Cellomatics Biosciences
Cellomatics Biosciences
Cellomatics Biosciences

Oncology

In Vitro Inflammation Models for Preclinical Drug Discovery

Developing new cancer therapies is complex, and generating reliable preclinical data is essential for making informed decisions at every stage of development. Cellomatics provides oncology CRO services that support biotech and pharmaceutical companies throughout the drug discovery process, from target validation and assay development to lead optimisation and candidate selection.

Our scientists work closely with clients to develop and deliver tailored oncology assays that address specific research objectives. By combining phenotypic screening, high-content imaging and translational tumour models, we help teams evaluate drug candidates more effectively and generate data that supports confident decision-making.

As a specialist cancer drug discovery CRO, we understand the challenges of balancing scientific rigour with development timelines and budget constraints. Our preclinical oncology research capabilities are designed to provide the expertise, technologies and insights needed to advance promising oncology programmes while reducing risk and avoiding unnecessary delays.

What are oncology CRO services?

Oncology CRO services help biotech and pharmaceutical companies progress cancer drug discovery projects by providing specialist research expertise and laboratory support. Rather than investing in new infrastructure or expanding internal teams, organisations can access the scientific capabilities they need through an experienced external partner.

A cancer drug discovery CRO typically supports activities such as assay development, compound screening, high-content imaging and preclinical studies. This allows research teams to generate robust data, answer critical scientific questions and keep programmes moving forward without overextending internal resources.

Many companies turn to oncology research services when they need additional expertise, faster turnaround times or access to specialised technologies. The goal is not simply to outsource experiments, but to work with a partner that understands the challenges of drug discovery and can help deliver the data needed to make confident development decisions.

Supporting cancer drug discovery

Successful drug discovery depends on making the right decisions at each stage of development. As a cancer drug discovery CRO, Cellomatics supports clients throughout this process, generating the data needed to evaluate opportunities, reduce risk and prioritise the most promising candidates.

Our scientists work with clients from target identification and target validation through to hit identification, lead optimisation and mechanism-of-action studies. At each stage, we design studies that address specific scientific questions, helping teams understand target biology, assess compound activity and build confidence in development decisions.

Through our cancer drug discovery services, clients gain access to specialist oncology expertise, advanced assay platforms and translational models that support informed decision-making. By generating robust, reproducible data early in development, our preclinical oncology research capabilities help teams focus resources on candidates with the greatest potential for success.

Oncology assay capabilities

Cancer drug discovery relies on using the right assay for the question being asked. No single model can capture every feature of tumour biology, which is why Cellomatics offers a broad portfolio of oncology assays to support different stages of preclinical research.

Our oncology CRO services include assays designed to investigate key cancer-related processes such as cell proliferation, apoptosis, DNA damage, migration, invasion and metastasis. These studies help clients understand how compounds behave in relevant cellular systems, whether they are assessing target engagement, comparing lead candidates or exploring mechanism of action.

By selecting the most appropriate assay format, readout and model system, our scientists help generate data that is practical, interpretable and aligned with the needs of each programme.

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Proliferation assays

Cancer cells are characterised by their ability to sustain uncontrolled growth and evade the normal mechanisms that regulate cell division. A cell proliferation assay measures changes in cell number over time, providing a direct assessment of treatment response and anti-cancer activity. Among the most widely used approaches, the BrdU proliferation assay and BrdU cell proliferation assay quantify DNA synthesis during cell division, helping researchers evaluate compound efficacy, compare candidate therapies and identify agents that inhibit tumour cell growth.

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Apoptosis assays

Apoptosis is a tightly regulated form of programmed cell death that removes damaged or unwanted cells. Many anti-cancer therapies work by triggering this process, making apoptosis an important indicator of treatment response. Apoptosis & viability assays help researchers determine whether a compound is killing cancer cells and provide insight into its mechanism of action. Common approaches include Annexin V staining to detect early apoptosis, CellTiter-Glo® viability testing to measure metabolically active cells, and complementary cell death assays and cell toxicity assays to assess overall treatment effects.

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DNA damage assays

DNA damage plays a central role in cancer development and is also a key mechanism of action for many oncology therapies. A DNA damage assay can be used to measure genotoxic effects, assess treatment response and investigate activation of DNA damage response pathways. Complementary DNA damage assays and DNA repair assay approaches help researchers understand how cells detect and repair genomic lesions, providing valuable insight into drug sensitivity, resistance mechanisms and the development of targeted cancer therapies.

