Researchers at the Medical College of Wisconsin (MCW), in collaboration with other colleagues of the Genetic Epidemiology of Lung Cancer Consortium (GELCC), have identified a gene that is associated with lung cancer.
The findings are published in American Journal of Human Genetics. Through whole exome sequencing, researchers identified a link between a mutation in PARK2, a gene associated with early-onset Parkinson's disease, and familial lung cancer.
The researchers sequenced the exomes (protein coding region of the genome) of individuals from a family with multiple cases of lung cancer. They then studied the PARK2 gene in additional families affected by lung cancer.
"While this specific mutation is very rare in the general population, there was a significant association between the PARK2 mutation we studied and the families with multiple cases of lung cancer," said Donghai Xiong, PhD, assistant professor of pharmacology and toxicology at MCW and the lead author on the paper.
"These results implicate this specific mutation as a genetic susceptibility factor for lung cancer, and provide an additional rationale for further investigations of this gene and this mutation for evaluation of the possibility of developing targeted therapies against lung cancer in individuals with PARK2 variants," added Ming You, MD, PhD, the Joseph F. Heil Jr. Professor of Oncogenesis at MCW and Director of the MCW Cancer Center.
The GELCC is headed by Dr. Marshall Anderson, PhD, professor of medicine at MCW. Other GELCC collaborating institutions include the National Human Genome Research Institute, the University of Cincinnati College of Medicine, the University of Toledo College of Medicine, the Louisiana State University Health Sciences Center, the Karmanos Cancer Institute in Detroit, Mich., the Mayo Clinic, the Geisel School of Medicine at Dartmouth College, the University of Pennsylvania, and the Baylor College of Medicine in Houston, Tex.
American Journal of Human Genetics