Completed Cancer Lungs & Breathing

ICF: Novel smant of CCNE1-amplll molecule inhibitors for the treatmeified cancers

In plain English

AI plain-English summary

One in five patients with high-grade serous ovarian cancer carry tumour cells that are addicted to a single protein, cyclin E, and this project aims to develop a drug that kills those cells while sparing healthy tissue. Patients with this aggressive cancer currently face harsh chemotherapy that offers little improvement to either the length or quality of their lives. The cancer’s vulnerability stems from multiple copies of the cyclin E gene, which flood the cell with the protein and make it essential for the tumour’s survival. The team has already identified chemical starting points and used structural studies to understand how to block the aberrant cyclin E signal with a small molecule inhibitor. If successful, this work would produce a prototype inhibitor that selectively destroys ovarian cancer cells with elevated cyclin E, while leaving other cells unharmed. Clinicians could identify eligible patients through a simple genetic test, making this a personalised medicine approach. The project aims to advance the inhibitors to a stage where they show clear selective effects, positioning them for final optimisation toward a clinical drug.

View original technical description
This project aims to take important steps towards developing a drug that will target the Achilles' heel of the cancerous cells found in 1 in 5 patients diagnosed with high grade serous ovarian cancer. Patients with this form of cancer currently have a very poor prognosis, and undergo harsh chemotherapy that provides limited benefits in terms of quality or duration of life. The vulnerability of the ovarian cancer in these patients arises from the fact that these particular cancer cells have multiple copies of the gene that encodes cyclin E. This results in cyclin E protein being produced at abnormally high levels and as a consequence the cells become addicted to cyclin E for their ability to further divide and survive. Our structural studies have provided novel insights into how aberrant cyclin E signaling may be prevented with a small molecule inhibitor, which would be selectively toxic to ovarian cancers that are dependent upon this pathway for survival. The project team has extensive expertise in drug discovery and has established the experimental systems needed to develop such inhibitors, with chemical start points being identified. The team has also formed collaborations with clinical experts who specialise in the treatment of aggressive ovarian cancers. Clinicians would be able to easily identify the patients with elevated cyclin E who would benefit from a drug developed for these tumour cells; an example of a personalised medicine. By the end of the project, the team aims to have developed the inhibitors to a point where they can demonstrate selective effects on ovarian cancer cells with elevated cyclin E levels. This would position the project for further development involving the final optimisation of inhibitors towards a drug that could be developed for clinical use.

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Researchers

Celine Cano (Co-Investigator)Jane Endicott (Co-Investigator)Martin Noble (Co-Investigator)Michael Waring (Co-Investigator)Steve Wedge (Principal Investigator)

Related Research

Grants with similar aims, by meaning.

Novel small molecule inhibitors for the treatment of CCNE1-amplified cancers.
Therapeutic targeting for ovarian cancer
Targeting ovarian cancer using fragment-based drug discovery
Novel approaches to enhance anti-mitotic chemotherapy
Project 50.1: Targeting pancreatic cancer invasion with novel therapeutics

Original classification

Research Grant

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