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Senescence assays

Cellular senescence is a state of long-term growth arrest in which cells remain metabolically active but no longer divide. Many anti-cancer therapies induce senescence as a mechanism to suppress tumour growth, making it an important response to measure during drug development. A cellular senescence assay can be used to identify and quantify these changes, often through SA-β-gal staining and biomarker analysis. Combined with other endpoints, a senescence assay helps researchers evaluate treatment efficacy, mechanism of action and long-term cellular responses to therapy.

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Tumour progression & metastasis models

Cancer progression is rarely driven by tumour growth alone. As cancer cells adapt, they can invade surrounding tissue, enter the circulation and establish secondary tumours in distant organs. This metastatic spread is one of the main reasons cancer becomes harder to treat, making it a critical process to study during oncology drug development.

Modelling tumour spread helps researchers understand how potential therapies affect migration, invasion, survival and colonisation in more relevant systems. These studies can show whether a compound only slows cell growth or also interferes with the behaviours that enable metastasis. By building this evidence early, drug discovery teams can make better decisions about candidate selection, mechanism of action and the likelihood of meaningful anti-cancer activity.

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Adhesion assays

Cell adhesion plays an important role in how cancer cells interact with neighbouring cells and the surrounding extracellular matrix. Changes in these interactions can promote tumour progression, enabling cells to detach, migrate and invade new tissues. A cell adhesion assay helps researchers measure these behaviours and understand how potential therapies affect metastatic potential. Using cell adhesion assays and related adhesion assay formats, drug developers can investigate mechanisms of invasion and identify compounds that may limit cancer spread.

 

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Migration assays

Cell migration is a key step in tumour dissemination, allowing cancer cells to move away from the primary tumour and invade surrounding tissues. Understanding this behaviour is important when evaluating therapies designed to limit cancer spread. A migration assay measures the ability of cells to move in response to specific signals or treatments, providing insight into metastatic potential. Using cell migration assay platforms and other migration assays, researchers can assess whether candidate therapies reduce cell movement and support the development of anti-metastatic strategies.

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Invasion assays

For cancer cells to spread beyond the primary tumour, they must first penetrate surrounding tissues and extracellular barriers. An invasion assay is designed to measure this behaviour, providing insight into the mechanisms that drive metastatic disease. Common approaches include Matrigel-coated transwell systems, which mimic aspects of the tissue environment and allow researchers to assess invasive potential under controlled conditions. Using a cell invasion assay or combined cell migration & invasion assay, researchers can evaluate whether candidate therapies reduce invasive behaviour and limit processes associated with tumour progression and metastasis.

 

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Advanced oncology models

Traditional 2D cell cultures remain valuable for early-stage screening, but they often fail to capture the complexity of tumour biology seen in patients. As oncology programmes progress, more advanced models are needed to better reflect the cellular interactions, structural organisation and treatment responses found in vivo.

Advanced oncology models provide a more physiologically relevant environment for evaluating drug activity, mechanism of action and therapeutic potential. These systems can incorporate tumour architecture, microenvironmental factors and cell-cell interactions that influence treatment response. By bridging the gap between conventional cell culture and animal studies, translational models help researchers generate data that is more predictive of clinical outcomes. This can improve candidate selection, reduce development risk and provide greater confidence when advancing programmes through preclinical development.

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3D tumour spheroid models

Spheroids offer a practical way to model tumour behaviour in a more relevant 3D environment than standard monolayer cultures. By allowing cancer cells to grow as structured clusters, spheroid cell culture better reflects key features of the tumour microenvironment, including cell-cell interactions, gradients in oxygen and nutrients, and differences in drug penetration.

These factors can strongly influence treatment response, which is why spheroid models are widely used in preclinical oncology research. A spheroid formation assay or spheroid assay can help researchers assess growth, viability, morphology and compound activity in a setting that more closely resembles in vivo tumour biology.

Cancer spheroids are particularly useful when evaluating whether a therapy can reach and affect cells throughout a tumour-like structure, supporting more translationally relevant decision-making.

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PARP & DNA repair biology

DNA repair pathways help cells maintain genomic stability by detecting and repairing damaged DNA. PARP proteins play an important role in this process, particularly in the repair of single-strand DNA breaks. In cancers with defects in complementary repair pathways, such as BRCA-mutated tumours, blocking PARP activity can lead to synthetic lethality and selective tumour cell death. A PARP assay can be used to evaluate compound activity and pathway modulation, while PARP activity assay approaches provide insight into PARP enzymatic activity. These studies support the development and characterisation of targeted therapies, including PARP inhibitors.

