Cellular senescence molecules expression in type 2 diabetes mellitus: CDKN2A, CDKN2B, and lncRNA ANRIL

被引:1
|
作者
Anaraki, Soheila [1 ]
Kheirandish, Masoumeh [2 ]
Mousavi, Pegah [3 ]
Tamandegani, Atefe Ebrahimi [1 ]
Mohammadi, Samane [1 ]
Shekari, Mohammad [1 ]
机构
[1] Hormozgan Univ Med Sci, Fac Med, Dept Med Genet, Bandar Abbas 7919915519, Iran
[2] Hormozgan Univ Med Sci, Endocrinol & Metab Res Ctr, Bandar Abbas, Iran
[3] Hormozgan Univ Med Sci, Hormozgan Hlth Inst, Mol Med Res Ctr, Bandar Abbas, Iran
关键词
Biomarker; Long noncoding RNA; Cyclin-dependent kinase inhibitor 2A /2B; CDKN2B-AS1; Real-time PCR; Peripheral blood mononuclear cells; INFLAMMATION; DISEASE; CELLS;
D O I
10.1016/j.gene.2024.148319
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Aims: Cellular senescence in type 2 diabetes mellitus (T2DM) has received widespread attention. However, the cellular senescence molecules involved in T2DM are unclear. Furthermore, there are no consistent biomarkers for cellular senescence in T2DM. Therefore, this study aimed to identify cellular senescence molecules in T2DM and investigate their expression in peripheral blood mononuclear cells of individuals with T2DM. Methods: Patients with T2DM (n = 40) and healthy controls (n = 40) were enrolled. We used different databases to identify cellular senescence molecules in T2DM and confirmed the obtained genes and lncRNA using real-time PCR. Results: Bioinformatics analysis indicated that CDKN2A and CDKN2B genes, and long noncoding RNA ANRIL are the most effective cellular senescence molecules in T2DM. Furthermore, CDKN2A and ANRIL expression decreased in individuals with T2DM. Conclusions: Cellular senescence may have a protective effect against T2DM. In addition, the cellular senescence molecules CDKN2A and ANRIL may be potential biomarkers of cellular senescence in T2DM.
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页数:7
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