News Release

Additional inhibitor can help anti-VEGF therapy overcome resistance in deadly brain cancer

Penn study identifies target, shows proof-of-concept in mice

Peer-Reviewed Publication

University of Pennsylvania School of Medicine

PHILADELPHIA - Adding another inhibitor to therapies that cut off a tumor's access to blood vessels could be the key to helping those therapies overcome resistance in glioblastoma, a deadly form of brain cancer. Drugs that target the vascular endothelial growth factor (VEGF) - a signaling protein that stimulates the formation of blood vessels - are available but have yet to show an overall survival benefit in many malignant cancers. Now researchers from the Perelman School of Medicine at the University of Pennsylvania have shown the key may lie in adding an additional inhibitor that blocks the platelet-derived growth factor (PDGF), which regulates cell growth and division. The study not only identifies PDGF as a combination target for anti-VEGF therapies, but it also shows that pairing makes tumors more sensitive to anti-VEGF therapies in mice. Nature Communications published the findings today.

The American Cancer Society estimates there will be almost 24,000 diagnoses of malignant glioblastoma in the United States in 2018. It is the most common and most aggressive primary brain tumor, and patients have a median survival of about 14 months. One treatment approach involves targeting VEGF - most commonly with the drug bevacizumab -, with the idea being that cutting the tumor's access to blood vessels will cut off its supply of oxygen and nutrients it needs to survive.

A team led by senior author Yi Fan, MD, PhD, an assistant professor of Radiation Oncology at Penn, analyzed human glioblastoma specimens and found VEGF receptor expression was reduced in tumor-associated endothelial cells - the cells that line the interior surface of the blood vessels. In other words, the tumors are transforming the endothelial cells to make these cells resistant to anti-VEGF therapies. That's where the second inhibitor comes in. Researchers identified a PDGF pathway to knock out called PDGF/NF-κB/Snail. Blocking that pathway prevented the tumor endothelial cells from transforming, leaving the cancer vulnerable.

"This could be the key to solving the biggest problem in the field of anti-vascular cancer therapies," Fan said. "Tumors are highly resistant to anti-VEGF therapies alone, but our study shows the flaw is in the current treatment, not the concept itself."

Tianrun Liu, MD, PhD, a postdoctoral fellow in Fan's lab, is the study's lead author.

Since drugs already exist that can target both pathways, researchers put the combination to the test and showed that blocking both VEGF and PDGF improved overall survival in mice.

"These findings point the way toward a next generation of anti-VEGF therapies, opening the door to version 2.0," Fan said.

Fan noted that further research is needed to evaluate this combination in humans, as well as to look for other potential targets.

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The study was supported by the National Institutes of Health (R00HL103792, R01NS094533, R01CA190415), an American Association for Cancer Research Judah Folkman Award, a B*Cured Foundation Brain Cancer Investigator Award, and a McCabe Award.

Penn Medicine is one of the world's leading academic medical centers, dedicated to the related missions of medical education, biomedical research, and excellence in patient care. Penn Medicine consists of the Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania (founded in 1765 as the nation's first medical school) and the University of Pennsylvania Health System, which together form a $7.8 billion enterprise.

The Perelman School of Medicine has been ranked among the top medical schools in the United States for more than 20 years, according to U.S. News & World Report's survey of research-oriented medical schools. The School is consistently among the nation's top recipients of funding from the National Institutes of Health, with $405 million awarded in the 2017 fiscal year.

The University of Pennsylvania Health System's patient care facilities include: The Hospital of the University of Pennsylvania and Penn Presbyterian Medical Center -- which are recognized as one of the nation's top "Honor Roll" hospitals by U.S. News & World Report -- Chester County Hospital; Lancaster General Health; Penn Medicine Princeton Health; Penn Wissahickon Hospice; and Pennsylvania Hospital -- the nation's first hospital, founded in 1751. Additional affiliated inpatient care facilities and services throughout the Philadelphia region include Good Shepherd Penn Partners, a partnership between Good Shepherd Rehabilitation Network and Penn Medicine, and Princeton House Behavioral Health, a leading provider of highly skilled and compassionate behavioral healthcare.

Penn Medicine is committed to improving lives and health through a variety of community-based programs and activities. In fiscal year 2017, Penn Medicine provided more than $500 million to benefit our community.


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