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

28/11/25

Experts at The Institute of Cancer Research, London, have responded to the draft recommendation from the National Screening Committee (NSC) to implement a targeted prostate cancer screening programme for men with a confirmed BRCA1 and BRCA2 variant.

The draft recommendation, which will now go to a public consultation for three months, has recommended that men with a confirmed BRCA1 and BRCA2 variant should have a PSA test every two years, from age 45 to age 61.

Vital step towards reducing deaths

Professor Ros Eeles, Professor of Oncogenetics at The Institute of Cancer Research, London, said the move would represent a vital step towards reducing deaths from prostate cancer:

"We're very pleased to see that the National Screening Committee has recommended that PSA testing for men who carry BRCA1 and BRCA2 mutations is introduced. This recommendation is based on research led by my team at The Institute of Cancer Research, which showed that these men face a significantly higher risk of developing prostate cancer and are more likely to experience aggressive forms of the disease. PSA testing picks up cancers at an earlier stage, when they are easier to treat – which will ultimately save lives."

However, Professor Eeles added that cancers could be missed if screening only occurs every two years. Data from the IMPACT screening trial showed that cancers were picked up in each year that BRCA2 carriers were tested, and in all but one of the five consecutive years that BRCA1 carriers were tested.

Professor Eeles added:

"We therefore recommend annual screening, rather than every two years – to avoid the risk that an aggressive cancer could be allowed to grow unchecked for a whole year.

"The NSC has recommended that BRCA carriers be tested from the age of 45 to 61. Our research offered screening for cancers for a wider age range, and I am concerned that if you stop screening at 61 years of age, a large number of cancers will be missed. Of the cancers we found in the IMPACT trial, 49 per cent of them in BRCA1 carriers were between the ages of 61-69, and for BRCA2 carriers 42 per cent were in this age group. We are urging regulatory bodies to act on the evidence, offering all men with a BRCA1 or BRCA2 mutation from the age of 40 – up until the age of 69 – annual PSA testing. This has been the recommendation in Europe, to date, for BRCA2 carriers.

"Today’s recommendation is indeed a vital step toward reducing deaths from prostate cancer. However, unless BRCA testing is expanded, there are thousands of men who will miss out on this screening programme. The NHS needs to offer BRCA testing to more men, starting by offering testing to male relatives of BRCA carriers."

Discovering the BRCA2 gene

The Institute of Cancer Research (ICR) has played a pivotal role in providing the evidence for today’s decision.

It was 30 years ago this year that researchers at the ICR discovered the BRCA2 gene, which plays an essential role in protecting against cancer. Inherited faults in this gene, and in BRCA1, can significantly increase the risk of breast, ovarian, prostate and pancreatic cancers.

BRCA carriers are at greater risk of prostate cancer

ICR researchers led the IMPACT trial which, in 2019, reported findings that annual PSA testing picked up prostate cancers more often, at a younger age and in more dangerous forms in men with BRCA2 mutations than in non-carriers. The team have been calling for regular PSA testing for these men from the age of 40, ever since.

This year, results from the trial showed that men with BRCA1 mutations should also be offered an annual PSA test. These men are more than three times as likely, compared with non-carriers, to have aggressive prostate cancers that are likely to grow and spread quickly.

Expanding access to BRCA testing

While the decision to screen BRCA carriers for prostate cancer is a vital step toward ensuring that those at greatest risk receive the earliest interventions, there are currently thousands of men who will not know they have a BRCA variant.

There are up to 32,000 men in the UK aged 45-69 who could have the BRCA variant, but testing to date has focused on women, where the evidence around higher cancer risk and mitigations have been clearer for decades.

The NHS needs to expand BRCA testing, and the ICR has been leading the way at improving capacity. The ICR’s BRCA-DIRECT study trialled an innovative patient-centred digital pathway, to reduce the turnaround time for results. Using a new online platform, participants could access their pre-test information, give consent, provide a saliva sample and receive their results in their own time.

Professor Clare Turnbull, Professor of Translational Cancer Genetics at The Institute of Cancer Research, London, said:

"Individuals can only access a BRCA test via the NHS if eligible based on their personal or family history of cancers, as per the Genomic Medicine Service National Test Directory. Only individuals who have had ovarian cancer or particular forms of breast, prostate or pancreatic cancer are eligible, or those who are unaffected but have a close, strong family history of these cancers."

Leading trials to identify markers for other high-risk groups

Black men are also at an increased risk of developing prostate cancer. The NSC has not recommended screening for this group, as they state that there is currently a lack of data.

Researchers at the ICR have identified new genetic variants that could explain some of this increased risk and have built a genetic profile of prostate cancer risk that is applicable to men of diverse ancestries.

At the moment, the PSA test is not a good enough marker of increased risk of disease in this group of men, as they have a naturally higher PSA level than men of European ancestry.

The ICR is leading the PROFILE trial, which is carrying out targeted screening for Black men, men with a family history of prostate cancer, and those with genetic alterations including BRCA. Recruitment is still open for the study, and if you fit into one of these groups, the researchers are inviting people to sign up. The study involves MRI scans, a biopsy and biological samples, to look for new markers that we hope will be better at detecting prostate cancer than a PSA test.

In addition, the ICR is a co-lead on the TRANSFORM trial – the biggest prostate cancer screening study in a generation. The trial will test the most promising prostate cancer screening techniques available – including a saliva test to assess genetic risk of the disease – to identify the safest, most accurate and most cost-effective way to screen men. The TRANSFORM trial will ensure that at least 1 in 10 men invited to take part are Black, in order to build an evidence base for the NSC to consider.

Professor Ros Eeles said:

"We know that Black men are also at a higher risk of developing prostate cancer. At the moment, the PSA test is not a good enough marker of increased risk of disease in this group of men. This is why we at the ICR are leading the PROFILE trial, to look for new markers that we hope will be better at detecting prostate cancer.

"We are also co-leading the TRANSFORM trial, which will compare different methods of detecting prostate cancer using MRI and genetics – and which aims to recruit more Black men than any previous trials, in order to build this evidence base. We’re looking forward to feeding into the consultation process in the coming months."

Read more about our prostate cancer research