By Yi Yin, PhD, Damon Runyon Fellow, University of Washington

The Damon Runyon Cancer Research Foundation recently asked some of our current award recipients how cancer will be prevented, diagnosed, and/or treated differently in the future. What can a future cancer patient, say 10-20 years from now, expect to experience? Their responses were fascinating, and over the next few months we will share their visions for the future on this blog.

I think cancer will be prevented, diagnosed and/or treated very differently within the next 10-20 years.

Anjana Rao, PhD (Damon Runyon Fellow ’79), and James Scott-Browne, PhD (Damon Runyon Fellow ’11-’13), at the La Jolla Institute for Allergy and Immunology, La Jolla, and colleagues, are focusing on a key issue of how tumor-fighting T cells can lose their effectiveness or become “exhausted.”  The researchers identified two proteins, NFAT and Nr4a, that can bind to the DNA of T cells and shut down their tumor-fighting activity.  Next steps will be to determine if these processes can be interfered with or reversed in ord

The Damon Runyon Cancer Research Foundation recently asked some of our current award recipients how cancer will be prevented, diagnosed, and/or treated differently in the future. What can a future cancer patient, say 10-20 years from now, expect to experience? Their responses were fascinating, and over the next few months we will share their visions for the future on this blog.

By Amanda Balboni, PhD, Damon Runyon Sohn Fellow at the Dana-Farber Cancer Institute

In the next 10-20 years, I anticipate that tumor genetic testing will become standard practice as sequencing technology becomes faster and more cost effective. This will revolutionize the way cancer is treated clinically and make personalized cancer medicine a reality. 

Don X. Nguyen, PhD (Damon Runyon Fellow ’05-’08), of Yale Cancer Center, New Haven, and colleagues, reported new findings that explain the propensity of latent lung adenocarcinoma (LUAD) to relapse. They showed that differential expression of extracellular matrix (ECM) molecules and their interacting proteins contributes to risk of relapse in distinct LUAD subtypes. One protein called hyaluronan receptor HMMR, when overexpressed, was associated with inflammation and poor prognosis.

By Megan Insco, MD, PhD, Damon Runyon Fellow at Boston Children's Hospital

When I was in 7th grade, my mother was diagnosed with breast cancer.  I was devastated and directionless.  When she passed away two years later, my broad set of interests resolved around a singular focus.  I would channel my passion for discovery and my need to see my work manifest productively in the world, into a career discovering and delivering life-enhancing therapies for cancer patients. 

Christine Iok In Chio, PhD (Damon Runyon Shirley Stein Fellow ’13-’17), in the laboratory of her sponsor David Tuveson, MD, PhD, and colleagues at Cold Spring Harbor Laboratory, Cold Spring Harbor, created a new 3D model of pancreatic cancer, which allowed them to identify two distinct stroma cell populations called cancer-associated fibroblasts  (CAF’s), that work together with cancer cells to protect and help the tumor grow.

Today we realize that cancer is not a single disease, but something unique to each individual. Even within a single tumor there is complexity and diversity unrecognized just a decade ago.

Employing this knowledge, along with emerging technological advances, will lead to fundamental changes in the patient population. To this end, more sensitive and specific diagnostics will greatly reduce the number of late-stage cancer diagnoses. This early detection, along with an increasing breadth of cancer therapeutics, will revolutionize the way we assess clinical outcomes.

An important reason why the United States is the global leader in biomedical research is that many of the best scientific minds from around the world come here to train and work.  If you walked into any leading US research laboratory today, you would meet scientists from many countries working together as a team to solve the greatest scientific challenge of all time – understanding human biology and ending suffering from disease.  These labs are meritocracies and melting pots.  Most importantly, they generate knowledge that drives our entire health care enterprise and saves lives.

By Victoria E.H. Wang, MD, PhD, Damon Runyon Fellow, University of California, San Francisco

The Damon Runyon Cancer Research Foundation recently asked some of our current award recipients how cancer will be prevented, diagnosed, and/or treated differently in the future. What can a future cancer patient, say 10-20 years from now, expect to experience? Their responses were fascinating, and over the next few months we will share their visions for the future on this blog.

Lorraine W. Egan, President and CEO, Damon Runyon Cancer Research Foundation

Gregg Gordon was 44 and the picture of health until he suddenly became excessively tired and noticed two small bumps on his shin. A visit to his doctor led to a startling cancer diagnosis, and less than 24 hours later he was receiving chemotherapy to treat acute myeloid leukemia.

When standard treatments failed, Gregg’s best hope was a bone marrow transplant, but he could not find a donor match. Fortunately, he was referred to Colleen Delaney, MD, in Seattle, who had developed a process for expanding stem cells from umbilical cord blood for use in patients without donors. As The Washington Post reported in September, the procedure was a success and Gregg has been cancer-free for five years.