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Therapeutic radiation exposure of the abdomen during childhood induces chronic adipose tissue dysfunction
Xiaojing Huang, Olivia A. Maguire, Jeanne M. Walker, Caroline S. Jiang, Thomas S. Carroll, Ji-Dung Luo, Emily Tonorezos, Danielle Novetsky Friedman, Paul Cohen
Xiaojing Huang, Olivia A. Maguire, Jeanne M. Walker, Caroline S. Jiang, Thomas S. Carroll, Ji-Dung Luo, Emily Tonorezos, Danielle Novetsky Friedman, Paul Cohen
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Clinical Research and Public Health Metabolism Oncology

Therapeutic radiation exposure of the abdomen during childhood induces chronic adipose tissue dysfunction

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Abstract

BACKGROUND Childhood cancer survivors who received abdominal radiotherapy (RT) or total body irradiation (TBI) are at increased risk for cardiometabolic disease, but the underlying mechanisms are unknown. We hypothesize that RT-induced adipose tissue dysfunction contributes to the development of cardiometabolic disease in the expanding population of childhood cancer survivors.METHODS We performed clinical metabolic profiling of adult childhood cancer survivors previously exposed to TBI, abdominal RT, or chemotherapy alone, alongside a group of healthy controls. Study participants underwent abdominal s.c. adipose biopsies to obtain tissue for bulk RNA sequencing. Transcriptional signatures were analyzed using pathway and network analyses and cellular deconvolution.RESULTS Irradiated adipose tissue is characterized by a gene expression signature indicative of a complex macrophage expansion. This signature includes activation of the TREM2-TYROBP network, a pathway described in diseases of chronic tissue injury. Radiation exposure of adipose is further associated with dysregulated adipokine secretion, specifically a decrease in insulin-sensitizing adiponectin and an increase in insulin resistance–promoting plasminogen activator inhibitor-1. Accordingly, survivors exhibiting these changes have early signs of clinical metabolic derangement, such as increased fasting glucose and hemoglobin A1c.CONCLUSION Childhood cancer survivors exposed to abdominal RT or TBI during treatment exhibit signs of chronic s.c. adipose tissue dysfunction, manifested as dysregulated adipokine secretion that may negatively impact their systemic metabolic health.FUNDING This study was supported by Rockefeller University Hospital; National Institute of General Medical Sciences (T32GM007739); National Center for Advancing Translational Sciences (UL1 TR001866); National Cancer Institute (P30CA008748); American Cancer Society (133831-CSDG-19-117-01-CPHPS); American Diabetes Association (1-17-ACE-17); and an anonymous donor (MSKCC).

Authors

Xiaojing Huang, Olivia A. Maguire, Jeanne M. Walker, Caroline S. Jiang, Thomas S. Carroll, Ji-Dung Luo, Emily Tonorezos, Danielle Novetsky Friedman, Paul Cohen

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Figure 2

Gene expression signatures of irradiated adipose tissue.

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Gene expression signatures of irradiated adipose tissue.
(A) Principal c...
(A) Principal component analysis of RNA-seq results. Ellipses show 95% CI. (B–E) Polar-coordinate volcano plots comparing TBI, ABM, CHM; TBI, ABM, CTL; ABM, CHM, CTL; and TBI, CHM, CTL groups. Individual genes are represented as points. Radial coordinates of each gene are calculated based on the gene’s expression Z score in each of the subject groups labeled on the radial axes; proximity to an axis indicates increased expression in the group indicated on that axis. Colored points indicate significantly upregulated genes in the labeled subject groups; significance is determined by a P value cutoff of 0.01 using the likelihood ratio test implemented in DESeq2. (F) Gene ontology (GO) enrichment analysis of genes upregulated in both TBI and ABM groups, scored as –log10 of the adjusted P value from topGO.

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