canSERV – Providing cutting edge cancer research services across Europe

Project Acronym canSERV
Funding Program HORIZON EUROPE
Budget € 14,866,440.50
Coordinator BBMRI-ERIC
Website https://www.canserv.eu/
Starting-ending date 1 September 2022 – 31 August 2025

The mission of the canSERVs project is to make cutting-edge and customised research services available to the cancer research community EU wide, enable innovative R&D projects and foster precision medicine for patients benefit across Europe. By connecting, coordinating, and aligning existing oncology and complimentary research infrastructures (RIs) and providing services in a synergistic way transnationally, canSERV will capitalise on the critical mass of experts and cutting-edge services offered by canSERVs RIs and their extended network.

CanSERV consortium

canSERV brings together world-class European life science RIs (BBMRI, EURO-BIOIMAGING, ELIXIR, EU-IBISBA, EuroPDX, EU-OPENSCREEN, INSTRUCT, EATRIS, INFRAFRONTIER, EMBRC, ECRIN, EATRIS, MIRRI, ARIE, CCE, EORTC and IARC) that collectively not only covers all aspects along the development pipeline for oncology, but is also capable of interconnecting these technologies providing users a guidance for navigating them through the entire translational value chain.

EATRIS role in the project

EATRIS in WP1 will provide access to disease models services (In vitro cancer model); the large portfolio of available cutting-edge cancer model services across service providers will be systematically and transparently categorised and catalogued by leading experts in cancer research.

EATRIS will lead the process to provide access to cutting-edge and high-quality services that will support the optimisation of existing screening programmes, the advancement of novel approaches for screening and early detection, identification of new biomarker sets, as well as will contribute to the development of novel therapeutics based on molecular predictors. In WP6, EATRIS will also provide expertise and guidance on regulatory requirements and methodological standards for personalised medicine research and will support the activities on innovation management to accelerate adoption in the Personalised Oncology domain.

EATRIS provided services catalogue

EMTBN service: European Molecular Tumour Board Network expert advice

Service provider: EATRIS

Regulatory Support Services

The EATRIS regulatory service will provide an assessment of the potential regulatory requirements required to prevent unnecessary project delays, reduce extra costs and most importantly prevent penalties resulting from non-adherence to legal requirements. EATRIS range of services includes:

  • Expert opinion and regulatory strategy planning
  • Pre-clinical and clinical development plan including TPP and IMPD
  • Informal scientific advice with selected national competent authorities, for highly complex projectsAccess to information about the regulatory requirements, guidelines and legislations from 27 EU countries (as well as Norway, Switzerland, Turkey and Israel) regarding drug and medical device development derived from the application of European legislation through the EATRIS Regulatory Database.

Service provider: EATRIS

Innovation Mangement Services

The EATRIS Innovation Helpdesk helps life science researchers access real-time legal support and partnering advice from the EATRIS community. Our Innovation management services include access to essential tools and resources for collaboration such as guidelines on intellectual property rights, open innovation and legal agreement templates. EATRIS Innovation Helpdesk services include:

  • Real-time advice
  • Template documents for frequently occurring technology transfer situations (MTA, CDA, etc)
  • Guidelines and assistance with cross-infrastructure, industry/academia collaboration and knowledge sharing
  • Access to specialist knowledge in relation to business development and legal and regulatory aspects
  • On a case-by-case basis, hands-on involvement by Innovation Office staff with real collaboration and negotiation cases

Service provider: EATRIS

Cancer Path Builder services

Service provider: EATRIS

Imaging evaluation of cancer preclinical murine models

Characterization and validation of murine models and/or cancer patients-derived xenograft through PET/TAC or bioluminescences/fluorescence (IVIS) imaging systems.

Service provider: Istituto Nazionale Tumori IRCCS “Fondazione G. Pascale” (INT – Pascale)

Imaging evaluation of murine model during cancer development and treatment

Advanced and quantitative in vivo MRI and MRS to characterize animal models of cancer in rodents during cancer development and following treatment. In particular: DWI with different diffusion models for functional characterisation, molecular imaging with iron oxide or 19F nanoparticles for macrofages recruitment studies and quantitative 1H, 31P and 19F MRS for cancer model metabolic characterisation.

