高胰岛素血症
胰岛素抵抗
癌变
表观遗传学
癌症
生物信息学
生物
DNA甲基化
糖尿病
胰岛素
2型糖尿病
胰腺癌
癌症研究
激素
机制(生物学)
医学
遗传学
内分泌学
基因
基因表达
哲学
认识论
作者
Eusebio Chiefari,Maria Mirabelli,Sandro La Vignera,Sinan Tanyolaç,Daniela Foti,Antônio Aversa,Antonio Brunetti
标识
DOI:10.3390/ijms222011137
摘要
Insulin resistance (IR) is a condition which refers to individuals whose cells and tissues become insensitive to the peptide hormone, insulin. Over the recent years, a wealth of data has made it clear that a synergistic relationship exists between IR, type 2 diabetes mellitus, and cancer. Although the underlying mechanism(s) for this association remain unclear, it is well established that hyperinsulinemia, a hallmark of IR, may play a role in tumorigenesis. On the other hand, IR is strongly associated with visceral adiposity dysfunction and systemic inflammation, two conditions which favor the establishment of a pro-tumorigenic environment. Similarly, epigenetic modifications, such as DNA methylation, histone modifications, and non-coding RNA, in IR states, have been often associated with tumorigenesis in numerous types of human cancer. In addition to these observations, it is also broadly accepted that gut microbiota may play an intriguing role in the development of IR-related diseases, including type 2 diabetes and cancer, whereas potential chemopreventive properties have been attributed to some of the most commonly used antidiabetic medications. Herein we provide a concise overview of the most recent literature in this field and discuss how different but interrelated molecular pathways may impact on tumor development.
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