting an infection than those without.

It was the first study to analyse the causes of death in CLL patients in detail – and, in particular, to look at the causes of death from infection, which is the leading cause of deaths associated with CLL, accounting for around half.

Cancer and infectious disease

Screening CLL patients for the presence of any of these four mutations could help identify those at greater risk of dying from infection, as well as inform ways to carefully manage their chances of infection – for example, by choosing appropriate CLL therapies.

Infection causes death in CLL patients, largely due to the dysregulation and deficiency of their immune system by the disease or by treatment. For example, defective T-cells and B-cells can increase the chances of infection, and immunosuppressive therapies can make patients more susceptible to infectious diseases.

This is especially concerning with the emergence of Covid-19 as it presents another possible route to infection, putting CLL patients at risk.

Chronic lymphocytic leukaemia trial

In the new study, researchers at the ICR and the University of Southampton analysed the causes of death of patients enrolled in the LRF CLL4 trial – which established the benefit of the drug fludarabine in combination with cyclophosphamide, compared with conventional chlorambucil therapy.

The trial collected data from 777 CLL patients from 1999 to 2004, with an average follow-up time of 13 years, and its initial findings were published in the Lancet in 2007.

Of the 600 patients who died of a known cause, 43% died of infection, the new study found – either as a primary or secondary cause. Comparing blood samples from patients who died from infection versus other causes, the team then found that although there were no differences between the two groups in terms of demographics and prognostic markers, such as disease stage, there were several distinct genetic changes specifically linked to those who had died from infection.

Increased infection death risk

Of the genes analysed, mutations in the BRAF, FBXW7, NRAS and XPO1 genes were significantly associated with death from infection, with 69 per cent of patients carrying one or more of these mutations dying from infection compared to 39 per cent who lacked any of the mutations.

The study was largely funded by the charity Blood Cancer UK, formerly the Leukaemia Research Fund (LRF).

Monica Else, Honorary Senior Scientific Officer in the Division of Molecular Pathology at the ICR, and one of the lead authors of the study, said:

“Our study found a link between certain gene mutations and deaths from infection in CLL, which could help to inform future treatment strategies for patients with these infections. It also raises the intriguing possibility of a relationship between these genes and the origin of infections in leukaemia.

“If these mutations turn out to be important in the origin of infections, or in the way that CLL develops as a result of its interaction with infections, then it will be very exciting. It is very possible that infections play a role in the way CLL develops and if so, these mutations might be a part of that.”

Daniel Catovsky, Professor Emeritus at the ICR, and formerly Team Leader in Haemato-Oncology, was the Principal Investigator of the CLL4 trial. He said:

“Infections are a common cause of death in chronic lymphocytic leukaemia, a disease which otherwise patients can live with for many years with relatively few ill effects. Although our trial initially focused, successfully, on answering the question of which is the most effective cancer drug treatment for CLL, the results have now shed new light on the management of infection – a crucial question for patients, and all the more so now in the era of Covid-19.”