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Immunogenic cell death

Some anti-cancer therapies do more than kill tumour cells; they also stimulate an immune response against the cancer. This process, known as immunogenic cell death, is characterised by the release of danger signals, or DAMPs, that alert and activate immune cells. Key markers include calreticulin exposure on the cell surface, ATP release and HMGB1 signalling. Immunogenic cell death assays help researchers measure these responses and assess the potential of new therapies to combine direct tumour killing with immune activation. These endpoints are increasingly important in the development of immuno-oncology strategies.

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Immuno-oncology research services

The success of modern cancer immunotherapies has highlighted the importance of understanding how tumours interact with the immune system. Effective drug development requires more than measuring tumour cell responses alone; it also depends on understanding immune activation, immune evasion and the mechanisms that influence treatment outcomes.

Cellomatics provides immuno-oncology CRO services that support the development of immunotherapies across discovery and preclinical research. Our capabilities help clients investigate tumour-immune interactions, evaluate immune-modulating compounds and generate translational data that supports candidate selection.

As an experienced immunotherapy CRO, we work with a range of advanced cellular models and assay platforms to study immune activation, checkpoint pathways and immunogenic cell death. These approaches are increasingly important for the development of checkpoint inhibitors and combination therapies designed to improve anti-tumour immune responses.

By combining oncology expertise with translational immune models, our team helps clients answer critical research questions and advance promising immuno-oncology programmes with greater confidence.

Oncology screening technologies

Oncology screening technologies help research teams look beyond simple measures of cell growth and understand how a compound is behaving in a biological system. For cancer drug discovery, this can mean assessing changes in viability, morphology, signalling, DNA damage, immune activation, migration or invasion across relevant tumour models.

Cellomatics uses a range of screening approaches to support oncology programmes, from targeted assay readouts to phenotypic screening and high-content imaging. The focus is not just on generating more data, but on producing results that help clients make clear decisions about which compounds to progress, refine or deprioritise.

By combining appropriate assay design with robust analysis, oncology screening can reveal mechanism of action, treatment response and potential liabilities earlier in development.

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Flow cytometry & cell phenotyping

Flow cytometry is widely used in oncology research to characterise tumour cells, profile immune populations and identify biomarkers associated with treatment response. By analysing multiple cellular markers simultaneously, researchers can gain a detailed understanding of complex biological systems and cellular heterogeneity. As a flow cytometry CRO, Cellomatics supports studies ranging from immune profiling and cell phenotyping to mechanism-of-action investigations. Our flow cytometry analysis CRO services help clients generate robust, multiparametric data that supports biomarker discovery, candidate selection and translational research across oncology programmes.

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Tumour profiling & biomarker discovery

Understanding why some patients respond to treatment while others do not is a major focus of modern oncology research. Tumour profiling helps researchers characterise disease biology, identify clinically relevant biomarkers and uncover mechanisms that influence treatment response. As a tumour profiling CRO, Cellomatics supports biomarker discovery and translational research using a range of cellular and molecular approaches. Our biomarker CRO services help clients identify markers associated with drug sensitivity, resistance and patient stratification, while biomarker discovery CRO studies provide valuable insights into mechanism of action and support more informed development decisions.

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Phenotypic screening & high content analysis

Phenotypic screening enables researchers to evaluate how compounds affect cellular behaviour without requiring a predefined target. By combining high-content imaging with quantitative analysis, these approaches can reveal changes in morphology, viability, signalling pathways and treatment response across large compound libraries. As a provider of phenotypic screening CRO services, Cellomatics helps clients identify and prioritise promising candidates based on functional biological outcomes. Our cell-based screening CRO services and screening assays CRO capabilities support both focused studies and large-scale campaigns, generating the data needed to make informed decisions and progress the strongest candidates through the drug discovery pipeline.

Phenotypic screening & high content analysis

Phenotypic screening enables researchers to evaluate how compounds affect cellular behaviour without requiring a predefined target. By combining high-content imaging with quantitative analysis, these approaches can reveal changes in morphology, viability, signalling pathways and treatment response across large compound libraries. As a provider of phenotypic screening CRO services, Cellomatics helps clients identify and prioritise promising candidates based on functional biological outcomes. Our cell-based screening CRO services and screening assays CRO capabilities support both focused studies and large-scale campaigns, generating the data needed to make informed decisions and progress the strongest candidates through the drug discovery pipeline.

