Paediatric Solid Tumour Biology and Therapeutics Group

Professor Louis Chesler’s group is investigating the genetic causes for the childhood cancers, neuroblastoma, medulloblastoma and rhabdomyosarcoma. 

Research, projects and publications in this group

Our group's aim is to improve the treatment and survival of children with neuroblastoma, medulloblastoma and rhabdomyosarcoma.

The goal of our laboratory is to improve the treatment and survival of children with neuroblastoma, medulloblastoma and rhabdomyosarcoma, three paediatric solid tumours in which high-risk patient cohorts can be defined by alterations in a single oncogene. We focus on the role of the MYCN oncogene, since aberrant expression of MYCNis very significantly associated with high-risk in all three diseases and implies that they may have a common cell-of-origin.

Elucidating the molecular signalling pathways that control expression of the MYCN oncoprotein and targeting these pathways with novel therapeutics is a major goal of the laboratory. We use a variety of innovative preclinical drug development platforms for this purpose.

Technologically, we focus on genetically engineered cancer models incorporating novel imaging (optical and fluorescent) modalities that can be used as markers to monitor disease progression and therapeutic response.

Our group has several key objectives:

  • Mechanistically dissect the role of the MYCN oncogene, and other key oncogenic driver genes in poor-outcome paediatric solid tumours (neuroblastoma, medulloblastoma, rhabdomyosarcoma).
  • Develop novel therapeutics targeting MYCN oncoproteins and other key oncogenic drivers
  • Develop improved genetic cancer models dually useful for studies of oncogenesis and preclinical development of novel therapeutics.
  • Use such models to develop and functionally validate optical imaging modalities useful as surrogate markers of tumour progression in paediatric cancer.

Professor Louis Chesler

Clinical Senior Lecturer/Group Leader:

Paediatric Solid Tumour Biology and Therapeutics Professor Louis Chesler (Profile pic)

Professor Louis Chesler is working to understand the biology of children’s cancers and use that information to discover and develop new personalised approaches to cancer treatment. His work focuses on improving the understanding of the role of the MYCN oncogene.

Researchers in this group

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Email: [email protected]

Location: Sutton

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Phone: +44 20 3437 6124

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Location: Sutton

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Email: [email protected]

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Location: Sutton

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Location: Sutton

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Phone: +44 20 3437 6118

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Location: Sutton

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Email: [email protected]

Location: Sutton

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Location: Sutton

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OrcID: 0000-0003-3977-7020

Phone: +44 20 3437 6109

Email: [email protected]

Location: Sutton

I obtained an MSci in Biochemistry from the University of Glasgow in 2018. In October 2018 I joined the labs of Dr Michael Hubank and Professor Andrea Sottoriva to investigate the use of liquid biopsy to monitor clonal frequency and emergence of resistance mutations in paediatric cancers.

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Email: [email protected]

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Location: Sutton

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Email: [email protected]

Location: Sutton

Professor Louis Chesler's group have written 113 publications

Most recent new publication 4/2025

See all their publications

Vacancies in this group

Working in this group

Postdoctoral Training Fellow

  • Chelsea
  • Structural Biology
  • Salary Range: £45,600 - £55,000 per annum
  • Fixed term

Under the leadership of Claudio Alfieri, we are seeking to appoint a Postdoctoral Training Fellow to join the Molecular Mechanisms of Cell Cycle Regulation Group at the Chester Beatty Laboratories, Fulham Road in London. This project aims to investigate the molecular mechanisms of cell cycle regulation by macromolecular complexes involved in cell proliferation decisions, by combining genome engineering, proteomics and in situ structural biology. For general information on Post Doc's at The ICR can be found here. Key Requirements The successful candidate must have a PhD in cellular biochemistry and experience in Cryo-EM and CLEM is desirable. The ICR has a workforce agreement stating that Postdoctoral Training Fellows can only be employed for up to 7 years as PDTF at the ICR, providing total postdoctoral experience (including previous employment at this level elsewhere) does not exceed 7 years Department/Directorate Information: The candidate will work in the Molecular Mechanisms of Cell Cycle Regulation Group within the ICR Division of Structural Biology headed by Prof. Laurence Pearl and Prof. Sebastian Guettler. The division has state-of-the-art facilities for protein expression and biophysics/x-ray crystallography, in particular the Electron Microscopy Facility is equipped with a Glacios 200kV with Falcon 4i detector with Selectris energy filter and the ICR has access to Krios microscopes via eBIC and the LonCEM consortium. We encourage all applicants to access the job pack attached for more detailed information regarding this role. For an informal discussion regarding the role, please contact Claudio Alfieri via Email on [email protected]

Data Scientist

  • Sutton
  • Cell and Molecular Biology
  • Salary Range: £39,805 to £49,023 per annum
  • Fixed term

Under the guidance of Professor Trevor Graham, we are seeking to recruit a Data Scientist to support Data Science research across the ICR. The successful candidate will particularly work on the analysis of spatial data including multiplex immunohistochemistry, H&Es and spatial transcriptomics. About you The successful candidate must have: A PhD in quantitative subject, or likely to be awarded PhD in the near future. Research experience equivalent to PhD level will be considered. Undergraduate degree, or Masters or equivalent in a quantitative subject. Skills in bioinformatics computing coding, in languages including R, Python and other scripting languages as is appropriate. Experience of using high performance computing (HPC) systems for scientific computing. Experience of computational biology research methodologies pertinent to the role. Department/Directorate Information The Data Science Committee is chaired by Professor Trevor Graham, providing academic leadership of data science at the ICR to maximise the impact of our cancer research, by applying innovative data science and computation tools (in addition to our traditional areas of strength) to tackle the important cancer questions and ensuring infrastructure is considered to enable this. What we offer A dynamic and supportive research environment Access to state-of-the-art facilities and professional development opportunities Collaboration with leading researchers in the field Competitive salary and pension We encourage all applicants to access the job pack attached for more detailed information regarding this role. For an informal discussion regarding the role, please contact Prof Trevor Graham [email protected].

