TY - JOUR
T1 - The effect of exposure to neighborhood violence on Glucocorticoid Receptor signaling in lung tumors
AU - Heath, Hannah
AU - Yoo, Jin Young
AU - Akter, Sabrina
AU - Jain, Atharva
AU - Sharma, Vani
AU - McGee, Hannah
AU - Soliman, Aiman
AU - Mahmoud, Abeer M.
AU - Matthews, Alicia K.
AU - Winn, Robert A.
AU - Madak-Erdogan, Zeynep
AU - Kim, Sage J.
N1 - This work was primarily supported by 5R01MD014839 (MPIs SK, RW) from the National Institute of Minority Health and Health Disparities (NIMHD); the UIUC Graduate College and Endocrine Society\u2019s Research Experience for Graduate and Medical Students Fellowships supported H. Heath; T32EB019944 from the National Institute of Biomedical Imaging and Bioengineering (NIBIB) supported J.Y. Yoo; and the Illinois Computes program to Z. Madak-Erdogan and A. Soliman.
All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Z. Madak-Erdogan reports grants from NIH during the conduct of the study; grants from Karyopharm Therapeutics outside the submitted work. No other disclosures were reported.
PY - 2024/7
Y1 - 2024/7
N2 - Despite lower rates and intensity of smoking, Black men experience a higher incidence of lung cancer compared to white men. The racial disparity in lung cancer is particularly pronounced in Chicago, a highly segregated urban city. Neighborhood conditions, particularly social stress, may play a role in lung tumorigenesis. Preliminary studies indicate that Black men residing in neighborhoods with higher rates of violent crime have significantly higher levels of hair cortisol, an indicator of stress response. To examine the relationship between social stress exposure and gene expression in lung tumors, we investigated glucocorticoid receptor (GR) binding in 15 lung tumor samples in relation to GR target gene expression levels and zip code level residential violent crime rates. Spatial transcriptomics and a version of ChIP sequencing known as CUT&RUN were used. Heatmap of genes, pathway analysis, and motif analysis were conducted at the statistical significance of P < 0.05. GR recruitment to chromatin was correlated with zip code level residential violent crime rate and overall GR binding increased with higher violent crime rates. Our findings suggest that exposure to residential violent crime may influence tumor biology via reprogramming GR recruitment. Prioritizing lung cancer screening in neighborhoods with increased social stress, such as high levels of violent crime, may reduce racial disparities in lung cancer.
AB - Despite lower rates and intensity of smoking, Black men experience a higher incidence of lung cancer compared to white men. The racial disparity in lung cancer is particularly pronounced in Chicago, a highly segregated urban city. Neighborhood conditions, particularly social stress, may play a role in lung tumorigenesis. Preliminary studies indicate that Black men residing in neighborhoods with higher rates of violent crime have significantly higher levels of hair cortisol, an indicator of stress response. To examine the relationship between social stress exposure and gene expression in lung tumors, we investigated glucocorticoid receptor (GR) binding in 15 lung tumor samples in relation to GR target gene expression levels and zip code level residential violent crime rates. Spatial transcriptomics and a version of ChIP sequencing known as CUT&RUN were used. Heatmap of genes, pathway analysis, and motif analysis were conducted at the statistical significance of P < 0.05. GR recruitment to chromatin was correlated with zip code level residential violent crime rate and overall GR binding increased with higher violent crime rates. Our findings suggest that exposure to residential violent crime may influence tumor biology via reprogramming GR recruitment. Prioritizing lung cancer screening in neighborhoods with increased social stress, such as high levels of violent crime, may reduce racial disparities in lung cancer.
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U2 - 10.1158/2767-9764.CRC-24-0032
DO - 10.1158/2767-9764.CRC-24-0032
M3 - Article
C2 - 38912926
SN - 2767-9764
VL - 4
SP - 1643
EP - 1654
JO - Cancer Research Communications
JF - Cancer Research Communications
IS - 7
ER -