Skip to Content

Alice J. Sigurdson, Ph.D.

Staff Scientist

Alice J. Sigurdson, Ph.D.

Alice J. Sigurdson, Ph.D.

Organization:National Cancer Institute
Division of Cancer Epidemiology & Genetics, Radiation Epidemiology Branch
Address:NCI Shady Grove
Room 7E524
Phone:240-276-7387
E-mail:sigurdsa@mail.nih.gov

Biography

Dr. Sigurdson received her Ph.D. from the University of Texas-Houston School of Public Health in 1997. Her post-doctoral training was in the Department of Epidemiology at The University of Texas M.D. Anderson Cancer Center. Following one year as an Instructor at M.D. Anderson she joined the NCI's Radiation Epidemiology Branch in 1999.

Research Interests

  • Molecular epidemiology of breast and thyroid cancer
  • Cosmic radiation exposures and cancer risk from medical imaging
  • Radiation exposure biomarkers
  • Radiosensitivity

One putative cause of human cancer is radiation exposure. Less well understood are inherent susceptibility factors that may disproportionately increase risk among individuals exposed to ionizing radiation. Chief leading candidates for radiation-related study are genes involved in the repair of DNA single and double strand breaks, since this is likely the most important genetic event caused by radiation to result in cell lethality, chromosomal aberrations and mutation. More agnostic approaches including genome-wide association studies (GWAS) will be used increasingly in the future. While few DNA repair genes have been identified by GWAS so far, denser gene coverage and including more rare variants may still yield important discoveries. In addition, I am interested in functional assays that might assess prospectively cancer risk of various sites.

Radiation Exposure and Radiosensitivity

Humans and animals are heterogeneous in their response to ionizing radiation exposure, both in terms of cancer susceptibility and acute tissue damage. For example, genes involved in DNA repair are known to be polymorphic and may confer unknown, but likely modified, function. Persons who carry specific single nucleotide polymorphisms (SNPs) or a collection of them, may be susceptible when exposed to endogenous or exogenous carcinogens, such as radiation. A single SNP can increase cancer risk, but considering the amount of overlap and redundancy in many cellular pathways, single sites of polymorphic variation may not account for many relationships with cancer outcome. But, multiple polymorphic sites in an individual could act in concert to increase or modify the radiation-related risk. In addition, a challenge-type biomarker of susceptibility that integrates multiple pathways may also be informative. We have pursued both these approaches in nested case-control studies of thyroid and breast cancers among our cohort of U.S. Radiologic Technologists.

Cosmic Radiation Exposures

In a collaborative effort with the National Institutes of Occupational Safety and Health, we are investigating breast cancer risk in a cohort of flight attendants who predominantly flew long-haul transcontinental routes. In addition, we will use fluorescence in situ hybridization (FISH) to evaluate stable chromosomal aberrations in senior airline pilots in relation to their radiation dose from flying commercial aircraft.

Radiation Exposure Biomarkers

Translocations in chromosomes detected by FISH are a measure of radiation exposure and also appear to be an intermediate marker for cancer risk. We have evaluated stable chromosome aberrations, specifically translocations, among a large cohort of radiologic technologists who were the most highly exposed (they worked before 1950 when exposures were the highest) and have affirmed our reconstructed dose estimates. In addition, we have used the translocation levels to detect cytogenetic damage related to radiation exposure from diagnostic x-ray examinations. Medical radiation exposure has collectively increased six-fold since the early 1980s and has now become a significant portion of the total radiation dose to the general public.

Information for Journalists

To request an interview with a DCEG investigator, contact the NCI Office of Media Relations:

E-mail:
ncipressofficers@mail.nih.gov

Phone: 301-496-6641