Industrial partnership opportunities with this group

Opportunity: A novel test for predicting future cancer risk in patients with inflammatory bowel disease

Commissioner: Professor Trevor Graham

Recent discoveries from this group

20/06/25

Scientists have developed a tool that can predict how bowel cancer adapts to treatment – helping researchers to design new personalised drugs that will keep patients living well for longer. 

A team from the Institute of Cancer Research, London, and Queen Mary University of London have designed a new technology that uses evolutionary biology to measure and predict how cancer cells will evolve when they are exposed to a new treatment.

Bowel cancer is the fourth most common cancer in the UK. There are around 44,100 new bowel cancer cases in the UK every year, or around 120 every day.  Most bowel cancers are treated with chemotherapies and these treatments haven’t changed in almost 50 years.

Patients with late-stage disease typically die from drug resistance – when the cancer stops responding to treatment.

What causes drug resistance?

Drug resistance is caused by molecular changes in cancer cells that renders the treatment ineffective. Understanding exactly how this resistance develops will allow researchers design new and better drugs that target the mechanisms of resistance – ensuring cancer is kept at bay for longer. It will also allow clinicians to use existing drugs in the optimal way – altering doses if necessary.  

There are two routes that cancer cells can take to escape a drug’s action, but until now, it has been very hard to tell them apart.

In research published in the journal Nature Communications, the team from the Centre for Evolution and Cancer at The Institute of Cancer Research (ICR), and funded by the Wellcome Trust and Cancer Research UK, tracked bowel cancer cells as they evolved resistance to chemotherapy.

Together with colleagues from Queen Mary University of London, the researchers used mathematical modelling to pinpoint when resistance to the drug developed. They could then determine whether resistance was caused by a rare genetic mutation in one cell that was copied as the cell divided, or whether there was a non-genetic change responsible.

Helping to design personalised drugs

The researchers have now turned their method, called EIRAs (Evolutionary Informed Resistance Assays), into a tool that can be adopted into the process of developing new medicines. By using EIRAS, they hope that new personalised drugs can be designed which target the route that a patients’ tumour has taken to evolve resistance.

The researchers are seeking commercial partners to further progress this work, as well as working with colleagues in the ICR’s Centre for Cancer Drug Discovery. A patent has been submitted for the technology, which the researchers believe could be used to support the development of a number of cancer drugs – they have already begun exploring its use for ovarian and breast cancer.

'Treatment resistance is a long-standing problem that we are desperate to solve'

Professor Trevor Graham, Professor of Genomics and Evolution and Director of the Centre for Evolution and Cancer at The Institute of Cancer Research, London, said:

“Just like bacteria evolve resistance to antibiotics, cancer cells can evolve resistance to chemotherapy, making treatment less effective. This treatment resistance is a long-standing problem that we are desperate to solve. Cancers may respond well for a while, but sadly then they usually become resistant and the drug stops working.

“By studying bowel cancer cells over time as we treat them with chemotherapy, we have been able to develop a machine learning technology that can unpick how and when these cells become resistant. We hope this information will allow us to design new, personalised drugs – ones that target these changes so that the cancer responds to treatment. We also believe we can use the technology to learn how to alter the dose of existing drugs, to keep them working for longer.

“I’m excited to work with colleagues and partners – including those in the ICR’s Centre for Cancer Drug Discovery – to implement this technology, and to bring more treatment options to patients living with cancer.”

Dr Freddie Whiting, postdoctoral researcher at The Institute of Cancer Research, London, said: 

“With this new computational method of measuring how cancer cells evolve during treatment, we are hopeful that it will be easier to identify those that minimise the evolution of drug resistance. I am excited to see our platform, Evolutionary Informed Resistance Assays (EIRAs), incorporated into the drug discovery process to speed up the development of drugs that lead to the best possible response in patients.”

'We are constantly searching for ways to halt cancer’s growth when treatments stop working'

Professor Kristian Helin, Chief Executive of The Institute of Cancer Research, London, said:

“As cancer researchers, we are constantly searching for ways to halt cancer’s growth when treatments stop working. This work will help us to identify new targets to tackle cancer once resistance develops.

“The research brings together ideas in machine learning, cancer evolution, and drug discovery. The Institute of Cancer Research has an unrivalled track record of drug discovery, and I look forward to seeing this technology progress, through our Centre for Cancer Drug Discovery and through collaborations with partners, to drive the development of treatments that benefit patients for even longer.”

Professor Richard Nichols, Professor of Evolutionary Genetics in the School of Biological and Behavioural Sciences at Queen Mary University London, said:

“These advances have come from treating cancer cells’ resistance to chemotherapy as a question about evolution.  We asked whether their resistance has a genetic basis, building on methods that were first developed to resolve disputes among biologists about the colour patterns of snails. The success of this project shows the value of cross-fertilization of ideas, sometimes between subject areas that seem distantly related.”

Morag Foreman, Head of Discovery Researchers at The Wellcome Trust said:

“Every cancer is unique and will not respond to treatments in the same way. Recognising how resistance develops on a case-by-case basis means we can tailor treatment plans for individuals to ensure they continue to be effective, adding another tool to help us better understand cancer as a disease. At Wellcome, we’re pleased to have supported this research, which is an excellent example of how interdisciplinary approaches are essential to tackling the pressing health issues we face.”