Skip to main content

 

 

NCI Header
The Cancer Genome Atlas

Search GO

 

 


Expanded Program
  More information

Scientific Publications

View a growing list of scientific publications using TCGA Data.


National Cancer Institute National Human Genome Research Institute

Download as PDF

| Recovery Act Investment in
The Cancer Genome Atlas
Frequently Asked Questions

  1. What is The Cancer Genome Atlas (TCGA)?
  2. What are TCGA's goals?
  3. What types of cancer is TCGA studying?
  4. How do TCGA researchers find key genomic changes in cancer?
  5. Why is TCGA moving forward now?
  6. What are the accomplishments so far?
  7. How will TCGA use the American Recovery and Reinvestment Act funding?
  8. How will TCGA sustain itself beyond the Recovery Act?
  9. How can people with cancer support TCGA?
  10. Where can I find additional information about TCGA?

 

  1. What is The Cancer Genome Atlas (TCGA)?
    The Cancer Genome Atlas (TCGA) is a large-scale, collaborative effort by the National Institutes of Health (NIH) to create a comprehensive collection of maps that chart the genomic changes that occur in each type of cancer. This atlas will serve as a valuable resource for researchers around the world, accelerating their efforts to develop new and better ways of fighting cancer.

    Administered by the National Cancer Institute (NCI) and the National Human Genome Research Institute (NHGRI), the project involves more than 150 researchers working together at dozens of institutions across the nation.

    Back to Top

  2. What are TCGA's goals?
    TCGA's goal is to comprehensively map the important genomic changes involved in the major types and subtypes of cancer. By making all data and analytical tools swiftly available to the research community through public databases, TCGA will accelerate the pace of research aimed at improving cancer diagnosis, treatment and prevention.

    Back to Top

  3. What types of cancer is TCGA studying?
    Based on the success of a three-year pilot effort that involved brain (glioblastoma multiforme), lung (squamous carcinoma) and ovarian (serous cystadenocarcinoma), NIH announced in September 2009 that TCGA will study more than 20 additional types of cancer over the next five years. NCI and NHGRI have not yet determined the specific types of cancer that will be part of the expanded effort.

    Factors that will be considered include: a cancer's frequency and severity, existence of effective treatments and availability of high-quality tissue samples. TCGA will also take into account cancer genome mapping efforts in other nations. To learn more about cancers being mapped by TCGA, go to: http://cancergenome.nih.gov/wwd/cancers_studied_by_tcga.asp.

    Back to Top

  4. How do TCGA researchers find key genomic changes in cancer?
    TCGA researchers identify a cancer's key changes by comparing the genomic material in tumor samples from hundreds of patients with genomic material in healthy tissue samples from the same patients.

    This comparison is carried out using high-throughput technologies and methods that look for: small changes in DNA sequence, known as genetic mutations; larger-scale changes in chromosomes, known as copy number variations and chromosomal translocations; changes in gene expression, which is reflected in levels of RNA, a protein-coding molecule produced by genes; and epigenomic changes, which involve patterns of how certain molecules, such as methyl groups, interact with DNA. Researchers also integrate clinical information related to the patients' treatment and outcome into their analyses.

    For more details on how the various components of TCGA contribute to comprehensive characterization and analysis efforts, go to: http://cancergenome.nih.gov/wwd/program/.

    Back to Top

  5. Why is TCGA moving forward now?
    Several important advances indicate that now is the ideal time for NIH to move forward with TCGA. First, the technologies used to determine the sequence of genomic DNA have undergone a revolutionary change in the last several years. It is now feasible, technically and economically, to consider characterizing entire genomes comprehensively across many hundreds or thousands of cancer samples.

    A second advance centers on the increasing evidence that comprehensive knowledge of cancer's genomic changes can lead to more effective diagnosis, treatment and prevention. "Proofs of concept" include the success of new molecularly targeted drugs, such as Gleevec for chronic myeloid leukemia, and the development of genetic tests to identify subsets of cancer patients most likely to respond to chemotherapy drugs, such as Iressa and Tarceva for lung cancer.

    A third advance is the availability of the human genome sequence and other genome reference sets. These public databases provide an excellent starting point to compare genomic data derived from various cancers.

    Because cancer is a disease caused by genomic changes, TCGA represents the grandest opportunity to apply biomedical research's newfound knowledge and technologies to an area of terrible disease and suffering. Consequently, NCI and NHGRI are obligated to tackle more cancers now, a course of action made possible through the investment provided by the American Recovery and Reinvestment Act.

    Back to Top

  6. What are the accomplishments so far?
    Over the course of a three-year pilot project started in 2006, NCI and NHGRI successfully established the policies, infrastructure, production pipelines, collaborative networks and public databases needed for TCGA's large-scale, systematic approach to identifying genomic changes in cancer.

    In a paper published in the journal Nature [455, 1061-1068, 3 October 2008], the pilot's research network reported the first results of its integrated, multi-dimensional analysis of the brain cancer glioblastoma. The landmark study identified three new mutations that occur with significant frequency in glioblastoma and delineated core pathways disrupted in this type of brain cancer. One of the most exciting results was an unexpected observation that points to a potential mechanism of resistance to a common chemotherapy drug used for brain cancer. Read the paper at: http://cancergenome.nih.gov/objects/pdfs/nature07385.pdf.

    Also as part of the pilot, researchers have recently characterized the ovarian cancer genome. These data, which are now being analyzed for publication, are avaliable through the TCGA Data Portal, http://cancergenome.nih.gov/dataportal/data/about.

    Back to Top

  7. How will TCGA use the American Recovery and Reinvestment Act funding?
    TCGA has received $175 million in Recovery Act funding that will enable it to study more than 20 types of cancer.

    Specifically, Recovery Act funds will be used to help support the Genome Characterization Centers, to acquire and prepare tissues from cancer patients, to further develop databases and to enhance analytical tools and activities. In addition, DNA sequencing methods and technologies will be expanded to include targeted sequencing of larger numbers of genes and the sequencing of entire cancer genomes.

    TCGA's effort will require a significant increase in the number of people in the academic, non-profit and private sectors working collaboratively to generate, analyze and utilize the data. This will lead to the retention and creation of a substantial number of diversified jobs.

    Recovery Act funding will also support technological and computational innovations in the area of cancer research, fueling a new generation of scientific discovery. Such an investment will continue to impact the U.S. economy — and research and development — for years to come, and will likely have a positive impact on diseases well beyond cancer.

    Back to Top

  8. How will TCGA sustain itself beyond the Recovery Act?
    NCI and NHGRI regard TCGA as a high-priority program and will continue to support it through regular budget allocations beyond the Recovery Act's two-year funding period. In addition to $18 million per year for data generation and analysis, the NCI will need to provide significant funding for tissues and sample processing to sustain the project. For its part, NHGRI will need to ensure that its NHGRI-funded large-scale sequencing centers allocate enough capacity to meet TCGA's needs.

    Back to Top

  9. How can people with cancer support TCGA?
    Samples of healthy and cancerous tissue are essential for TCGA and many other types of cancer research going on across the country. So, donating your tissue can be a very important gift to the research process. If you are considering donating your tissue, a good first step would be to ask your doctors whether they are taking part in cancer research or partnering with cancer research groups. Keep in mind that it often is not possible to select the specific research projects in which your sample will be used.

    Back to Top

  10. Where can I find additional information about TCGA?
    For more information about TCGA, please visit http://cancergenome.nih.gov/.

    Back to Top

 

National Cancer InstituteNational Human Genome Research InstituteNational Institutes of HealthDepartment of Health and Human ServicesFirstGov.gov