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The Expression of MBD6 Is Associated with Tumor Size in Uterine Leiomyomas

Authors :
Mei-rong Liang
Yong Luo
Feng Wang
Fa-Ying Liu
Ziyu Zhang
Yang Bicheng
Ouping Huang
Yang Zou
Yang Zeng
Si-Yuan Zeng
Jun-Wen Zhang
Source :
Genetic testing and molecular biomarkers. 23(8)
Publication Year :
2019

Abstract

Background: Uterine leiomyoma (UL) is the most common benign smooth muscle tumor of the uterus in reproductive women. Prior studies indicated that methyl-CpG-binding domain proteins (MBDs) may be involved in the pathogenesis of UL. Materials and Methods: In this study, UL tissues and paired adjacent myometrium were collected from a total of 51 patients. The expression of MBD mRNAs and their cognate proteins were analyzed via quantitative polymerase chain reaction assays and western blotting, respectively. The relationships between the MBD expression levels and the patients' clinicopathologic variables were assessed using Student's t test, nonparametric tests, or Pearson χ2 methods. Results: Our results show that both the mRNA and protein levels of MBD2 were significantly decreased in ULs compared to the adjacent myometrium. In addition, MBD6 protein expression was also decreased significantly in UL samples when compared to the adjacent myometrium. There was, however, no significant difference on the mRNA expression of MBD6 between these two groups. Neither the mRNA nor the protein levels of the other MBD members (MBD1, MBD3, MBD4, MBD5, and MeCP2) showed any significant differences between ULs and the adjacent myometria. The decreased expression of the MBD6 protein was correlated with the tumor size of ULs. Conclusions: These results suggest that the dysregulated expression of MBD2 and MBD6 in ULs may play a role in their development; however, a larger sample size together with cellular functional assays should be carried out to further elucidate the precise role of MBD6 in ULs.

Details

ISSN :
19450257
Volume :
23
Issue :
8
Database :
OpenAIRE
Journal :
Genetic testing and molecular biomarkers
Accession number :
edsair.doi.dedup.....4bcda7f6995f7456b0eb1679d136349b