Service provider: Istituto Superiore di Sanità (ISS)

Cell sorting of target population

Cell sorting of target population (e.g. rare population,..), identified by flow or mass cytometry in human tissues (MoFlow Astrios).

Service provider: Istituto Superiore di Sanità (ISS)

Immunocompetent murine models of cancer for antitumoral efficacy evaluation

Immunocompetent murine models of cancer for antitumoral efficacy evaluation, including effects on the tumour microenvironment. Expertise in (1) subcutaneous murine models of any type of cancer; (2) orthotopic immunocompetent models of fibrosarcoma or lung cancer, presenting a high infiltration of tumour-associated macrophages (i.e. MN/MCA or CMT167).

Service provider: Health Research Institute of Santiago de Compostela (IDIS)

Monochrome Multiplex Real-Time qPCR Assay for telomere measurement

Monochrome Multiplex Real-Time qPCR Assay for telomere measurement affected by incomplete DNA replication of a lagging strand or by the genotoxic effect of environmental and intracellular DNA-damaging agents, including anticancer drugs.

Service provider:  Institute of Experimental Medicine, Academy of Sciences of the Czech Republic

Comet assay (single-cell gel electrophoresis) for measuring DNA strand breaks and oxidative DNA damage

The comet assay (single-cell gel electrophoresis) is a simple method for measuring DNA strand breaks and oxidative DNA damage (Opattova, Horak et al. 2019). This method is applicable for human biomonitoring, testing novel chemicals for genotoxicity, environmental contamination with genotoxins and molecular epidemiology.

Service provider:  Institute of Experimental Medicine, Academy of Sciences of the Czech Republic

Assays for in vitro discovery research

Cell cycle, apoptosis, proliferation and phosflow assay for in vitro discovery research (i.e. drug discovery, pathway analysis)

Service provider: IRCCS SYNLAB SDN

MicroPET/CT acquisition dynamic on murine model

The service includes model generation (if possible in-house), animal handling, dynamic image acquisition and image post-processing. The radiotracer cost is included for radiotracers synthesized at our cyclotron or radiopharmacy facilities (18F-FDG, 18F-FLT, 18F-FMISO, 18F-choline,18F-DOPA, 68Ga-PSMA, 68Ga-DOTATOC). Unit of access includes animal housing and handling, radiotracer, and image processing after the experiment. Deliverables are: dynamic PET/CT images, full quantitative analysis report

Service provider: Health Research Institute of Santiago de Compostela (IDIS)

mAbs labelling: Labelling of novel mAbs with 89Zr for PET imaging

Service provider: Health Research Institute of Santiago de Compostela (IDIS)

Advanced Mass Spectrometry services for the Characterization of Molecular Tools

The service includes Protein/peptide identification, Antibody Characterization using Multi-Attribute Method (MAM), Post-Translational Modifications Analysis (Glycosylation; Oxidation/Deamination, Glycan Identity…), High-throughput Quantitative Proteomics – SWATH analysis (untargeted; relative quantification), Quantitative Proteomics/peptidomics – MRM-HR (targeted) (relative and/or absolute quantitation) and Intact Protein Measurement.

Service provider: Instituto de Biologia Experimental e Tecnológica (iBET)

Characterisation of Molecular Tools – Aggregation and refolding (SEC and RP chromatography)

Reverse phase (RP) and Size Exclusion Chromatography (SEC) to assess information on identity and purity attributes of protein-based biopharmaceuticals. SEC is applied for analysis of monomers, dimers, aggregates and degradation products according to their size. RP contributes to the characterization of the product in terms of hydrophobicity.

Service provider: Instituto de Biologia Experimental e Tecnológica (iBET)

Characterization of Immunophenotyping and Immunomonitoring

Cytokinomics analysis (48 Cytokines/chemockines) in human serum/plasma.

