Human Cancer Model Initiative (HCMI)

Human Cancer Model Initiative (HCMI)

Human Cancer Model Initiative (HCMI)

The Human Cancer Model Initiative is an international collaboration to develop the next-generation of cancer cell models as a resource for the scientific community.

About the Partnership

The Human Cancer Model Initiative (HCMI) is an international effort to develop the next-generation of cancer cell models that better represent the hallmarks and diversity of human cancer. Our laboratory is taking a leadership role in this initiative in collaboration with the Cancer Research UK, the U.S. National Cancer Institute, and the foundation Hubrecht Organoid Technology. At the Sanger Institute, we will derive and genetically characterise hundreds of new organoid models and make them available to researchers as a transformative resource for the community.

Approximately 1,000 human cancer cell lines are available to scientists worldwide and these are a useful resource for cancer research and drug development. Over the past decade the Sanger Insitute has played a central role in the genetic analysis of a large number of human cancer cell lines through the COSMIC cell line project. These cell lines have been used extensively for modelling drug response as part of the Genomics of Drug Sensitivity in Cancer project to identify molecular alterations in cancer which impact on drug sensitivity. This information can be used to understand the variation observed in patient responses to treatment and to help guide the development of new more effective and less toxic cancer therapies for the future.

As we enter the era of precision medicine, treating molecularly defined patients, poor representation of some cancer types, insufficient numbers to capture the genetic diversity of cancer, lack of clinical outcome data and lack of comparison to normal reference sample limit the use of the current set of cell lines. Novel cell culturing methods such as organoid derivation have revolutionised our ability to derive cell line models from both healthy and diseased tissue, and have the potential to overcome these limitations.

The Contribution of WTSI and CRUK to the HCMI

Organoids are a long-term culture system which allow cells to be grown in specialised 3D culture conditions that maintain the stem cell population as well as much of the cell/tissue architecture found in vivo. Cancer organoid models have been shown to recapitulate features of the original tissue/tumour and can model clinically relevant drug responses. Through generating large numbers of molecularly characterised organoid models, and performing drug sensitivity screens, we aim to identify new cancer treatments.

organoid.jpgSanger Institute, Genome Research Limited
Oesophageal cancer organoid

As part of the HCMI, the Sanger Institute has joined forces with Cancer Research UK (CRUK) to derive approximately 250 organoid cell models from colon, oesophageal and pancreatic cancers. These models are being generated from patient samples taken at the time of surgical resection and will include a subset of patient-matched normal organoid models. CRUK have provided access to their unique clinical network allowing access to clinical samples as well as the collection of clinical data.

These models will be derived at the Sanger Institute and will be highly annotated including a complete sample history and key pieces of patient clinical information. The original tumour as well as the matched organoid culture will also be genomically characterised and drug screens performed. These new cell models and associated datasets be shared with the research community to further research in cancer and other diseases.

Project Questions

As part of a pilot phase, over the next two years the Sanger Institute and CRUK will critically evaluate the utility of organoids as cancer models by addressing the following questions:

  • How does organoid derivation compare with other cell derivation methods?
  • Are organoid cultures genetically and phenotypically stable in cultures over time?
  • How well do organoid cultures capture genetic changes observed in patients?
  • Are organoids a useful tool for modelling drug response observed clinically?
  • Can we develop the infrastructure and improve derivation processes to increase success rates and reduce costs?

Our findings will help establish the utility of organoids as a model system for studying cancer and could pave the way for derivation of an even larger number of models to encompass the genetic diversity of cancer.

Our work, as part of the HCMI, will provide the research community with the next-generation of cancer cell models and by working together will accelerate this process in a cost-effective, streamlined and unified way, allowing for rapid learning, protocol sharing and standardised practices while avoiding duplication of efforts.

Sanger Team Partners

Related Tools and Data

Partners and Funders

Publications

  • Prospective derivation of a living organoid biobank of colorectal cancer patients.

    van de Wetering M, Francies HE, Francis JM, Bounova G, Iorio F et al.

    Cell 2015;161;4;933-45

  • What role could organoids play in the personalization of cancer treatment?

    Francies HE and Garnett MJ

    Pharmacogenomics 2015;16;14;1523-6

  • Systematic identification of genomic markers of drug sensitivity in cancer cells.

    Garnett MJ, Edelman EJ, Heidorn SJ, Greenman CD, Dastur A et al.

    Nature 2012;483;7391;570-5

  • Long-term culture of genome-stable bipotent stem cells from adult human liver.

    Huch M, Gehart H, van Boxtel R, Hamer K, Blokzijl F et al.

    Cell 2015;160;1-2;299-312

  • Organoid models of human and mouse ductal pancreatic cancer.

    Boj SF, Hwang CI, Baker LA, Chio II, Engle DD et al.

    Cell 2015;160;1-2;324-38

  • Long-term expansion of epithelial organoids from human colon, adenoma, adenocarcinoma, and Barrett's epithelium.

    Sato T, Stange DE, Ferrante M, Vries RG, Van Es JH et al.

    Gastroenterology 2011;141;5;1762-72

  • Organoid cultures derived from patients with advanced prostate cancer.

    Gao D, Vela I, Sboner A, Iaquinta PJ, Karthaus WR et al.

    Cell 2014;159;1;176-87

  • ROCK inhibitor and feeder cells induce the conditional reprogramming of epithelial cells.

    Liu X, Ory V, Chapman S, Yuan H, Albanese C et al.

    The American journal of pathology 2012;180;2;599-607