Centre for In Vivo Modelling Service Core

At the Centre for In Vivo Modelling (CIVM), we combine advanced animal genetics and cutting-edge technologies to drive cancer research. Our multidisciplinary team specialises in the generation and maintenance of genetically engineered mouse models (GEMMs), humanised mouse strains, and patient-derived models (xenografts and organoids), using innovations such as CRISPR gene editing, embryo manipulation, and in vivo genetic screening. We develop and cryopreserve new cancer models that closely replicate human disease, supporting translational studies that inform effective therapies. Our approach integrates rigorous scientific standards, ethical oversight, and collaborative expertise, aiming to accelerate progress in understanding cancer biology and developing better treatments for patients.

Our Centre is dedicated to driving innovation and excellence in cancer research through advanced in vivo modelling. We work in close collaboration with the ICR researchers and clinicians at The Royal Marsden to generate genetically engineered mouse models (GEMMs) and patient-derived models, such as patient-derived xenografts (PDXs) and patient-derived organoids (PDOs) to interrogate cancer biology in its own ecosystem. By leveraging these sophisticated in vivo systems, the Centre aims to:

  • Develop innovative cancer models in collaboration with ICR researchers to advance cancer research and drug discovery.
  • Work in partnership with The Royal Marsden Hospital to obtain patient samples and generate new patient-derived cancer models for translational studies.
  • Foster close interdisciplinary collaboration with drug discovery teams to leverage these in vivo models in the creation and testing of next-generation anti-cancer therapies.
  • Continuously improve the sophistication and relevance of our cancer models, ensuring they more faithfully recapitulate the complexity of human disease and enhance the translational impact of our research.

 

Our services

Advantages of cryopreserving your strains:

  • Allows you to save space, by getting the mice you need, when you need;
  • Reduces your animal costs;
  • Reduces animal use;
  • Reduces risk from disasters (e.g. disease outbreaks, breeding cessation, equipment failures, genetic contamination, natural disasters, etc…).

 What can be cryopreserved?

  • Mouse Sperm
  • Mouse Embryos
  • Mouse Embryonic Stem Cells
  • Mouse Oocytes

 Sperm Cryopreservation:

Description: Sperm is retrieved from the epididymal tissues of 3 male mice and is cryopreserved in 20 to 30 straws that are stored in liquid-phase, liquid nitrogen across two tanks in two separate locations (SRD and CCDD), to ensure sample safety and mitigate risks associated to unexpected or uncontrollable events.

Material needed: 3 males, reproductively active, 12-25 weeks old

Timeline: 2-6 weeks (dependant on QC method of choice)

Considerations: this method of cryopreservation is rapid and cheap; however, it only preserves half of the genome. This method is only recommended for single mutations on a common inbred background.

Quality Control: we provide different levels of Quality Control (QC) for different price ranges.

  1. Test thaw QC: we will thaw 1 straw the day after cryopreservation and visually assess motility and viability of the recovered sperm
  2. IVF and culture to blastocyst QC: we highly recommend this QC step. In addition to test thaw, we will also perform IVF and culture embryos up to blastocyst stage. We will provide the investigator with a fertility rate (%) for the recovered sperm. We will charge an extra cost to cover the IVF procedure.
  3. IVF and embryo transfer QC: In addition to test thaw, we will perform IVF and transfer 2-cell embryos into up to 3 pseudopregnant females to generate viable embryos/live pups. We will charge an extra cost to cover the IVF and embryo transfer procedures.

    Please note that we require you to provide your genotyping protocol, as well as full detail of the genetic content of each strain that you submit for cryopreservation.

Diagram of Sperm Cryopreservation

Embryo Cryopreservation:

Description: Female mice are hormonally superovulated and oocytes are retrieved for in vitro fertilisation (IVF) with sperm from donor male. Resulting embryos are placed in cryoprotectant and loaded into multiple straws, which are gradually cooled and stored in liquid-phase liquid nitrogen in two separate tanks.

