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

Email: [email protected]

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Phone: +44 20 3437 3617

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Location: Sutton

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Phone: +44 20 8722 4186

Email: [email protected]

Location: Sutton

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Phone: +44 20 3437 3501

Email: [email protected]

Location: Sutton

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Email: [email protected]

Location: Sutton

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Phone: +44 20 8722 4361

Email: [email protected]

Location: Sutton

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Email: [email protected]

Location: Sutton

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Phone: +44 20 3437 6118

Email: [email protected]

Location: Sutton

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Phone: +44 20 3437 6021

Email: [email protected]

Location: Sutton

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Phone: +44 20 3437 6196

Email: [email protected]

Location: Sutton

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Phone: +44 20 3437 6258

Email: [email protected]

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Email: [email protected]

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]

Location: Sutton

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Email: [email protected]

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]

Research Group Leader, ICR Clinical Trials and Statistics Unit (ICR-CTSU)

  • Sutton
  • Clinical Trials and Statistics Unit
  • Salary: From £66,092 pa
  • Permanent

Role Summary The Group Leader will lead a component of ICR-CTSU’s portfolio of clinical trials research. The post holder will further develop and grow the portfolio in line with ICR-CTSU’s overall strategy and take responsibility for a number of ongoing trials as well as the development of new trials. We seek an experienced biostatistician with a strong research interest in clinical trials methodology and a passion for direct involvement in the oversight and leadership of academic clinical trials. The successful candidate will work closely with the Director of ICR-CTSU to further enhance the Unit’s internationally recognised strength in clinical trial design, conduct and analysis. The post holder will be expected to make a substantial independent intellectual contribution to clinical trials projects and be proactive in leading and contributing to broad initiatives that enhance the overall effectiveness of ICR-CTSU. The appointee will contribute to the overall scientific life of the ICR including the newly established ICR/Royal Marsden Hospital’s Centre for Trials and Population Data Science, by providing mentorship to more junior colleagues and acting as an academic leader. We seek an individual who will work closely and collaboratively with other faculty/Group Leaders at ICR and with international/national key opinion leaders to extend the breadth and depth of ICR-CTSU’s biologically rich clinical trials portfolio. In partnership with clinical opinion leaders, s/he will generate research funds to conduct and deliver clinical trials research at the international forefront. Presentation at national and international conferences, production of top-quality research outputs and substantial professional contribution to wider clinical trial network bodies are expected. Enthusiasm for team-based science in a collaborative interdisciplinary environment is essential. The appointment will be based on track record and the ability and willingness to engage in team science. The successful appointee will have access to ICR’s successful PhD training programme and core facilities. Key Requirements Higher degree (MSc or PhD) in medical statistics/biostatistics or an allied field (e.g. public health, epidemiology, data science) with relevant work experience Significant experience as a clinical trials, medical or bio-statistician within the academic or commercial sector A desire to apply existing and novel statistical methods to the requirements of a diverse range of statistical problems A broad understanding of cancer research Ability to lead a Clinical Trials Unit based research group As part of your online application, you will be required to upload your full CV which will pre-populate your application form, you will also be asked to attach the following documents and failure to do so will mean your application cannot be considered on this occasion: Lists of major publications, achievements, research grants and distinctions. A PDF of a maximum of five key publications, or other research outputs (e.g. patents) that best demonstrate previous productivity or a single document giving hyperlinks to these outputs. You must also complete the personal statement section of the application form in the format of a cover letter including the names and contact details of three academic referees Department/Directorate Information: Division of Clinical Studies Clinical Trials and Statistics Unit (ICR-CTSU) The ICR-CTSU is a Cancer Research UK-funded, internationally recognised methodologist led clinical trials unit, providing cancer-focused clinical trial research expertise. We lead pioneering, efficient, high-quality, and impactful trials across the phases. Our expertise ranges from experimental medicine early phase studies exploring biological efficacy to trials which may deliver widespread change to routine practice, underpinned by applied methodology to drive forward clinical trial innovation. See our clinical trials Joining as a group leader, you will be given outstanding support to help you to continue to develop in your career. Along with a start-up package of funding, you will also have access to resources to establish your group, including support for recruiting key group members, such as PhD students and postdoctoral researchers. 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 Professor Emma Hall ([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

15/07/25

Thousands of women who undergo radiotherapy for low-risk breast cancer could be spared some of the side effects of treatment after a study confirmed that more targeted treatments are just as effective at controlling the disease in the long term.

Findings of the IMPORT LOW trial, which was led by The Institute of Cancer Research, London, and the University of Cambridge, have shown that limiting radiation to only the tumour area is just as effective as treating the whole breast, therefore reducing radiation exposure.

At the 10-year follow-up mark, the team showed that recurrence rates for the less aggressive technique – known as partial breast radiotherapy – were 3 per cent, the same as for whole breast radiotherapy, according to findings published recently in The Lancet Oncology.

Reducing long term side effects

Partial breast radiotherapy, which has been shown to reduce long-term changes in breast appearance, has now been adopted widely across the NHS and internationally.

It is hoped that more than 9,000 women a year in the UK – one in four patients who require radiotherapy for breast cancer – will benefit from the more personalised treatment, along with many tens of thousands of patients around the world.

More than 37,000 women have radiotherapy for breast cancer in the UK each year. The procedure is given after a tumour is surgically removed and is aimed at eradicating all remaining cancer cells.

Side effects of radiotherapy include changes in breast size or shape, swelling in the arm or breast due to fluid build-up, as well as pain or breast hardness.