Service provider: Istituto Nazionale Tumori IRCCS “Fondazione G. Pascale” (INT – Pascale)

Biomarker’s validation (PET imaging)

The service provides the validation of clinical imaging biomarkers, especially assessing variability related with Physics and scanner-related effects. In particular, Monte Carlo simulation for producing realistic simulations of clinical images on different conditions (i.e. different scanners, reconstruction methods, noise conditions, etc…), is used to evaluate the estability of biomarkers over different conditions. The service provider developed the platform SimSET and has access to the CESGA supercomputing capabilities for the needed computational resources (https://www.cesga.es/en/home-2/)

Service provider: Health Research Institute of Santiago de Compostela (IDIS)

Targeted phospho-proteomics for studying the most relevant pathways in cancer

Targeted phospho-proteomics using 60 antibodies selectable among >400 covering the most relevant pathways in cancer, i.e. RTKs, PI3K/mTOR, MAPKs, autophagy, apoptosis, metabolism, cell adhesion and migration, cell cycle regulation and checkpoints, DNA damage, hypoxia as well as inflammation and immunity

Service provider: Istituto Superiore di Sanità (ISS)

Immuno proteomic profiling

Analysis of cytokine, chemokine and immune factors in human biological samples (serum, plasma, CSF, vitreous, saliva, tears, tumors samples) using Bio-Plex Assays -(Luminex thechnologies)

Service provider: Istituto Superiore di Sanità (ISS)

Sorting for Extracellular vescicles (Evs)

Analysis of fluorescent labelled EVs (cytoflex) – Sorting of fluorescent labelled EVs (MoFlow Astrios)

Service provider: Istituto Superiore di Sanità (ISS)

Mass Cytometry (Helios/Cytof XT)

Immune profiling with a fixed 30 antibody panel including barcoding (20-plex)

Service provider: University of Bergen

End-to-end analysis pipelines for radiogenomics studies (integration of biological and imaging biomarkers)

Radiogenomics is a discipline that identifies correlations between radiomic and dynamic parameters, as phenotypic data obtained from images can be correlated with tissue genome profiles and related molecular transcriptional activities. This service provides an end-to-end pipeline to perform such correlations by using statistical approaches and visual analysis of clusters (e.g., heat maps and dendrograms) with the objective to help the treatment selection by providing individual-level rather than population-level information.

Service provider: IIS La Fe

Multiparametric immunophenotype of blood/immune cells as well as solid tumour cells by flow cytometry

The service is intended for defining bone marrow and peripheral blood immune cells as well as solid tumor-infiltrating immune cells using state-of-the-art FCM protocols

Service provider: IRCCS SYNLAB SDN

Ultrasensite determination of biomarkers (i.e. circulating cytokines, Neurofilaments light chains, etc.) using the SIMOA technology for biomarker discovery and validation

The service is based on the SIMOA technology, a cutting-edge method for detecting circulating biomarkers. This technology also allows a fine detection of inflammatory cytokines in serum or plasma samples.

Service provider: IRCCS SYNLAB SDN

Isolation and characterisation of Circulating tumour cells (CTCs)

CellSearch system and DEPArray Nxt platform

Service provider: Istituto Nazionale Tumori IRCCS “Fondazione G. Pascale” (INT – Pascale)

cfDNA testing to evaluate the molecular profile and to monitor the response to therapy and the molecular evolution of the disease in cancer patients

Circulating free DNA testing using Next-Generation Sequencing platforms and Droplet Digital PCR technology for molecular profile assessment, disease monitoring and treatment response

Service provider: Istituto Nazionale Tumori IRCCS “Fondazione G. Pascale” (INT – Pascale)

Characterisation of immunophenotypes and immune-monitoring

Identification and quatification of the tumour immune infiltrate by flow cytometry, including Th1, Th2, Th17 and Treg cells, and their plasticity, cytotoxic T cells, γδ T cells, and double negative αβ T cells, M1 and M2 macrophages. Study of the expression of immunosuppressive molecules and/or their receptors by tumour cells, immune cells infiltrating the tumour, and their peripheral blood counterparts, including PD-1/PD-L1, IDO, CD39/CD73/A2A adenosine receptor (ADORA2A), CD200/CD200R, and TIM-3.

