UNC Lineberger member and Associate Professor of Genetics, William Y. Kim, MD, and his colleagues report in the journal Nature Communications they have created mouse models of both papillary and clear cell renal cell carcinoma that faithfully mimic the genetic changes seen in tumors of patients with these cancers.
June 8, 2017
University of North Carolina Lineberger Comprehensive Cancer Center scientists have developed preclinical laboratory models of the two most common types of kidney cancer, an advancement that may aid in the evaluation of novel immunotherapy combinations and targets.
William Y. Kim, MD, a UNC Lineberger member and associate professor in the UNC School of Medicine, and his colleagues report in the journal Nature Communications they have created mouse models of both papillary and clear cell renal cell carcinoma that faithfully mimic the genetic changes seen in tumors of patients with these cancers. The researchers envision using the models to study new potential treatments, including possible immunotherapy approaches.
“Having faithful genetic models of kidney cancer will enable us to develop a better understanding of the biology behind these cancers,” said Kim. “We also can use these models to look for new targets and validate them in the preclinical setting more quickly as well as to test possible novel treatments that, if they work well, could be considered for patients with these genomic alterations.”
Kidney cancer is the eighth most commonly diagnosed cancer in the United States. The National Cancer Institute estimates 65,000 people will be diagnosed with kidney cancer in the U.S. this year, and it will account for 14,000 deaths. Approximately 70 percent of kidney cancer cases are clear cell renal cell carcinoma and 10 percent are papillary renal cell carcinoma.
“If there are certain therapies that seem to work in these models, we can identify these same genetic abnormalities in people with these cancer types, since they may be the most likely to benefit,” Kim said. “They will also be critical for testing new immunotherapy approaches, as these models have intact immune systems, which is something that has been limited in previous preclinical models of kidney cancer.”
Although several targeted treatments have been approved by the U.S. Food and Drug Administration for renal cell carcinoma, Kim said they target just two molecular pathways. Finding additional ways to attack kidney cancer using the models could be important for patients who have relapsed and are resistant to the existing treatments, he said.
In addition to Kim, other UNC authors include: Sean T. Bailey, Aleisha M. Smith, Jordan Kardos, Sara E. Wobker, Harper L. Wilson, Bhavani Krishnan, Ryoichi Saito, Jing Zhang, Samuel C. Eaton, Lindsay A. Williams, Ujjawal Manocha, Qing Zhang, Joel S. Parker, Jen Jen Yeh, Richard A. Moffitt, and Janet Y. Leung.