CHAMPAIGN, Ill. — Scientists have identified a potential driver of aggressive lung cancer tumors in patients who live in areas with high levels of violent crime. Their study found that stress responses differ between those living in neighborhoods with higher and lower levels of violent crime, and between cancerous and healthy tissues in the same individuals.
The findings are detailed in the journal Cancer Research Communications.
Photo by Jonathan King/Cancer Center at Illinois
The study was designed to address the higher incidence of lung cancer in Black men than in white men, according to University of Illinois Urbana-Champaign food science and human nutrition professor and Carle Illinois College of Medicine Associate Professor Zeynep Madak-Erdogan. She led the research with University of Illinois Chicago School of Public Health health policy and administration professor Sage Kim, the principal investigator of the project. This disparity persists even though, on average, Black men smoke less and start smoking later in life than white men, Kim said.
In another study, Kim and her team found that Black men living in Chicago zip codes with higher violent crime rates had substantially higher levels of hair cortisol — one indicator of chronic stress — than those in areas with less violent crime.
Other studies have linked chronic exposure to stress to poorer outcomes in cancer patients, Madak-Erdogan said. But scientists’ understanding of how stress “gets under the skin” to influence lung cancer prognosis is limited.
The newer analysis focused on glucocorticoids, a group of steroid hormones like cortisol.
These hormones bind to receptors that regulate the activity of other genes. Glucocorticoids and their receptors are involved in a variety of key functions, Madak-Erdogan said. They help regulate fetal and newborn lung tissue development, and play a role in metabolism, homeostasis, inflammation, and immune function in this tissue.
The researchers first assessed patterns of gene expression in lung cancer tumors and in cancer-free lung tissue from patients who lived in various Chicago zip codes — some with higher or lower levels of violent crime. The team also determined where the glucocorticoid receptors were binding on DNA in those tissues.
Both analyses revealed that GR binding and gene-expression patterns were different in healthy versus tumor tissues, and that the patterns also differed by a patient’s zip code. Overall, GR binding was highest in people who lived in high-violence areas. But within the tumor tissues, those living in high-crime zip codes had lower GR binding. They also had lower levels of GR-regulated genes in the tumor tissues.
The analyses also revealed that, within tumors, the GRs were activating genes for enzymes that degrade cortisol. This accounted for the lower cortisol levels — thus lower GR binding — in the tumors than in normal lung tissue. The lower cortisol levels were likely influencing the overall behavior of the receptors in the lung cancer tumors, Madak-Erdogan said.
“In terms of the genes the receptors regulated in the tumors of individuals living in high-violence areas, they were genes related to inflammation, higher proliferation, higher growth-factor signaling, all of which will lead to the worst outcomes for lung cancer,” she said. “While we didn’t prove a direct relationship in this study, our findings suggest that glucocorticoids and glucocorticoid receptors are a main driver of adverse tumor outcomes in patients living with chronically high levels of environmental stress.”
The study accounted for other factors, such as environmental risk and poverty, that might lead to worse health outcomes in people living in high-crime areas, Kim said. It found no consistent correlation between poverty or environmental risk and lung cancer in the neighborhoods of interest.
Prior to the new study, scientists suspected that stress hormones played a role in cancer or other health disparities, Madak-Erdogan said. “But we didn’t know the exact role they play, or how they work to drive lung cancer progression. I think this study really crystallizes the idea that it’s not just that individuals in these areas are more stressed. It’s also that their stress responses are dysregulated. There is a direct effect of these hormones on the normal cellular physiology.”
Madak-Erdogan is an associate professor at CI MED and a professor in the Carl R. Woese Institute for Genomic Biology and the National Center for Supercomputing Applications at the U. of I. She also is the associate director for education in the Cancer Center at Illinois. U. of I. graduate student Hannah Heath is the first author of the paper.
The National Institute of Minority Health and Health Disparities at the National Institutes of Health supported this research.
Editor’s notes:
To reach Zeynep Madak-Erdogan, email zmadake@illinois.edu.
To reach Sage Kim, email skim49@uic.edu.
The original version of this article by the Illinois News Bureau can be found here.