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]

Location: Sutton

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Phone: +44 20 3437 3617

Email: [email protected]

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]

Location: Sutton

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Email: [email protected]

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Email: [email protected]

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Phone: +44 20 8722 4527

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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Phone: +44 20 3437 6358

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Phone: +44 20 3437 6131

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 1/2025

See all their publications

Vacancies in this group

Working in this group

Postdoctoral Training Fellow - Endocrine Control Mechanisms

  • Chelsea
  • Endocrine Control Mechanisms
  • Salary Range: £45,600 - £55,000 per annum
  • Fixed term

Under the guidance of Professor Cathrin Brisken, we are seeking a highly motivated and ambitious Postdoctoral Training Fellow to combine innovative patient-derived xenograft models and genetic tools to disentangle the role of estrogen and progesterone receptor signaling in breast cancer. The work contributes to gaining more insights into patient-specific hormone dependencies and factors determining them with the aim of personalizing breast cancer therapy and prevention. The successful candidate will be part of a transdisciplinary team of biologists, clinicians and computational scientists and part of close interactions with groups at the ICR, the RMH and King’s College as well Prof. Brisken’s research group at EPFL, Switzerland. About you The successful candidate must have a PhD in biochemistry, pharmacology, cell or molecular biology and demonstrable experience in planning and designing experiments. Ability to write efficient computer code would is desirable. Candidates who are nearing completion of their PhD may apply, but confirmation on awarded PhD is required within 6 months of employment. The ICR has a workforce agreement stating that Postdoctoral Training Fellows can only be employed for up to 7 years as a PTDF at the ICR ( this includes experience gained at PDTF level prior to joining the ICR). For general information on Postdocs at The ICR, more information can be found here. Research Group Information Under the leadership of Professor Cathrin Brisken, The Endocrine Control Mechanisms group are using intraductal mammary gland implantation, and ex vivo studies using breast cancers expanded via intraductal implantation. We also use transcriptomic and proteomic studies to investigate therapeutics for breast cancer patients and improve the development of novel treatment options for them. Directorate Information The Breast Cancer Now Toby Robins Research Centre, within the Division of Breast Cancer Research of the Institute of Cancer Research which is the first centre in the UK entirely devoted to breast cancer research. Our goal is to advance research into the causes, diagnosis and treatment of breast cancer. It is located in state-of-the-art laboratory space, with excellent core facilities and is funded through a long term renewable programme grant from Breast Cancer Now. The Centre is Directed by Clinician Scientist Professor Andrew Tutt, Professor Chris Lord is Deputy Director of the Centre. 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.

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]

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

03/04/25 - by

By Charles J. Sharp - Own work, from Sharp Photography, sharpphotography.co.uk, CC BY-SA 4.0, https://commons.wikimedia.org/w/index.php?curid=143473295

Image: QBiotics' scientists isolated tiglanol tiglate after observations that the musky rat-kangaroo (pictured) found the seeds of the blushwood tree unpalatable. Credit Charles J Sharp, sharpphotography.co.uk, CC BY-SA 4.0

Scientists at The Institute of Cancer Research, London, are collaborating with life sciences company QBiotics to unravel the molecular and cellular mechanisms of a potential new cancer drug.

The collaborative team will study the effects of tigilanol tiglate – a naturally occurring small molecule derived from the seeds of the blushwood tree, Fontainea picrosperma, which grows in the rainforests of northeastern Australia.

They are investigating its effects in samples from patients with head and neck cancer taking part in a clinical trial.

Injected directly into tumours, this potential new drug is currently under development as a treatment for a range of solid tumours, including head and neck cancer and soft tissue sarcoma.

The blushwood tree has long been of interest to QBiotics’ scientists after they observed that animals that feed on its fruit, such as the musky rat-kangaroo – the world’s smallest kangaroo – find the seeds highly unpalatable.

The tree likely evolved this trait to protect the seeds during dispersal across the jungle floor.

QBiotics’ chemists subsequently isolated a compound with anti-cancer properties from the seed – tiglanol tiglate – which may also be responsible for its unpalatability and developed a method for semi-synthesising it in the laboratory. Tigilanol tiglate is already registered in the UK, Europe, the USA and Australia for use as a cancer treatment for dogs and is under development as a cancer treatment for humans.

Studies by QBiotics show that tigilanol tiglate has a multifactorial mode of action, directly destroying treated tumour cells, disrupting the tumour blood supply, triggering a localised immune response and potentially leading to a systemic immune response in some patients. However, the drugs precise mechanism of action remains unclear.

Translational research

The Institute of Cancer Research (ICR) team involved in the study is based in the Centre for Immunotherapy of Cancer, a joint initiative between the ICR and our hospital partner The Royal Marsden NHS Foundation Trust.

The Centre aims to increase communication between clinicians and scientists with an interest in translational immunotherapy and is seeking further collaborations with industry in innovative research.

A phase II clinical trial, led by QBiotics, is currently underway to assess the effectiveness of tigilanol tiglate for the treatment of patients with advanced head and neck cancer.

In this study, the ICR and Royal Marsden researchers will analyse blood and tumour samples collected from the participants before and after treatment with tigilanol tiglate. The results will provide valuable insights into the drug’s mechanism of action, particularly its effects on the body’s immune response.

In addition to its potential as a monotherapy, preclinical studies suggest that tigilanol tiglate could enhance the effectiveness of other cancer treatments, including immunotherapy, chemotherapy and radiotherapy.

Gaining a better understanding of the drug’s mechanism of action could lead to the development of combination strategies that are even more powerful at destroying solid tumours.

Dr Antonio Rullan, honorary postdoctoral research fellow at the ICR and Clinical Research Fellow at University College London, said:

“We’re very pleased to be working with QBiotics to uncover new insights into how tigilanol tiglate exerts its effects on tumours and the immune system in people. Interestingly, this is a natural compound initially derived from the North Australian blushwood tree. Ultimately, we hope these findings accelerate the development of a much-needed new treatment option for patients with head and neck cancer worldwide.”

Dr Steven Ogbourne, Chief Translational Research Officer at QBiotics, said:

“This collaboration represents an important aspect of exploring tigilanol tiglate’s potential as a cancer treatment. By leveraging the ICR’s cutting-edge technology and world-class expertise in translational research, we hope to deepen our understanding of the precise mechanism of action of this promising drug candidate.

“Ultimately, the findings could help us navigate towards the most effective way of using tigilanol tiglate to deliver significant benefits for patients with a range of solid tumours.”

Jennifer Hodgson, Business Development Manager at the ICR, said:

“We’re delighted to be working in collaboration with QBiotics on this fascinating investigation of tiglanol tiglate, which is using the expertise of scientists in our Centre for Immunotherapy of Cancer to help to elucidate its mechanism of action. It’s a great example of a team from academia and industry combining to answer questions that might not be possible to answer alone, and which could end up having a big impact on patients in the future.”