As a recent  article in the Journal of the American Medical Association noted this month, not all cancers are created equal. Some are less aggressive and easier to treat than others.Medical genetics

Now, as new tools to reveal these differences emerge, the JAMA article encourages researchers and clinicians to rethink screening for breast and prostate cancer.

Breast and prostate cancers now account for 26 percent of cancers in the United States.  However, in the last 20 years, it may be this increase in numbers reflects detection of low-risk growths that may never become dangerously cancerous.

One of the options the JAMA authors present is to focus on developing (and validating) markers that will identify significant from minimal risk cancers. These markers could target either the tissues that may be growing abnormally or the inherited genetic variants that may offer a person protection against these cancers. In Chapter 5 of our book, we discuss the differences between the genetic mutations that are a function of an abnormal cell line on the way to developing cancer, and genetic mutations that are inherited. It could be exciting to use genomics to direct personalized screening.

In this day and age of increasing health care costs, about $20 billion is spent to screen for breast and prostate cancer yearly. As new biomarkers are found and validated, the number of people who need screening or aggressive treatment might be reduced, and with it, the anxiety associated with hearing the word “cancer.”

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"As you read these pages, I hope you will be inspired to explore how you might use genetic information to improve your own health."
- Catherine Wicklund, MS, CGC
President, National Society of Genetic Counselors, 2007
from her foreword to The Genome Book

About the authors

April Lynch is an author whose work focuses on health and genetics. As an award-winning journalist, she directed coverage of science, health, and medicine for The San Jose Mercury News, Silicon Valley's leading newspaper. She has also written for a variety of other organizations, including leading university textbook publisher Pearson Education and genomics firm Navigenics. Her work on the book and this blog reflects her views, and not those of any employer or organization.


Vickie Venne, MS, CGC, is celebrating 30 years as a genetic counselor. She worked in prenatal, pediatric, and laboratory settings before joining the Hunstman Cancer Institute at the University of Utah. In addition to caring for patients, she has taught for the California Department of Education and the University of Utah's graduate program in genetic counseling. She has also served as president of the National Society of Genetic Counselors and the local affiliate of the Susan G. Komen Breast Cancer Foundation. Her work on the book and this blog reflects her views, and not those of any employer or organization.