Material needed: Donor male and 8-10 donor females

Timeline: 12-15 weeks

Diagram of Embryo Cryopreservation

Embryonic Stem Cells Cryopreservation:

Not available, yet.

Oocyte Cryopreservation:

Not available, yet.

Cryostorage:

If you have cryopreserved mouse sperm/embryo/oocytes at another institution, we can cryostorage your samples for an annual fee. We do require that the investigator takes charge of shipping costs into our facility, and that thawing and genotyping protocols are submitted to the CIVM.

The CIVM stores all samples in liquid-phase liquid nitrogen tanks (CryoPlus1, ThermoFisher Scientific). Material retrieved from each strain is split between 2 tanks, a main and a backup tank, for redundancy. For additional safety, these 2 tanks are located in two separate buildings at ICR Sutton. Both tanks are continuously monitored by T-scan alarm systems and undergo annual service, as well as daily visual inspections.


 

Sperm Cryorecovery:

Description: Frozen sperm is cryorecovered by IVF, followed by embryo transfer. We can purchase wild-type female oocyte donors of the same genetic background, or alternatively the investigator can provide homozygous oocyte donors of the same strain.

Material needed: straw with frozen sperm and 8 to 12 females for IVF, 7-16 weeks old.

Timeline: 12-15 weeks

Diagram of Sperm Cryorecovery

 

Embryo Cryorecovery:

Description: Frozen 2-cell embryos are thawed and transferred into pseudopregnant females.

Material needed: straw(s) with frozen 2-cell embryos

Timeline: 8-10 week


Oocyte Cryorecovery:

Not available, yet.

 

Mouse rederivation

Description: Mouse rederivation is a process used to produce pathogen-free mouse colonies by removing microbial contaminants from existing lines. The procedure can be performed either through natural mating or in vitro fertilization (IVF):

  • In natural mating, embryos are obtained from donor mice and transferred into pathogen-free recipient females.
  • In IVF-based rederivation, fertilized embryos are created in vitro using gametes from donor mice and then implanted into clean recipient females.

Both methods effectively eliminate pathogens, allowing safe importation of mouse strains from lower health-status facilities into the ICR BSU. Samples from both litter and recipient mother will be sent for Health Screening and the associated costs will be charged separately to the Investigator.

Material needed: For IVF-based rederivation we require the investigator to provide 2 males, reproductively active, 12-25 weeks old, and the CIVM will purchase wild-type female egg-donors. Alternatively, if maintaining homozygosity is essential, the investigator will need to provide additional 6-10 females, 7-16 weeks old.

Timeline: 12-15 week

Mouse Rederivation Mating Diagram

Mouse Rederivation IVF diagram

We are currently setting up CRISPR/Cas9-based gene editing protocols. Soon, you’ll be able to apply for projects that involve developing new alleles based on:

  • Knockout by indel formation
  • Knockout by precise deletion
  • Conditional knockout
  • Knock-in of point mutations
  • Knock-in of small tags
  • Large knock-in
  • Exon replacement

These alleles will be developed based on Electroporation of Microinjection of CRISPR/Cas9 system reagents.

We will collaborate with you to design the best strategy and help you generate the genetically engineered mice you need for your project. 

We also provide:

  • Development of humanised mouse strains
  • Development of Patient-derived xenografts (PDX) and organoid models

Latest ICR News

25/04/26

DNA Day marks the anniversary of two important events in the history of genetics – the publication of the discovery of the DNA double helix in 1953, and the completion of the Human Genome Project in 2003. It is celebrated every year on April 25 to champion the remarkable scientific discoveries made possible by genetic research, and highlight the ongoing impact of genetics in science and medicine.

At The Institute of Cancer Research (ICR), genetic research is a fundamental part of what we do. Understanding the role DNA plays in why cancer develops and spreads is essential to advance research and accelerate discoveries for patients.

