Author:
Ju Sang-Hyeon,Lee Seong Eun,Yi Shinae,Choi Na Rae,Kim Kun Ho,Kim Seong Min,Koh June-Young,Kim Seon-Kyu,Kim Seon-Young,Heo Jun Young,Park Junyoung O.,Park Seongyeol,Koo Bon Seok,Kang Yea Eun
Abstract
AbstractThe SUVmax is a measure of FDG uptake and is related with tumor aggressiveness in thyroid cancer, however, its association with molecular pathways is unclear. Here, we investigated the relationship between SUVmax and gene expression profiles in 80 papillary thyroid cancer (PTC) patients. We conducted an analysis of DEGs and enriched pathways in relation to SUVmax and tumor size. SUVmax showed a positive correlation with tumor size and correlated with glucose metabolic process. The genes that indicate thyroid differentiation, such as SLC5A5 and TPO, were negatively correlated with SUVmax. Unsupervised analysis revealed that SUVmax positively correlated with DNA replication(r = 0.29, p = 0.009), pyrimidine metabolism(r = 0.50, p < 0.0001) and purine metabolism (r = 0.42, p = 0.0001). Based on subgroups analysis, we identified that PSG5, TFF3, SOX2, SL5A5, SLC5A7, HOXD10, FER1L6, and IFNA1 genes were found to be significantly associated with tumor aggressiveness. Both high SUVmax PTMC and macro-PTC are enriched in pathways of DNA replication and cell cycle, however, gene sets for purine metabolic pathways are enriched only in high SUVmax macro-PTC but not in high SUVmax PTMC. Our findings demonstrate the molecular characteristics of high SUVmax tumor and metabolism involved in tumor growth in differentiated thyroid cancer.
Funder
National Research Foundation of Korea
Ministry of Trade, Industry, and Energy (MOTIE), Korea
Korea Health Technology R&D Project through the Korea Health Industry Development Institute
Chungnam National University Hospital Research Fund, 2021
Publisher
Springer Science and Business Media LLC