Service provider: Coimbra Hospital and University Centre (CHUC)

Immune monitoring-Immune-checkpoints panel: LAG3/ICOSL/CTLA-4/BTLA4/CD3/-/PD-1/CD4/PD-L1/

Service provider: Instituto de Investigación Sanitaria Valdecilla (IDIVAL)

Biomarkers discovery from liquid biopsies: exosomal microRNA (miRNA), ctDNA, and validation of miRNAs profiles

Analysis of miRNA, ctDNA and validation or miRNA profiles by RTqPCR

Service provider: IRCCS Istituto Giannina Gaslini (IGG)

Circulating Tuomor Cells Characterisation

Detection and characterisation of circulating tumor cells (phenotypic and copy number alteration and single nucleotide variations) , extracellular vesiscles (phenotypic and cargo), free circulating nucleic acids (gene mutation panel assay, shallow WGS, RNASeq, miRNASeq).

Service provider: IRCCS Istituto Romagnolo per lo Studio dei Tumori “Dino Amadori” – IRST Srl (IRST-IRCCS)

Development and analytical validation of multiplexed immunoassays for verification and validation of protein biomarkers in body fluids

The technologies implemented for de novo assay development are Luminex and Simoa (Quanterix). The affinity reagents used for assay development are tested for specificity. Further screening of antibodies to identify working antibody pairs for the biomarker of interest is part of the assay development. The cost includes analytical development and verification on ~400 samples. Cost however will depend on the number of biomarkers and assay type.

Service provider: KTH Royal Institute of Technology

Biomarkers Pre-analytical validation

Assessment and reporting of the robustness of your biomarker to common pre-analytical variables such as sample processing delays, storage and processing temperatures and freeze-thaw cycles

Service provider: The Integrated BioBank of Luxembourg (IBBL)

Biomarkers Analytical validation

Assessment and reporting of the analytical characteristics of your biomarker assay including, amongst others, precision, matrix effect, analytical range, specificity, sensitivity and stability.

Service provider: The Integrated BioBank of Luxembourg (IBBL)

Biomarkers clinical verification

Study on a limited sample size to verify the performance of your biomarker in clinical sample sets presenting the same clinical characteristics of the initial POC population.

Service provider: The Integrated BioBank of Luxembourg (IBBL)

Liver cancer platform for biomarker validation

Assessment and reporting of a specific biomarker in clinical samples of liver cancer. The technique used will depend on the nature of the biomarker (eg, in case of secreted proteins we will prioritize ELISA in plasma; in the case of gene expression biomarkers, we will study RNAseq data or qPCR data). The study includes a statistical analysis with clinical and pathological features to determine the diagnostic and prognostic potential of the selected biomarker.

Service provider: Germans Trias i Pujol Research Institute (IGTP)

Immunohistochemical validation of selected biomarkers

Automatised immunohistochemical staining for biomarkers assessment in human tissues. Samples usually correspond to paraffin blocks, including tissue microarrays, from formalin-fixed tissues. Immunohistochemistry on frozen tissue can be also considered upon agreement. This service does not include interpretation of the results.

Service provider: Germans Trias i Pujol Research Institute (IGTP)

Generation of vascularised tumoroid and organoids from endodermal derived tissues

Vascularised tumoroid and organoid generation with native blood vessels and large-scale expansion from endodermal derived tissues organoids.

Service provider: IIS Aragon

Generation of cell-based 3D diseases models

Biopsy derived cells to generate advanced 3D disease models (organoids or tumoroids) added with immune, stromal and endothelial cells.

Service provider: IIS Aragon

Microfluidic devices generation

Microfluidic devices for immune surveillance and drug testing.

