Scientists at the University of North Carolina Lineberger Comprehensive Cancer Center in Chapel Hill, NC, 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, according to an article published in the journal Nature Communications.
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William Y. Kim, MD, a UNC Lineberger member and associate professor in the UNC School of Medicine, and his colleagues explained that they 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,” noted Dr. 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 that 65,000 people will be diagnosed with kidney cancer in the US this year, and it will account for 14,000 deaths. Approximately 70% of kidney cancer cases are clear cell renal cell carcinoma and 10% 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,” Dr. 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 US Food and Drug Administration for renal cell carcinoma, Kim noted that 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.
“There is still a lot of room for drug development and target validation in other cancer signaling pathways that have gone awry,” Dr. Kim said.
In addition to creating research tools that could be key to future research, the study also exposed the importance of a gene called MYC in the development of kidney cancer. By activating MYC alone, researchers were able to create a papillary kidney cancer model. To create a model of clear cell kidney cancer, study authors activated MYC and deleted two other genes. While fewer than 6% of patients with clear cell renal cell carcinoma have been found to have all three of these genomic alterations, the researchers believe that the models may help test potential new treatments for patients with the clear cell subtype that have similar genomic alterations.
In addition to Kim, other authors include: Sean T. Bailey, Aleisha M. Smith, Jordan Kardos, Sara E. Wobker, Harper L. Wilson, Bhavani Krishnan, Ryoichi Saito, Hyo Jin Lee, Jing Zhang, Samuel C. Eaton, Lindsay A. Williams, Ujjawal Manocha, Dorien J. peters, Xinchao Pan, Thomas J. Carroll, Dean W. Felsher, Vonn Walter, Qing Zhang, Joel S. Parker, Jen Jen Yeh, Richard A. Moffitt, and Janet Y. Leung.
The study was supported by the National Institutes of Health, AACR Kure It, Damon Runyon Cancer Research Foundation and a UNC Lineberger Developmental Research Award.