Melatonin suppresses tumor proliferation and metastasis by targeting GATA2 in endometrial cancer

Author:

Liao Yangyou1,Li Ruiling1,Pei Jingyuan1,Zhang Juan1,Chen Bo1,Dong Haojie1,Feng Xiaoyu1,Zhang Hongshuo1,Shang Yuhong2,Sui Linlin1,Kong Ying1

Affiliation:

1. Core Laboratory of Glycobiology and Glycoengineering, College of Basic Medical Sciences Dalian Medical University Dalian China

2. Department of Gynecology, First Affiliated Hospital Dalian Medical University Dalian Liaoning China

Abstract

AbstractEndometrial cancer (EC) is a reproductive system disease that occurs in perimenopausal and postmenopausal women. However, its etiology is unclear. Melatonin (MT) has been identified as a therapeutic agent for EC; however, its exact mechanism remains unclear. In the present study, we determined that GATA‐binding protein 2 (GATA2) is expressed at low levels in EC and regulated by MT. MT upregulates the expression of GATA2 through MT receptor 1A (MTNR1A), whereas GATA2 can promote the expression of MTNR1A by binding to its promoter region. In addition, in vivo and in vitro experiments showed that MT inhibited the proliferation and metastasis of EC cells by upregulating GATA2 expression. The protein kinase B (AKT) pathway was also affected. In conclusion, these findings suggest that MT and GATA2 play significant roles in EC development.

Publisher

Wiley

Subject

Endocrinology

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