MiR-125b-5p Targets MTFP1 to Inhibit Cell Proliferation, Migration, and Invasion and Facilitate Cell Apoptosis in Endometrial Carcinoma

被引:5
|
作者
Pan, Shan [1 ]
Zhou, Jianqing [1 ]
Yang, Wenjuan [1 ]
Zhu, Weili [1 ]
Zhu, Tao [2 ]
Yang, Baicai [1 ]
Tang, Xuedong [1 ]
机构
[1] Jiaxing Univ, Dept Obstet & Gynecol, Affiliated Women & Children Hosp, 2468 Zhonghuan East Rd, Jiaxing 314001, Zhejiang, Peoples R China
[2] Zhejiang Canc Hosp, Dept Gynecol, Hangzhou 310022, Zhejiang, Peoples R China
关键词
miR-125b-5p; MTFP1; Endometrial carcinoma; Proliferation; Migration; Invasion; Apoptosis; MITOCHONDRIAL FISSION; HYDROTHERMAL SYNTHESIS; NANOCOMPOSITES; PROGRESSION; MUTATIONS; AUTOPHAGY; SURVIVAL; ALMOND;
D O I
10.1007/s12033-022-00601-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) are recognized as latent diagnostic, prognostic, and therapeutic biomarkers for endometrial carcinoma (EC). We attempted to discuss function and mechanism of miR-125b-5p in EC cell progression. This study manifested a decreased miR-125b-5p level and an increased mitochondrial fission process 1 (MTFP1) level in EC, and there was an inverse correlation between them. Moreover, in vitro assays were performed. The results denoted that miR-125b-5p could target a putative binding site on MTFP1 3'UTR to reduce MTFP1 expression, thereby repressing cell malignant behaviors. Besides, the promoting impact of MTFP1 overexpression on malignant phenotypes of EC cells could be restored by miR-125b-5p up-regulation. Considering, our investigation exhibited that miR-125b-5p curbed EC cell malignant phenotypes through targeting MTFP1. This study generates a fresh functional mechanism for EC occurrence and progression, which also lays the groundwork for clinical therapies.
引用
收藏
页码:961 / 969
页数:9
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