Comparing three different approaches

The IMPORT LOW trial, which was managed by the Clinical Trials and Statistics Unit at The Institute of Cancer Research (ICR) and funded by Cancer Research UK, compared three radiotherapy approaches: whole-breast radiotherapy, partial-breast radiotherapy and partial-breast radiotherapy with reduced-dose to the part of the breast that was distant from the primary cancer. It involved more than 2,000 women at 30 radiotherapy centres in the UK who were monitored for 10 years after treatment.

Professor Judith Bliss, Founding Director of the ICR-CTSU, co-led the trial with Professor Charlotte Coles, from the Cambridge University Hospitals NHS Foundation Trust, who is the Chief Investigator. Professor John Yarnold at the ICR was the previous Chief Investigator between 2008 and 2013. The study was supported by the National Institute for Health and Care Research's Biomedical Research Centres in Cambridge and at The Royal Marsden and the ICR.

The researchers found no difference in rates of cancer recurrence with either of the less aggressive approaches, and patients reported significantly lower side-effects.

One in four patients will be eligible

Patients who received partial-breast radiotherapy were significantly less likely to experience long-term changes in breast appearance. Only 15 per cent of patients reported noticeable changes at five years, compared to 27 per cent in the whole-breast group.

Experts estimate that between 25-30 per cent of patients who have radiotherapy treatment for breast cancer are eligible for partial breast radiotherapy, due to their cancer being low risk and, to date, around 74,000 women have benefited from the gentler technique.

Following the trial's success, partial-breast radiotherapy has been integrated into NHS treatment guidelines and endorsed by the Royal College of Radiologists and Association of Breast Surgery. The IMPORT LOW trial has also changed clinical practice worldwide, informing the 2022 European Society of Radiation Oncology guidelines, and 2023 American Society of Radiotherapy and Oncology (ASTRO) partial breast irradiation guidelines.

Cost savings for the NHS

 Since 2020, partial breast radiotherapy has been carried out in five sessions of radiotherapy instead of 15 – making it cheaper for the NHS and less burdensome for patients.

Professor Charlotte Coles, Professor of Breast Cancer Clinical Oncology at the University of Cambridge, Honorary Clinical Oncology Consultant at Cambridge University Hospitals NHS Foundation Trust, and Chief Investigator of the IMPORT LOW study, said:

"The IMPORT LOW trial has transformed how we treat early breast cancer, offering women a safer and effective option while significantly reducing some side effects. By targeting the area around the tumour, rather than the whole breast, we have demonstrated that patients can achieve the same outstanding long-term outcomes with fewer complications. This approach is now widely adopted across the NHS, sparing thousands of women from unnecessary radiation exposure. The results of this study have not only shaped UK clinical practice but also informed international guidelines, ensuring that women worldwide benefit from this personalised, evidence-based treatment.”

First author Dr Anna Kirby, consultant clinical oncologist at The Royal Marsden NHS Foundation Trust and Reader in Breast Cancer Radiotherapy at The Institute of Cancer Research, London, said:

"The long-term results of this study confirm that a less aggressive approach - limiting radiotherapy to the part of the breast where the tumour was – is just as effective as traditional whole-breast radiotherapy. Patients receiving partial breast radiotherapy experience fewer side effects while maintaining excellent cancer control. This approach has now been widely adopted across the UK and internationally, significantly reducing the treatment burden while delivering the same long-term success."

Dr Fay Cafferty, Lead Statistician at The Institute of Cancer Research, London, and a co-author of the study, said:

"The 10-year findings from the IMPORT LOW trial are crucial in reinforcing the long-term safety and effectiveness of partial breast radiotherapy for women with early breast cancer. Long-term data is vital to ensure we know there's no greater risk of breast cancer returning after this targeted radiotherapy treatment. This latest analysis confirms that partial breast radiotherapy remains a safe and effective treatment option, supporting its continued adoption as the standard of care in the UK and globally. Along with the parallel reduction in the number of radiotherapy sessions now required, the approach provides significant advantages both for patients and healthcare systems, helping to optimise resources while ensuring excellent long-term cancer control."

Dr Dani Edmunds, Research Information Manager at Cancer Research UK, said:

"This study shows that we can safely reduce the amount of radiotherapy we give to many women with early breast cancer without increasing the risk of the disease coming back. This means people experience fewer long-term side effects, like changes in how their breasts look or feel, making the treatment kinder.

"At Cancer Research UK, we’ve been investigating the use of radiotherapy in cancer medicine for more than 100 years, but it’s far from old-fashioned. This work shows how research is continuing to refine, improve and innovate the treatment so people can live longer, better lives.” 

"Ten years on, I am doing fine...I am very thankful to have received the lowest dose of radiotherapy"

Hilary Stobart, now 70, was diagnosed with ER-Positive breast cancer in December 2008 which revealed a two-centimetre tumour in her left breast.

Hilary Stobart smiling

 

Hilary, then aged 54, underwent wide local excision surgery and was then offered the chance to take part in the IMPORT-LOW trial. She was treated with partial breast radiotherapy as part of the trial. She says:

“I had three weeks of radiotherapy, but suffered no side effects, other than some soreness in my breast and nipple in the first few weeks.

“Ten years on, I am doing fine. I have no side effects and no recurrence of disease. For me personally, I am very thankful to have received the lowest dose of radiotherapy. Whilst I may have had some niggling worries in the early days, having seen the results of the trial, I feel positive and optimistic now. I know that I was lucky enough back then to have had the best treatment, a treatment that other women will be routinely offered now.

“I am excited to have been part of a trial that has made a noticeable difference to the way in which breast cancer patients are treated now and in the future.”