| Literature DB >> 32934724 |
Nan Mu1, Tingting Xu1, Mingxiao Gao2, Mei Dong2, Qing Tang1, Li Hao1, Guiqing Wang1, Zenghui Li1, Wenshuang Wang1, Ying Yang1, Jianqing Hou1.
Abstract
The present review aims at reviewing the role of metformin in the treatment of endometrial cancer (EC). According to the literature, excessive estrogen levels and insulin resistance are established risk factors of EC. As a traditional insulin sensitizer and newly discovered anticancer agent, metformin directly and indirectly inhibits the development of EC. The direct mechanisms of metformin include inhibition of the LKB1-AMP-activated protein kinase-mTOR, PI3K-Akt and insulin-like growth factor 1-related signaling pathways, which reduces the proliferation and promotes the apoptosis of EC cells. In the indirect mechanism, metformin increases the insulin sensitivity of body tissues and decreases circulating insulin levels. Decreased levels of insulin increase the blood levels of sex hormone binding globulin, which leads to reductions in circulating estrogen and androgens. The aforementioned findings suggest that metformin serves an important role in the treatment of EC. Increased understanding of the mechanism of metformin in EC may provide novel insights into the treatment of this malignancy.Entities:
Keywords: endometrial cancer; insulin resistance; medical treatment; metformin; signaling pathway
Year: 2020 PMID: 32934724 PMCID: PMC7471738 DOI: 10.3892/ol.2020.12017
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967