Cancer models & therapeutic areas

No two cancer types behave in exactly the same way. Differences in tumour biology, genetic drivers, treatment response and interactions with the tumour microenvironment mean that selecting the right model is critical for generating meaningful preclinical data.

Cellomatics supports a broad range of oncology programmes using cancer models tailored to specific scientific questions and therapeutic objectives. Our experience spans both solid tumours and haematological malignancies, with expertise across breast cancer models, lung cancer models, colorectal cancer models and immuno-oncology models. Depending on the stage of development and study objectives, we work with established cancer cell lines, primary cancer cells and patient-derived models that provide greater clinical relevance.

Different therapeutic approaches require different assay strategies and oncology disease models. A targeted therapy programme may require detailed mechanism-of-action studies, while immunotherapy projects often depend on more complex immuno-oncology models that capture tumour-immune interactions. By combining biologically relevant systems with robust experimental design, our translational oncology models help researchers better understand drug activity, treatment response and resistance mechanisms.

Whether supporting early discovery, lead optimisation or translational research, we help clients select the most appropriate models to generate data that informs decision-making and supports successful programme progression.

Why choose Cellomatics for oncology research?

As a specialist provider of oncology CRO services, Cellomatics combines scientific expertise with the flexibility needed to support fast-moving drug discovery programmes.

  • Dedicated cancer drug discovery CRO with expertise across oncology assays, screening platforms and translational research.
  • Flexible study design and bespoke assay development tailored to specific scientific objectives.
  • Access to biologically relevant models, including primary human cells and advanced translational disease models.
  • Strong experience supporting both targeted therapies and immuno-oncology programmes.
  • High throughput screening capabilities for efficient compound evaluation and candidate prioritisation.
  • Direct access to experienced scientists throughout every project, ensuring clear communication and rapid decision-making.
  • Collaborative oncology research services designed to generate robust data that supports confident development decisions.

Our goal is simple: to provide scientifically rigorous, actionable data that helps clients move oncology programmes forward more efficiently.

FAQ's

What do Oncology Services include in research support?

Oncology CRO services cover a wide range of research activities that support cancer drug discovery and development. These can include oncology assays, assay development, phenotypic screening, high-content imaging, biomarker studies, tumour profiling and translational research. Many organisations also provide access to specialised models and technologies that help generate the data needed to make informed development decisions.

How do Oncology CRO Services support drug development?

A cancer drug discovery CRO helps researchers progress programmes from early target validation through to candidate selection. By providing specialist expertise, established workflows and preclinical oncology research capabilities, CRO partners can accelerate timelines, reduce internal resource requirements and generate robust data that supports critical development decisions.

What does a cancer drug discovery CRO focus on?

The choice of model depends on the scientific question being addressed. Common approaches include cancer cell lines, primary patient samples, spheroid models and other translational disease models designed to better reflect tumour biology. These oncology models help researchers evaluate drug activity, treatment response and mechanisms of resistance in more relevant experimental systems.

Which models are used in Oncology Services?

The choice of model depends on the scientific question being addressed. Common approaches include cancer cell lines, primary patient samples, spheroid models and other translational disease models designed to better reflect tumour biology. These oncology models help researchers evaluate drug activity, treatment response and mechanisms of resistance in more relevant experimental systems.

How do Oncology CRO Services improve study outcomes?

Oncology CRO services improve study outcomes by combining specialist expertise with appropriate model selection, assay design and data analysis. Through translational oncology research and advanced oncology screening services, researchers can generate more relevant biological insights, identify promising candidates earlier and make better-informed decisions throughout the drug discovery process.

Why choose a cancer drug discovery CRO for early-stage work?

Partnering with a cancer drug discovery CRO gives organisations access to specialised oncology research services without the need to build additional in-house capabilities. This can be particularly valuable during early-stage oncology drug discovery, where rapid access to expertise, screening platforms and translational models can help reduce risk and accelerate programme progression.

Request a consultation with Cellomatics Biosciences today

As part of our oncology CRO services, our experienced team of in vitro laboratory scientists will work with you to understand your project and provide a bespoke project plan with a professional, flexible service and a fast turnaround time.

To request a consultation where we can discuss your exact requirements, please contact Cellomatics Biosciences.