The Novel Link between Gene Expression Profiles of Adult T-Cell Leukemia/Lymphoma Patients' Peripheral Blood Lymphocytes and Ferroptosis Susceptibility

被引:5
作者
Wang, Yu [1 ]
Iha, Hidekatsu [1 ,2 ]
机构
[1] Oita Univ, Fac Med, Dept Microbiol, 1-1 Idaigaoka Hasama, Yufu, Oita 8795593, Japan
[2] Oita Univ, Fac Med, Res Ctr GLOBAL & LOCAL Infect Dis RCGLID, Div Pathophysiol, 1-1 Idaigaoka, Hasama, Yufu, Oita 8795593, Japan
关键词
ferroptosis; adult T-cell leukemia/lymphoma (ATL); bioinformatic analysis; precision medicine; VIRUS TYPE-I; ZINC-FINGER PROTEIN; WEB-BASED TOOL; LEUKEMIA-LYMPHOMA; PHASE-II; INHIBITOR; CANCER; AUTOPHAGY; NETWORK; HTLV-1;
D O I
10.3390/genes14112005
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Ferroptosis, a regulated cell death dependent on iron, has garnered attention as a potential broad-spectrum anticancer approach in leukemia research. However, there has been limited ferroptosis research on ATL, an aggressive T-cell malignancy caused by HTLV-1 infection. Our study employs bioinformatic analysis, utilizing dataset GSE33615, to identify 46 ferroptosis-related DEGs and 26 autophagy-related DEGs in ATL cells. These DEGs are associated with various cellular responses, chemical stress, and iron-related pathways. Autophagy-related DEGs are linked to autophagy, apoptosis, NOD-like receptor signaling, TNF signaling, and the insulin resistance pathway. PPI network analysis revealed 10 hub genes and related biomolecules. Moreover, we predicted crucial miRNAs, transcription factors, and potential pharmacological compounds. We also screened the top 20 medications based on upregulated DEGs. In summary, our study establishes an innovative link between ATL treatment and ferroptosis, offering promising avenues for novel therapeutic strategies in ATL.
引用
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页数:21
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