What is DNA?

DNA (deoxyribonucleic acid) is a molecule inside our cells that carries genetic instructions for how the body is built and functions. It works like a biological instruction manual, telling cells how to grow, divide and repair.

DNA Helix

DNA - the cornerstone of cancer research

Understanding DNA is the cornerstone of cancer research. DNA controls how cells grow and divide, but if DNA is damaged or copied incorrectly, it can lead to harmful changes. These changes can drive diseases such as cancer, which is why genetic research is vital for prevention, diagnosis and treatment. Understanding the genetic make-up of cancer is also crucial for providing more targeted treatments and improving outcomes for patients.

A long track record of success

The ICR has been at the forefront of genetic research for decades. ICR scientists were the first to make the link between DNA damage and cancer, paving the way for the now universally accepted idea that cancer is a genetic disease.

And it was our researchers who discovered the BRCA2 breast, ovarian, pancreatic and prostate cancer gene, helping people with the genetic mutation make informed decisions to reduce their cancer risk.

Today, our scientists are still leading the way in cancer genetics. Building on our long history of breakthroughs, we continue to make significant strides in the lab, driving research that that will lead to innovative new therapies and bring hope for people with cancer.

Read about three of our recent pioneering DNA discoveries below.

Map of DNA changes improves treatment options

ICR scientists helped build the most detailed map to date of the DNA changes that fuel cancer development – opening the door to extending precision treatments to thousands more patients. They analysed data from nearly 11,000 cancer patients in Genomics England’s 100,000 Genomes Project, looking at millions of mutations across 16 different cancer types. This identified 134 distinct “mutational signatures” – patterns of DNA damage that reveal the processes that drive cancer’s development – including 26 signatures not seen before.

One of the most significant discoveries was the high number of cancers showing signs of homologous recombination deficiency (HRD) – a DNA repair weakness that makes tumours particularly vulnerable to PARP inhibitors and platinum‑based chemotherapy.

1950s tumour samples could solve modern cancer mystery

Preserved tumour samples from the 1950s and 60s could help reveal why bowel cancer cases are rising in the under-50s. In the Boomers Project, ICR researchers will study the DNA of tens of thousands of tumour samples dating back decades, and compare it to the DNA of cancers diagnosed today.

Different environmental exposures, such as smoking or diet, can leave distinctive patterns of DNA damage in tumours. The researchers plan to use genome sequencing techniques – including novel approaches developed at the ICR – to map how the DNA is altered in the cancer specimens from the 1950s compared to cases from the present day. By analysing what has changed over the decades, the team hopes to identify clues to the environmental and biological factors driving the rise in early-onset disease. In time, this could inform future strategies for prevention, earlier diagnosis and more tailored treatment.

Our research is giving everyone with bowel cancer the hope of a cure and, potentially, preventing the disease from developing in the first place. Give a regular gift today to help us make more discoveries and save more lives.

Make a regular gift

DNA repair research could improve existing cancer treatments

Our DNA is continually being damaged, and cells rely on specialised repair mechanisms to fix it. ICR researchers have uncovered how a key DNA repair enzyme is recruited and activated inside cells, answering long-standing questions about how cells protect and repair DNA, and providing the structural groundwork that could help improve existing cancer treatments.

DNA repair pathways are essential for normal cells, but they can be exploited by cancer cells for survival and growth. Our researchers plan to use AI to explore how to disrupt or enhance certain connections between repair enzymes. With further research, this could help scientists discover how to manipulate DNA repair in cancer cells, preventing them from dividing and spreading.

Celebrating the science that is defeating cancer

From decoding DNA damage to uncovering how DNA repairs itself, and even learning from decades-old tumour DNA, our genetic research continues to shape how we understand and treat cancer.

This DNA Day, we’re celebrating the science that made these breakthroughs possible, and the progress that is still to come.