National Institutes of Health U.S. Department of Health and Human Services
Cancer Genetics Branch Mission
The Cancer Genetics Branch (CGB) is part of the National Human Genome Research Institute, one of the 27 Institutes and Centers that constitute the National Institutes of Health. CGB was founded in 1993 and is one of several research branches within the Institute's Intramural Research Program that develops and utilizes state-of-the-art genomic-based technologies. The Branch applies these advances to cancer-related questions of public health concern. The primary focus of CGB investigators is to identify the genetic contribution to the processes of cancer susceptibility, tumor initiation and progression, treatment response, and long-term outcomes.
Specifically, the program:
Focuses on finding genetic relationships between regions of the human genome and cancer development, progression, response to treatment, and outcomes.
Conducts research on multiple types of cancer, including (but not limited to) cancers of the prostate, endometrium, lung, bladder, and breast; melanoma, and Fanconi anemia. These research efforts are conducted both independently and through collaborative agreements with universities, academic medical centers, and clinics.
Develops and maintains banks of normal and tumor tissue (consisting of both germline and tumor DNA) for a variety of types of cancer.
Identifies somatic genomic alterations that drive sporadic tumors using whole-exome and whole-genome sequencing approaches, expression profiling methodologies (such as RNA-seq), and copy number analysis.
Uses family-based studies and animal models to identify susceptibility loci, particularly for aggressive forms of common cancers. This involves using both linkage and genome-wide association studies of families and case-control studies. In addition we perform whole exome and genome sequencing of both germline DNA and tumors. Where applicable, we conduct pathway analysis of targeted genes.
Applies genomic technologies for molecular diagnosis of rare diseases with profound cancer susceptibility, such as Fanconi anemia.
Conducts individual and consortium-based collaborations with epidemiologists using genome-wide association studies to provide support for quality-of-life studies. We also work with both population scientists and clinicians to define gene profiles that offer predictability in terms of cancer susceptibility, metastasis, and outcomes.
Supports the development of genomic techniques specific for development of model organisms and the use of mouse and other small animal models for cancer-related genetic and functional studies.
Supports national collaborative efforts to expedite the search for cancer genes.
Trains clinicians, postdoctoral fellows, research associates, graduate students, and postbaccalaureate undergraduate trainees in the techniques and scientific processes related to the branch mission. The Branch is committed to training and providing opportunities to scientists from traditionally under represented groups.
Provides public education seminars and Continuing Medical Education lectures to support groups, clinicians, university departments, and other groups interested in the research being conducted by Branch Investigators.
Supports a multi-Institute microarray core that performs association and expression studies.
In summary, the scientists of the Cancer Genetics Branch work in a highly collaborative and multi-disciplinary setting to answer questions regarding the causes, growth patterns, and treatment responses associated with cancer. We are interested in defining and understanding the functional role of proteins involved in all phases of tumor development and growth for a variety of tumor types. Our long-term goal is to see our findings translated to advances in diagnosis and treatment. Finally, we utilize state of the art approaches in all phases of our work and we seek to develop and contribute advances in genomic technology to all fields of human health and biology.