Structural characteristics of small-molecule inhibitors targeting FTO demethylase.
Shuting GaoXitong LiMiao ZhangNing ZhangRui-Yong WangJunbiao ChangPublished in: Future medicinal chemistry (2021)
Studies have shown that the FTO gene is closely related to obesity and weight gain in humans. FTO is an N6-methyladenosine demethylase and is linked to an increased risk of obesity and a variety of diseases, such as acute myeloid leukemia, type 2 diabetes, breast cancer, glioblastoma and cervical squamous cell carcinoma. In light of the significant role of FTO, the development of small-molecule inhibitors targeting the FTO protein provides not only a powerful tool for grasping the active site of FTO but also a theoretical basis for the design and synthesis of drugs targeting the FTO protein. This review focuses on the structural characteristics of FTO inhibitors and discusses the occurrence of obesity and cancer caused by FTO gene overexpression.
Keyphrases
- weight gain
- small molecule
- type diabetes
- squamous cell carcinoma
- insulin resistance
- weight loss
- metabolic syndrome
- acute myeloid leukemia
- body mass index
- protein protein
- genome wide
- birth weight
- cancer therapy
- cardiovascular disease
- high fat diet induced
- cell proliferation
- adipose tissue
- dna methylation
- drug delivery
- young adults
- locally advanced
- squamous cell
- childhood cancer
- genome wide analysis