Service provider: Istituto Superiore di Sanità (ISS)

Generation of 3D Hanging drop cancer microtissues, spheroids, organoids

Generation of 3D Hanging drop cancer microtissues, spheroids, and organoids, including cancer and stroma cells and/or macrophage co-cultured models.

Service provider: Istituto Nazionale Tumori IRCCS “Fondazione G. Pascale” (INT – Pascale)

Reprogramming of patient cells into iPSc

Reprogramming patient cells from blood samples or skin biopsies to iPSCs. Focus on patients harbouring mutations in cancer susceptibility genes.

Service provider: Instituto de Medicina Molecular (iMM)

Generation of organoids

Generation, expansion and validation of organoids from normal and neoplastic tissues.

Service provider: Istituto Superiore di Sanità (ISS)

Tumor-on-chip analysis

High throughput analysis of Tumor-on-Chip for dissecting the crosstalk between immune cells and cancer to obtain detailed morphodynamic and kinematic datasets. Automated high throughput analysis of cells (morphodynamic and kinematic parameters) and cell-cell interaction processing algorithms. Generation of ad hoc Matlab/R/ImageJ scripts for image optimisation and scaling.

Service provider: Istituto Superiore di Sanità (ISS)

Generation of cancer stem cell (CSC) model

Cancer stem cell (CSC) model generation to: i) understand the CSC dynamics, ii) track the efficacy of anti-CSC drugs and iii) evaluate the efficacy of CSC-targeted delivery systems. This model can be used to study the role of extracellular vesicles (EV) of CSC and non-CSC in tumour growth and dissemination.

Service provider: Vall d’Hebron Institute of Research (VHIR)

3D collagen biomimetic scaffolds generation

Study of tumour characteristics on -3D collagen biomimetic scaffolds on cancer cell lines and primary cells of solid tumours and in particular rare tumours as NEN, Sarcomas, H&N tumours, low-grade gliomas and bone metastases from solid tumours. -De-cellularised dermal scaffolds and 3-D scaffold free models multicellular (homotypic and heterotypic).

Service provider: IRCCS Istituto Romagnolo per lo Studio dei Tumori “Dino Amadori” – IRST Srl (IRST-IRCCS)

Organoid culture: Personalized Functional Profiling (PFP)

Analysis of the viability of ex-vivo tumor spheroids or organoids developed from the patient’s tumor sample in response to a selected drug panel. The functional drug response of the patient’s tumor spheroids/organoids is expected to provide treatment recommendations within 4-6 weeks (from the time of sample collection). This procedure is mainly applied for advanced-stage cancers.

Service provider: LIH-PFP

Digital Analysis Service plus expert support for EATRIS clinical cancer research support

Expert support and Digital Analysis service

Service provider: EATRIS

Design, production and validation of advanced nanotech-ATMP therapies

Design, production and validation of advanced therapies (ATMP) based on nanotechnologies for the delivery of proteins and RNA sequences to therapeutically manipulate the immune system

Service provider: Health Research Institute of Santiago de Compostela (IDIS)

Microfluidic device experiments and analysis

Fluidic or microfluidic devices for immune response and cell therapy testing.

Service provider: Istituto Superiore di Sanità (ISS)

Identification and quantification of the tumour immune infiltrate by flow cytometry

Identification and quantification of the tumour immune infiltrate by flow cytometry, including Th1, Th2, Th17 and Treg cells, and their plasticity, cytotoxic T cells, γδ T cells, and double negative αβ T cells, M1 and M2 macrophages. Study of the expression of immunosuppressive molecules and/or their receptors by tumour cells, immune cells infiltrating the tumour, and their peripheral blood counterparts, including PD-1/PD-L1, IDO, CD39/CD73/A2A adenosine receptor (ADORA2A), CD200/CD200R, and TIM-3.

