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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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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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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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]

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

Senior Technician - in vivo biology

  • Sutton
  • Research Services
  • Permanent

About you The ICR is one of the world's leading cancer research institutes, aiming to defeat cancer. As a Senior Laboratory Technician you will contribute directly to this mission by supporting vital in vivo research. We are looking for a highly motivated, detail-oriented individual, committed to high-quality work. Key requirements include: Education and Knowledge BSc in Life Sciences or IAT Level 3 (Essential) Home Office Personal Licence (PILA, B, C) or equivalent (Essential) Understanding of tumour biology and pre-clinical models (Desirable) Skills Skilled in dissection, surgery, dosing of agents and sampling techniques (Essential) Strong organisational, communication and interpersonal skills (Essential) Ability to work independently and in a team with other scientists and BSU staff (Essential) Computer proficiency and willingness to pursue professional development (Essential) Experience Proven experience in in vivo oncology and PDX models (Essential) Strong foundation in animal (rodent) husbandry and behaviour (Essential) Experience in stereotaxic surgery, imaging techniques and sample preparation (Desirable) 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 Department/Directorate Information 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 Bishani Wickrama via email on: [email protected].

Business Development Manager

  • Sutton
  • Business & Innovation Office
  • £61,275 - £74,175
  • Permanent

About the Role We are seeking a Business Development Manager to join The Institute of Cancer Research’s (ICR’s) Business and Innovation Office and contribute to to support a portfolio of academics by protecting and commercialising their research, supporting them in securing translational funding and to highlight to them the benefits of working with industry. The successful candidate will play a key role in strategic project evaluation, stakeholder engagement, IP protection, commercial deal-making (collaborations and licensing), and translational funding support. Key Responsibilities Identify and assess commercially viable research Protect IP and manage confidentiality agreements Draft and negotiate licensing and collaboration contracts Support translational funding applications Drive spinout opportunity management About You We are looking for a proactive, detail-oriented team player. PhD, MBA or equivalent in a relevant field Experience in business development or technology transfer Direct experience of negotiating and closing deals with external partners Strong communication, negotiation, and organizational skills What We Offer • Supportive, collaborative environment • Career development opportunities • Competitive salary and pension Department/Directorate Information The Business and Innovation Office drives commercialisation and strategic partnerships to maximise patient benefit. For more details, please refer to the job pack. For an informal discussion regarding the role, please contact Dr. Amritha Nair via Email on [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

17/10/25

Giving patients with suspected bladder cancer an MRI scan before surgery could mean they would be treated more quickly, leading to fewer deaths due to the disease, new research suggests.

Researchers from the  University of Birmingham  and The Institute of Cancer Research, London presented the results of the BladderPath trial today at the ESMO Congress 2025 in Berlin.

Fewer delays in diagnosis

 The findings, funded by the National Institute for Health and Care Research, show that adding an initial MRI for patients with possible muscle-invasive bladder cancer (MIBC) prior to a usual procedure led to fewer delays in diagnosis (42 per cent among those receiving MRI first vs 54 per cent on standard pathway) and fewer bladder cancer specific deaths (10 per cent on MRI pathway vs 18 per cent on the standard pathway). 

 The BladderPath trial was a multistage randomised controlled trial across 15 sites in the UK that recruited 143 participants newly presenting with a bladder mass following initial exploratory diagnosis. Participants were randomised to either enter the standard pathway, in which they would go onto a waiting list for transurethral resection of bladder tumour (TURBT), or the experimental pathway which added multiparametric MRI prior to TURBT. 

‘Not only can we cut the time taken to receive treatment – we can cut bladder cancer deaths’

Professor Nick James from The Institute of Cancer Research, London and chief investigator of the BladderPath trial said: 

“This research shows that by adding an MRI pre-biopsy, not only can we cut the time taken to receive treatment – but importantly, we can cut deaths due to bladder cancer.  

 “An MRI is considerably cheaper than the surgical bladder tumour resection (TURBT) and the pre-surgery imaging allows some patients to either avoid surgery altogether or have a more limited procedure. We estimate that this new diagnostic pathway will save money, save surgical theatre space and hospital bed days, and prevent patients from undergoing unnecessary procedures. We’re now pleased to say that this research shows that the pathway will also save lives, and I hope that it will be put into practice immediately." 

 ‘This simple change to the patient pathway saves lives’

Professor Richard Bryan from the University of Birmingham  and one of the investigators of the BladderPath trial said: “Previous studies have shown that adding MRI to the existing pathway for bladder cancer diagnosis can vastly speed up time to definitive treatment which is crucial. The bladder cancer diagnostic pathway has remained essentially unchanged for more than 30 years while the rest of medicine and healthcare has innovated around it. 

“These latest results show that new approaches can make a significant difference. Our data confirms that changes to the usual diagnostic pathway could have a significant impact for patients, not only speeding up time to correct diagnosis and treatment, but also reducing failure events and increasing the odds of surviving bladder cancer. 

“This simple change to the patient pathway saves lives. There is no reason for it not to be adopted and implemented immediately."