Service provider: Coimbra Hospital and University Centre (CHUC)

Pre-clinical assessment of ATMPs in tumor cell models

Preclinical assessment of efficacy and specificity of advanced therapies in clinical relevant neuroblastoma models, such as orthotopic (well-established tumor in the adrenal gland), metastatic (circulating tumor cells and metastases), resected (surgical resection of the primary tumor mass for minimal residual disease), and PDX (Patient-Derived Xenografts) models.

Service provider: IRCCS Istituto Giannina Gaslini (IGG)

Synthesis and characterisation of nanoparticles

Service provider: IRCCS Istituto Romagnolo per lo Studio dei Tumori “Dino Amadori” – IRST Srl (IRST-IRCCS)

Study of ATMP efficacy

Service provider: IRCCS Istituto Romagnolo per lo Studio dei Tumori “Dino Amadori” – IRST Srl (IRST-IRCCS)

Allogenic NK CAR

Development and characterisation of Allogenic CAR NK cells from peripheral blood of healthy donors.

Service provider: Ospedale Pediatrico Bambino Gesù (OPBG)

Gene editing for complex CART cell engineering

Development and characterisation of CAR T cells optimised by the the gene editing of key elements regulating efficacy and persistence

Service provider: Ospedale Pediatrico Bambino Gesù (OPBG)

Generation of CAR-T Cells

Batches of frozen CAR-T cells can be generated from healthy donor T cells through retroviral transduction or mRNA transfection and frozen down in aliquots.

Service provider: UOH

Pre-clinical Assessment of CAR-T metabolism

Pre-clinical assessment of CAR-T Efficacy (Determination of the metabolic consumption of the CAR expressing cell).

Service provider: UOH

Live-cell imaging-based CAR-T killing assays

Evaluation of CAR-T, CAR-NK, CAR-NKT cell target killing efficacy (IncuCyte live-cell imaging of tumour cell spheroids or 2D cultures) using probes for measuring apoptosis.

Service provider: UOH

Bio-Plex: multiplex cytokine measurement

Evaluation of CAR-T, CAR-NK, CAR-NKT cytokine production, high-throughput multiplex immunoassay: Bio-Plex multiplex cytokine for measurement of cytokine levels in culture supernatant or serum/plasma samples.

Service provider: UOH

Characterisation of CAR-T, CAR-NK, CAR-NKT cell phenotype

Phenotyping of immune cells by mass cytometry (CyTOF), extracellular markers with around 35 marker panel including lineage markers, activation markers, exhaustion markers, memory markers. Intracellular staining can be performed, but will require validation.

Service provider: UOH

Animal Models for In vivo Validation of ATMPs

The animal facilities at iMM establish relevant cancer animal models for in vivo validation of ATMPs on a regular basis. Examples include acute myeloid leukemia (AML) induction, orthotropic colon cancer induction, cerebral metastases, subcutaneous cancer / tumor induction, mammary fat pad tumor induction, B16 melanoma model, different models for breast and pancreatic cancers.

Service provider: Instituto de Medicina Molecular (iMM)

In vivo validation of ATMPs design and planning

Histopathology for In vivo Validation of ATMPs: Pathology consultation – design and planning of animal studies; guidance in necropsy procedures; selection of fit-for-purpose histological and histochemical methods.

Service provider: Instituto de Medicina Molecular (iMM)

In vivo validation of ATMPs tumor volume

Histopathology for In vivo Validation of ATMPs: Histopathological analysis – efficacy evaluation by tumour volume including reporting.

Service provider: Instituto de Medicina Molecular (iMM)

In vivo validation of ATMPs bioluminiscence

Histopathology for In vivo Validation of ATMPs: Histopathological analysis – efficacy evaluation by bioluminescence imaging including reporting and capture of quality images.

Service provider: Instituto de Medicina Molecular (iMM)

Please note that if your CANSERV application is not successful, these services are also available on a fee-for-service basis from our access providers. Please also enquire about additional services that are available to support your cancer research programmes. Reach out for more information via our programme managers.

See all canSERV open calls here.

Download the flyer here or view it below.

Learn more about the Second Open Call on “Transnational Service Provision” here.